Aphasia research studies


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ehoover@bu.edu, gayle.dede@temple.edu

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Dear Elizabeth Hoover and Gayle DeDe,

I found your research on aphasiaresearch.org.
I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
The best way to contact me is:
  Caregiver: [Insert your phone / email]
  Person with aphasia: [Insert your phone / email]
Thank you for doing this research.

Sincerely,
[Insert your name]

Conversation Group Treatment for Aphasia: Does it Work?

Principle Investigator: NA
Institution: Boston University Charles River Campus
Country: United States
City: Boston, Massachusetts; Maywood, New Jersey; Philadelphia, Pennsylvania

Brief Description:

The proposed research will test the efficacy of group conversation treatment for people with aphasia and explore whether the effects of treatment differ as a result of the following factors:

Group size: Do large groups of 6-8 people with aphasia or dyads of 2 people with aphasia demonstrate different levels of improvement with this treatment? Group composition: Do effects of conversation group treatment differ if the groups include members with similar or different types of aphasia? Aphasia severity: Do effects of conversation group treatment differ if the individuals within the group have mild-moderate or moderate-severe profiles of aphasia?

Treatment sessions will occur in groups of 6-8 people with aphasia or with 2 people with aphasia. During treatment sessions, discourse will be facilitated on a focused set of every day topics, such as current events or travel. Linguistic and multi modal cueing hierarchies will be tailored to individual client goals and used to maximize communication success.

The prediction is that conversation treatment is an effective method for improving communication in people with aphasia, but that specific benefits may differ based on variables such as group size, group composition, and aphasia severity. The results will help inform best practices for aphasia treatment and refine a hypothesized model about the mechanisms underlying conversation treatment.

Inclusion Criteria:
Criteria for All Treatment Cycles
  • :
  • Clinical diagnosis of aphasia
  • At least 6 months post-onset of stroke in the language-dominant hemisphere.
  • Native English speakers
  • Demonstrate sufficient auditory comprehension skills to participate in a supported conversation, based on results of standardized aphasia tests
  • Exclusion
  • No history of neurological disease (other than stroke)
  • No history of developmental speech, language, or learning disabilities
  • No current serious medical illness (e.g., cancer)
  • Participants will be asked to abstain from concurrent speech language treatment.
  • Separate criteria for Treatment Cycles 1, 2, and 3 based on aphasia severity:
  • Cycle 1 Severity-based Inclusion Criteria (Planned 2022):
  • – All aphasia profiles and severity levels.
  • Cycle 2 Severity-based Inclusion Criteria (Planned 2023):
  • – Participants with severe aphasia
  • Cycle 3 Severity-based Inclusion Criteria (Planned 2024):
  • – Participants with mild-moderate aphasia.
  • Exlcusion Criteria:
    NA

    Contact Information:
    Elizabeth Hoover, PhD
    Phone:
    1. 353-8967
    Email:
    Gayle DeDe, PhD
    Phone:
    1. 204-2453
    Email:
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    sharon.antonucci@jefferson.edu, sharon.antonucci@jefferson.edu

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    Dear Sharon M. Antonucci and Steph Wolfert,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Assessing an Animal-Assisted Treatment Program for Adults With Aphasia: The Persons With Aphasia Training Dogs Program

    Principle Investigator: Sharon Antonucci, PhD
    Institution: Albert Einstein Healthcare Network
    Country: United States
    City: Elkins Park, Pennsylvania

    Brief Description:
    The lives of more than 2 million Americans are affected by aphasia, an acquired language impairment most commonly resulting from stroke that affects the ability to remember and express words. The well-being of these individuals is affected not just by the loss of words that is aphasia, but also the loss of friendships and opportunities for community engagement in which the loss of words can result. This study evaluates an animal-assisted treatment, The Persons with Aphasia Training Dogs (PATD) Program, designed to target the psychosocial consequences of aphasia by training participants in positive reinforcement dog training techniques that harness new skill learning and the advantages of interaction with family- or shelter-dwelling dogs to increase confidence and social engagement to support participants in living well with aphasia.

    Inclusion Criteria:
  • Clinical diagnosis of aphasia acquired as the result of cerebro-vascular accident (CVA)
  • English as a native or primary language
  • Evidence of linguistic and cognitive capacity to understand the research requirements
  • Willingness and stamina to participate in the protocol
  • Lives within 1 hour driving distance to MRRI (50 Township Line Rd, Elkins Park, PA 19027 and (as appropriate) PSPCA HQ (350 E. Erie Ave., Philadelphia, PA 19134
  • Exlcusion Criteria:
  • • Diagnosis of neurological injury or disease other than CVA

  • Contact Information:
    Sharon M. Antonucci, Ph.D.
    Phone: 215-663-6145
    Email:
    Steph Wolfert
    Phone: 215-663-6145
    Email:
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    marika.schutz@uu.se

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    Dear Marika J Schütz,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Changes in Neuroplasticity Following Intensive Rehabilitation of Aphasia and/or Apraxia of Speech

    Principle Investigator: Ellika Schalling
    Institution: Karolinska Institutet
    Country: Sweden
    City: Uppsala

    Brief Description:
    The present study aims to investigate the short- and long-term effects of two weeks of intensive speech-language pathology intervention with additional physiotherapy, on aphasia and apraxia of speech (AOS) and their neural correlates in thirty persons with chronic stroke. Changes are studied following intensive treatment of aphasia and AOS with standardised speech-language testing and testing of communication and with voxel-based morphometry (VBM) analysis and resting state functional connectivity (rsFC).

    Inclusion Criteria:
  • Aphasia 7 months post stroke diagnosed by SLP
  • Apraxia of Speech 7 months post stroke diagnosed by SLP
  • Exlcusion Criteria:
  • Dementia
  • Severe loss of sight
  • Severe loss of hearing
  • Metal implants (preventing fMRI)
  • Claustrophobia (preventing fMRI)

  • Contact Information:
    Marika J Schütz, Ph.D student
    Phone: 0046737570430
    Email:
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    ssayers@mailbox.sc.edu, KELLIAP@mailbox.sc.edu

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    Dear Sara Sayers and Kelli Powell,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Telerehabilitation for Aphasia (TERRA)

    Principle Investigator: Julius Fridriksson
    Institution: University of South Carolina
    Country: United States
    City: Columbia, South Carolina

    Brief Description:
    Speech-language therapy is generally found to be helpful in the rehabilitation of aphasia. However, not all patients with aphasia have access to adequate treatment to maximize their recovery. The goal of this project is to compare the efficacy of telerehabilitation or Aphasia Remote Therapy (ART) to the more traditional In-Clinic Therapy (I-CT).

    Inclusion Criteria:
  • Participants must have sustained a left hemisphere ischemic or hemorrhagic stroke at least 12 months prior to enrollment.
  • Participants must primarily speak English for at least the past 20 years.
  • Participants must be capable of giving informed consent or indicating another to provide informed consent.
  • Participants must be between 21-80 years of age.
  • Participants must be magnetic resonance imaging (MRI) compatible (e.g., no metal implants, not claustrophobic) on a 3-Tesla (3T) scanner.
  • Exlcusion Criteria:
  • Participants must not have previous neurological disease affecting the brain (e.g. history of traumatic brain injury).
  • Participants must not have severely limited speech production (severe unintelligibility) and/or auditory comprehension that interferes with adequate participation in the therapy provided (i.e., WAB-R Spontaneous Speech rating scale score of 0-1 or WAB-R Comprehension score of 0-1).
  • Participants must not have a history of stroke to the right hemisphere of the brain.
  • Participants must not have a bilateral, cerebellar or brainstem stroke.
  • Participants must not have anything that makes them be 3T MRI incompatible
  • Insufficient intelligible speech to provide accurate responses with discourse/naming.

  • Contact Information:
    Kelli Powell, B.S.
    Phone: 803-777-2693
    Email:
    Sara Sayers, M.S.
    Phone: 803-777-5051
    Email:
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    nmartin@temple.edu, wendy.greenspan@temple.edu

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    Dear Nadine Martin and Wendy Greenspan,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Translation and Clinical Implementation of a Test of Language and Short-term Memory in Aphasia

    Principle Investigator: Nadine Martin
    Institution: Temple University
    Country: United States
    City: Philadelphia, Pennsylvania; Seattle, Washington

    Brief Description:
    This project aims to develop a clinically feasible version of a laboratory-developed assessment battery for language and verbal short-term memory difficulties in aphasia.

    Inclusion Criteria:
  • . single or multiple left hemisphere lesions
  • at least one year post-stroke.
  • high-school educated
  • negative histories for mental illness and alcohol/substance abuse.
  • passed an audiometric pure-tone, air conduction screening at 25 dB HL at 1K, 2K and 4K Hz for at least one ear.
  • Exlcusion Criteria:
  • English as a second language Right hemisphere stroke Less than 6 months post-onset of stroke.

  • Contact Information:
    Nadine Martin, Ph.D.
    Phone: 215 294 1870
    Email:
    Wendy Greenspan, MA
    Phone: 215-204-1790
    Email:
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    ivanova@berkeley.edu

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    Dear Maria Ivanova,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Effects of High-intensity Exercise Training on Physical Fitness, Cognition, Language in Post-stroke Aphasia

    Principle Investigator: Maria Ivanova
    Institution: University of California, Berkeley
    Country: United States
    City: Berkeley, California; Hayward, California; San Francisco, California; San Francisco, California

    Brief Description:

    The goal of this clinical trial is to establish the feasibility and fidelity of a high-intensity exercise program for individuals with post-stroke aphasia. The main questions it aims to answer are:

    Is it feasible for stroke survivors with aphasia to participate in a long in-person physical exercise program? Does participation in a physical exercise program lead to physical fitness, cognitive, language and/or psychological changes?

    Participants can take part in two different physical exercise interventions:

    Low intensity intervention (control intervention); High-intensity physical exercise intervention (target intervention).

    Inclusion Criteria:
  • aphasia following left hemisphere ischemic or hemorrhagic stroke;
  • at least 6 months from the last stroke;
  • proficient in English before the stroke;
  • at least 8 years of education;
  • between the ages of 18 and 80;
  • independent with ambulation without a device (single-point cane accepted);
  • medically stable with no contraindications to participate in regular physical exercise as determined by the patient’s own primary care provider or other treating provider.
  • Exlcusion Criteria:
  • prior history of dementia, neurologic illness (other than stroke), or substance abuse;
  • significant visual or hearing disabilities (e.g., neglect, uncorrected visual or hearing loss) that interfere with testing;
  • per self-report uncontrolled cardiorespiratory and/or metabolic disorders incompatible with exercise.

  • Contact Information:
    Maria Ivanova, PhD
    Phone: 4156389880
    Email:
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    ruiqipanedu@163.com

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    Dear Ruiqi Pan,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    pBFS-guided cTBS at Different Doses for Aphasia After Stroke

    Principle Investigator: NA
    Institution: Changping Laboratory
    Country: China
    City: Nanyang, Henan; Zhengzhou, Henan

    Brief Description:
    The objective of this trial is to evaluate the effectiveness and safeness of different doses of continuous Theta Burst Stimulation (cTBS) over the right Superior Frontal Gyrus (SFG), guided by personalized Brain Function Sector (pBFS) technology, on language function recovery in patients with post-stroke aphasia.

    Inclusion Criteria:
  • The patient’s age ranges from 35 to 75 years old (including 35 and 75 years old);
  • Meet the diagnostic criteria for ischemic stroke (according to the guidelines developed by the American Heart Association/American Stroke Association in 2019 and the guidelines developed by the Neurology Branch of the Chinese Medical Association in 2018) or meet the diagnostic criteria for hemorrhagic stroke (according to the guidelines developed by the American Heart Association/American Stroke Association in 2022 and the guidelines developed by the Neurology Branch of the Chinese Medical Association in 2019) ,with lesions located in the left hemisphere, and a duration of illness ranging from 15 days to 6 months.
  • Diagnosed as aphasia patient according to the Chinese version of Western Aphasia Battery (WAB), with a WAB-aphasia quotient of less than 93.8 points;
  • First onset of stroke;
  • Normal language function before the onset of stroke, and the patient’s native language is Chinese with at least 6 years of education;
  • Understand the trial and signed the informed consent form.
  • Exlcusion Criteria:
  • Combined dysarthria (NIHSS item 10 score ≥2 points);
  • Aphasia caused by bilateral hemisphere stroke, brain tumor, traumatic brain injury, Parkinson’s disease, motor neuron disease, or other diseases;
  • Patients with implanted electronic devices such as cardiac pacemakers, cochlear implants, or other metal foreign bodies, or those with MRI contraindications such as claustrophobia or TMS treatment contraindications;
  • History of epilepsy;
  • Patient with concomitant severe systemic diseases affecting the heart, lungs, liver, kidneys, etc., and uncontrolled by conventional medication, as detected and confirmed through laboratory testing and examination;
  • Patients with consciousness disorders (NIHSS 1(a) score ≥1);
  • Patients with malignant hypertension;
  • Patients with severe organic diseases, such as malignant tumors, with an expected survival time of less than 1 year;
  • Patients with severe hearing, visual, cognitive impairment or inability to cooperate with the trial;
  • Patients with severe depression, anxiety, or diagnosed with other mental illnesses that prevent them from completing the trial;
  • Patients who have received other neuromodulation treatments such as TMS, transcranial electric stimulation, etc. in the 3 months prior to enrollment;
  • Patients with a history of alcoholism, drug abuse, or other substance abuse;
  • Patients with other abnormal findings that the researchers judge are not suitable for participation in this trial;
  • Patients who are unable to complete follow-up due to geographical or other reasons;
  • Women of childbearing age who are currently pregnant, breastfeeding, or planning or may become pregnant during the trial;
  • Patients who are currently participating in other clinical trials.

  • Contact Information:
    Ruiqi Pan
    Phone: 010-80726688
    Email:
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    svallilarohter@mghihp.edu, mlnicholas@mghihp.edu

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    Dear Sofia Vallila Rohter and Marjorie Nicholas,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Incorporating Strategy Training Into Naming Treatment in Aphasia

    Principle Investigator: Sofia Vallila Rohter
    Institution: MGH Institute of Health Professions
    Country: United States
    City: Boston, Massachusetts

    Brief Description:

    This study incorporates metacognitive strategy training into semantic feature analysis treatment. Semantic feature analysis treatment has a strong evidence base and capacity to improve word retrieval by encouraging circumlocution. Circumlocution facilitates self-cued naming and assists listener comprehension when naming fails. However, semantic feature analysis treatment does not include direct techniques to teach patients with aphasia to generalize the use of semantic feature analysis treatment’s circumlocution procedure. Therefore, this study proposes that combining semantic feature analysis treatment and metacognitive strategy training will stimulate the semantic system and increase patients with aphasias’ use of circumlocution across divergent contexts.

    This study aims to measure the treatment’s effect on naming accuracy for trained and untrained items. The study also aim to measure the treatment’s effect on people with aphasias’ knowledge of the strategy components and changes in verbalizations during retrieval attempts. The central hypothesis is that strategy training will increase patients with aphasias’ explicit knowledge about circumlocution and enable them to use it to (1) self-facilitate naming, and (2) produce more informative connected speech.

    Inclusion Criteria:
  • Experienced a single left-hemisphere stroke,
  • Have aphasia due to stroke,
  • Be in the chronic stages of their aphasia, at least 6 months post onset of stroke.
  • Be between the ages of 18 and 89 years of age, and
  • Be a proficient English speaker,
  • Have no history of neurodegenerative disease, motor speech disorder, significant mental illness, psychiatric disorder, drug/alcohol abuse, or neurological condition that could influence their cognitive, language, and memory systems.
  • Exlcusion Criteria:
  • Experienced multiple strokes;
  • Be in the acute stage of their aphasia, <6 months post onset of stroke;
  • Have a diagnosis of neurodegenerative disease, significant mental illness, psychiatric disorder, drug/alcohol abuse, or neurological condition that could influence cognitive, language, and memory systems

  • Contact Information:
    Marjorie Nicholas, PhD
    Phone: 617-724-3824
    Email:
    Sofia Vallila Rohter, PhD
    Phone: 617-726-0685
    Email:
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    cute@musc.edu, krajeck@musc.edu

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    Dear Stephanie Cute and Kelly Krajeck,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Speech Entrainment for Aphasia Recovery

    Principle Investigator: Leonardo Bonilha
    Institution: Medical University of South Carolina
    Country: United States
    City: Charleston, South Carolina; Columbia, South Carolina; Salt Lake City, Utah

    Brief Description:

    After a stroke, many people experience a language impairment called aphasia. One of the most debilitating types of aphasia is non-fluent aphasia. Non-fluent aphasia is defined by significantly reduced speech production, with the speaker producing only a few words or even less. Speech entrainment therapy (SET) is a treatment that has been shown to increase fluency in people with non-fluent aphasia. The study looks to define the best dose of SET that leads to sustained improvements in spontaneous speech production.

    Participants who are eligible will undergo baseline language testing, an MRI, and will be randomized into one of 4 treatment groups: SET for 3 weeks, SET for 4.5 weeks, SET for 6 weeks, and no treatment (control group).

    Inclusion Criteria:
  • Aphasia as a result of a left hemisphere ischemic or hemorrhagic stroke (WAB-R Aphasia Quotient <93.8).
  • Presence of left hemisphere stroke in clinical imaging (CT/MRI) and NIHSS
  • Participants must have spoken English as their primary language.
  • 21-81 years old
  • Pre-stroke modified Rankin Scale (mRS)= 2 or less
  • Post-stroke mRS= 4 or less.
  • At least 6 months post-stroke.
  • Non-fluent aphasia (WAB-R Comprehension score >4 and WAB-R Fluency score <6).
  • Technological compatibility (to be determined by clinical judgment of SLP)
  • Exlcusion Criteria:
  • History of chronic neurological or psychiatric diseases (excluding migraines, depression, or post-stroke epilepsy). Self-reported history of learning disability.
  • Severe dysarthria (determined via SLP clinical judgment from spontaneous speech tasks on the ASRS 3.0).
  • Global aphasia.
  • History of right-hemisphere strokes or brain stem/cerebellar strokes with persistent deficits (as evidenced by MRI/CT and NIHSS).
  • Uncorrectable hearing as determined by the SLP’s clinical judgment.
  • Uncorrectable vision.
  • Contraindications to MRI or inability to complete the MRI scanning session.
  • Women who are pregnant.

  • Contact Information:
    Kelly Krajeck, MHA
    Phone:
    1. 792-3678
    Email:
    Stephanie Cute, CCC-SLP
    Phone:
    1. 792-0189
    Email:
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    jianting.huang@pku.edu.cn, ruiqipanedu@163.com

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    Dear Jianting Huang and Ruiqi Pan,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    pBFS-guided cTBS Over the Inferior Frontal Gyrus for Aphasia After Ischemic Stroke

    Principle Investigator: NA
    Institution: Changping Laboratory
    Country: China
    City: Fuzhou, Fujian

    Brief Description:
    The objective of this trial is to evaluate the effectiveness and safeness of continuous Theta Burst Stimulation (cTBS) over the right Inferior Frontal Gyrus (IFG), guided by personalized Brain Functional Sector (pBFS) technology, on language function recovery in patients with post-ischemic stroke aphasia.

    Inclusion Criteria:
  • Patients between the ages of 35 and 75 years (including 35 and 75 years).
  • Meet the diagnostic criteria of acute ischemic stroke (using the 2019 American Heart Association/American Stroke Association Guidelines for the Early Management of Patients With Acute Ischemic Stroke: 2019 Update to the 2018 Guidelines for the Early Management of Acute Ischemic Stroke and the 2018 Chinese Society of Neurology Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke in China). All lesions should be in the left hemisphere, and the course of disease should be more than or equal to 15 days and less than or equal to 3 months .
  • Meet the diagnostic criteria for aphasia according to the Chinese version of the Western Aphasia Battery (WAB), with a WAB-aphasia quotient less than 93.8.
  • First onset stroke.
  • Normal functioning language abilities before the stroke, with Mandarin as their native language and an educational level higher than primary school (more than 6 years’ education).
  • Understand the trial and be able to provide informed consent.
  • Exlcusion Criteria:
  • Combined severe dysarthria (NIHSS item 10 score ≥ 2 points);
  • Aphasia caused by bilateral hemispheric stroke, brain tumors, traumatic brain injury, Parkinson’s disease, motor neuron disease, or other diseases;
  • Patients with implanted electronic devices such as cardiac pacemakers, cochlear implants, or other metal foreign bodies, or those with MRI contraindications such as claustrophobia or TMS treatment contraindications;
  • History of epilepsy;
  • Patients with severe systemic diseases such as heart, lung, liver, kidney diseases, etc., which cannot be controlled by routine medications as confirmed by laboratory tests and examinations;
  • Impaired consciousness (NIHSS item 1(a) score ≥ 1 point);
  • Malignant hypertension;
  • Malignant tumor;
  • Patients with a life expectancy of less than 1 year due to reasons other than stroke;
  • Severe hearing, visual, or cognitive impairments that prevent the patient from completing the trial;
  • Patients with severe depression, anxiety, or other mental illnesses that prevent them from completing the trial;
  • Patients who have received other neuroregulatory treatments such as TMS or transcranial electrical stimulation within 3 months before enrollment;
  • History of alcohol abuse, drug abuse, or other substance abuse;
  • Patients with other abnormal test results that make them unsuitable for participating in this trial as determined by the researchers;
  • Women of childbearing age who are pregnant or planning to become pregnant;
  • Patients participating in other clinical trials.

  • Contact Information:
    Jianting Huang, MD,PhD
    Phone: 010-80726688
    Email:
    Ruiqi Pan
    Phone: 010-80726688
    Email:
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    pytsai@vghtpe.gov.tw

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    Dear Po-Yi Tsai,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Establishment of Virtual Reality System for Stroke Patients With Aphasia

    Principle Investigator: NA
    Institution: Taipei Veterans General Hospital, Taiwan
    Country: Taiwan
    City: Taipei city

    Brief Description:
    Aphasia can significantly influence a person’s social relationship and quality of life. To achieve positive language outcomes, an intensive and high-repetition speech therapy is essential. However, due to the limited number of speech therapists, the intensity and frequency of training are often insufficient. Therefore, it is critical to develop other rehabilitation approaches to enhance the benefits of aphasia intervention. Virtual reality (VR) is an immersive and interactive computer simulation technology that can promote the ecological validity of speech therapy. In this study, we develop an innovative VR software for speech training to explore the effects of VR on various aspects of language outcomes.

    Inclusion Criteria:
  • Diagnosis of stroke with aphasia, including fluent and non-fluent types
  • Age between 20~80-year-old
  • Able to understand virtual reality training
  • Able to cooperate with instructions and follow the rules
  • Able to use the virtual reality controller and device
  • Able to sign the subject’s informed consent
  • Exlcusion Criteria:
  • Diagnosis of brain pathology other than stoke, such as brain tumor, Parkinson’s disease, dementia
  • Unable to cooperate with the instructions
  • Unable to learn how to use the virtual reality controller and device
  • Any medical diseases or unstable vital signs that may cause safety concern
  • Severe hearing or vision impairments
  • Have ever received any form of speech therapy or virtual reality training

  • Contact Information:
    Po-Yi Tsai, MD
    Phone: 886-2-2871-2121
    Email:
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    tbulut@medipol.edu.tr, tbulut@medipol.edu.tr

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    Dear Talat Bulut and MEDKOM,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Efficacy of Low-frequency rTMS in Aphasia

    Principle Investigator: Talat Bulut
    Institution: Medipol University
    Country: Turkey
    City: Istanbul

    Brief Description:

    In a randomized controlled trial, efficacy of low-frequency, inhibitory rTMS will be examined in rehabilitation of acquired aphasia. Two cortical sites will be targeted: Right-hemispheric homologues of Broca’s and Wernicke’s areas.

    In addition to cognitive screening prior to onset of rTMS, language assessments will be conducted before, during and after the intervention. An eyetracking-while-listening experiment will also be conducted before and after the intervention to investigate morphosyntactic processing.

    Inclusion Criteria:
  • Right-handedness,
  • Normal or corrected-to-normal vision and hearing,
  • Aphasia following cerebrovascular accident,
  • Cerebrovascular accident at least 6 months prior to enrolment in the study,
  • Satisfying current TMS safety guidelines (Rossi et al. 2009, 2021), which are:
  • No previous history of epilepsy,
  • No implant (e.g., cochlear implant) or stimulator (e.g., deep brain stimulation) in the head which may interact with the magnetic field,
  • No use of central nervous system active drugs that lower seizure threshold (as listed in the aforementioned guidelines)
  • Exlcusion Criteria:
  • Left-handedness, ambidexterity,
  • Impaired and uncorrected vision or hearing,
  • No aphasia symptoms following cerebrovascular accident,
  • Time since cerebrovascular accident less than 6 months,
  • Violating current TMS safety guidelines (Rossi et al. 2009, 2021). In other words:
  • Having a previous history of epilepsy,
  • Having an implant (e.g., cochlear implant) or stimulator (e.g., deep brain stimulation) in the head which may interact with the magnetic field,
  • Taking central nervous system active drugs that lower seizure threshold (as listed in the aforementioned guidelines)

  • Contact Information:
    MEDKOM
    Phone: +905313327754
    Email:
    Talat Bulut, Ph.D.
    Phone: +90 444 85 44
    Email:
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    Fazaila.ehsan@riphah.edu.pk, Nazia.mumtaz@riphah.edu.pk

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    Dear Fazaila Ehsan and Nazia Mumtaz,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Effect of Communication Partner Training Program for the Management of Persons With Aphasia

    Principle Investigator: NA
    Institution: Riphah International University
    Country: Pakistan
    City: Lahore, Punjab

    Brief Description:
    Communication Partner Training (CPT) is an evidence-based intervention that teaches communication partners (e.g., family members, friends, healthcare workers) how to best support conversation and interaction for a person with aphasia. It does not matter how mild or severe a person’s aphasia is, they can be a good candidate for CPT as long as their communication partner is motivated and willing to adapt their communication style. The objective of this study is to see the effects of communication partner training for the management of persons with aphasia. A randomized controlled trial will be conducted. In total, 6 dyads will be randomly assigned to the intervention (CPT program) or usual care (control) group. Statistical Package for Social Sciences (SPSS) V 25. will be used for Data analysis. Results will be extracted. Conclusion will be made after comparing the pre and post treatment results on person with aphasia.

    Inclusion Criteria:
  • The participant’s aphasia must be caused by stroke and to have occurred at least 12 months before the study takes place.
  • The participant’s aphasia could be of all degrees of severity (clinically assessed as mild, moderate, or severe on GCS).
  • The participants with aphasia are required to be 18 years or older, living at home or planned to live at home after rehabilitation, and have no other speech or language impairments (such as severe dysarthria)
  • Others have to communicate with the person with aphasia on a regular basis (at least once a week).
  • Exlcusion Criteria:
  • The participants will be excluded if the persons with aphasia:
  • Are diagnosed with dementia or any other known significant cognitive impairment.
  • Have significant hearing or vision problems.
  • Have known alcohol or drug abuse.

  • Contact Information:
    Fazaila Ehsan, PhD*
    Phone: 0320-4587164
    Email:
    Nazia Mumtaz, PhD
    Phone: 0333-5196500
    Email:
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    kpolanowska@ipin.edu.pl, iwanski@ipin.edu.pl

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    Dear Katarzyna E Polanowska and Szczepan Iwański,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Effects of Neuronavigated Theta Burst Stimulation in Therapy of Post-stroke Aphasia

    Principle Investigator: Katarzyna Polanowska
    Institution: Institute of Psychiatry and Neurology, Warsaw
    Country: Poland
    City: Warsaw, Masovian Voivodeship

    Brief Description:
    Aphasia is an impairment in the ability to express and/or understand language, commonly observed after stroke to the language dominant (left) hemisphere. Despite natural tendency to spontaneous functional recovery in the first months post stroke and language improvement due to application of behavioral speech and language therapy (SLT), many aphasic patients do not achieve satisfactory level of verbal communication. The aim of the planned study is to explore the potential of the noninvasive repetitive Transcranial Magnetic Stimulation (rTMS) as a therapeutic tool for aphasia in addition to traditional behavioral therapy. In case of aphasia, studies on therapeutic effectiveness of rTMS aim to increase the activity of the language-dominant left cerebral hemisphere, which may be achieved in an indirect manner by inhibiting the activity of the opposite (right) hemisphere or in a direct manner by increasing the excitability of preserved language areas in the left hemisphere. In our study, we plan to administer the newest form of rTMS called Theta Burst Stimulation (TBS), which is safer than the conventional rTMS, even when used in the perilesional area. Computer-based neuronavigation system will be implemented to precisely localize stimulation targets, control administration of stimuli during rTMS sessions, and evaluate differences between participants regarding deviations from established stimulation points. 45 patients (all right-handed, polish native speakers, aged 18-75 years, diagnosed with non-fluent aphasia) will be enrolled in a randomized, double-blind, sham-controlled trial. Subjects will be randomly assigned to one of the three groups: 1) a group with excitatory intermittent TBS of the left hemisphere (iTBS group), 2) a group with inhibitory continuous TBS of the right hemisphere (cTBS group), 3) a group with sham TBS (sTBS group as a control group). Specific forms of stimulation will be carried out for three consecutive weeks (Monday to Friday; a total of 15 stimulation sessions). Immediately after each session of the stimulation, patients will undergo individual SLT. Assessment of language functioning will be carried out three times: before and after the therapy period, and 3 months after its completion. Results of the study will broaden knowledge about hemispherical mechanisms of language and speech recovery after stroke and provide insight into possibilities of their modulation for the purpose of post-stroke rehabilitation.

    Inclusion Criteria:
  • First-ever left middle cerebral artery ischemic stroke (brain damage localization confirmed by magnetic resonance imaging, MRI)
  • 3 or more months from the onset of stroke
  • Non-fluent aphasia (confirmed in the BDAE test) with functional communication difficulties ranging from mild to significant (grades from 2 to 4 in ASRS), marked difficulties in naming, and relatively preserved everyday speech comprehension
  • Native Polish speaker
  • Right-handedness prior to stroke
  • Signing of the informed consent for the participation in the study.
  • Exlcusion Criteria:
  • Psychiatric and/or neurological comorbidity (e. g. dementia, depressive disorder, alcohol dependence)
  • Diagnose of epilepsy or epileptic changes in EEG, also frequent losses of consciousness of unclear etiology which might suggest epileptic seizures
  • History of any neurosurgical procedure around the head area
  • 1.5 T MRI examination contraindications (metal elements in the body, e. g. implantable cardioverter-defibrillator, deep brain stimulation devices; claustrophobia)
  • Regular intake of medication that could affect cortical excitability (e. g. antiepileptic or antipsychotic drugs, antidepressants, benzodiazepines) or medication influencing neuroplastic processes (e. g. dopamine)
  • Significant cognitive impairment limiting patient’s cooperation during assessment and behavioral aphasia therapy
  • Visual deficits significantly hindering the perception of therapeutic tasks presented visually on a computer’s screen
  • New neurological episode (e. g. another brain stroke) or somatic illness (e. g. COVID-19) during the cycle of the therapy, requiring its interruption.

  • Contact Information:
    Katarzyna E Polanowska, PhD
    Phone: +48224582870
    Email:
    Szczepan Iwański, PhD
    Phone: +48224582870
    Email:
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    olsonac@bham.ac.uk

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    Dear Andrew Olson,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Efficacy of Language Games as Therapy for Post Stroke Aphasia

    Principle Investigator: NA
    Institution: University of Birmingham
    Country: United Kingdom
    City: Birmingham, West Midlands

    Brief Description:
    Aphasia is a language impairment experienced by about one third of stroke patients. This often devastating condition is treated by speech and language therapists (SLTs). There is evidence that language games delivered at the right intensity are an efficacious means of improving communication for people with post stroke aphasia. However, it is unclear which mechanism of language facilitation used in a game works best. This study will provide evidence for the “active ingredient” of a game, together with measures of efficacy, feasibility and enjoyment compared to standard aphasia therapy.

    Inclusion Criteria:
  • Adults who have suffered a stroke a minimum of 2 months prior to commencement of the intervention. They will present with expressive aphasia, with relatively preserved language comprehension. They will have been fully fluent in English before the stroke.
  • Exlcusion Criteria:
  • Severe perceptual or cognitive deficits. History of other neurological, psychiatric or neurodegenerative disease impairing language or communicative ability. Severe visual agnosia. Severe limb apraxia. Severe dysarthria. Drug or alcohol abuse.

  • Contact Information:
    Andrew Olson, PhD
    Phone: +44 121 414 3328
    Email:
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    lee1704@purdue.edu, lee1704@purdue.edu

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    Dear Jiyeon Lee and Jiyeon Lee,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Sentence Production Training in Aphasia

    Principle Investigator: Ji Yeon Lee
    Institution: Purdue University
    Country: United States
    City: West Lafayette, Indiana

    Brief Description:
    This study focuses on developing a novel treatment for sentence production and comprehension in aphasia, using implicit priming. First set of experiments will aim examine which priming conditions are most effective in creating maximal learning effects. Then, in a later experiment, the investigators will develop and test the efficacy of a novel treatment study based on findings from the first set of the experiments.

    Inclusion Criteria:
  • Individuals with post-stroke aphasia
  • At least 6 months post-onset of eft hemisphere stroke
  • Native speaker of English
  • Normal or corrected to normal hearing and vision
  • High-school educated
  • Difficulty communicating in sentences, with some ability to use words independently
  • Exlcusion Criteria:
  • Severe apraxia of speech
  • Other neurological conditions affecting communication (e.g., dementia)
  • Uncontrolled psychiatric/psychological conditions affecting thinking and communication
  • Active alcohol/substance abuse

  • Contact Information:
    Jiyeon Lee
    Phone: 7654943810
    Email:
    Jiyeon Lee, PhD
    Phone: 7654943810
    Email:
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    claudia.repetto@unicatt.it, alice.cancer@unicatt.it

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    Dear Claudia Repetto and Alice Cancer,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Virtual Reality Training for Aphasia Rehabilitation

    Principle Investigator: Claudia Repetto
    Institution: Catholic University of the Sacred Heart
    Country: Italy
    City: Brescia

    Brief Description:
    Aphasia is an acquired deficit following acute damage to the central nervous system that involves the difficulty or impossibility of understanding and formulating language. A typical disorder of non-fluent forms of aphasia is anomia. Anomia refers to the difficulty in finding words, in particular when trying to name objects and actions. According to the Embodied Cognition approach (EC), language is tightly connected to the motor system. In this view, language rehabilitation programs should stimulate language through the activation of the motor system. In this approach, since anomic deficits are often due to a weak link between the meaning of the word and its lemma, the Hebbs’ principles of coincident and correlated learning can be exploited, i.e., by intensifying the synchronous activation of lexicon and semantics and connecting them with the motor counterpart. In this study, the investigators present an innovative training, based on the EC framework, in which they will make use of new technologies for anomia rehabilitation in post-stroke patients. Specifically, the researchers will use immersive 360° videos representing everyday actions displayed from the first-person point of view, experienced through a head-mounted display. The training will be administered 3 times a week for 4 weeks. The control group will watch standard videos representing the same actions recorded from the third-person perspective. Naming abilities will be tested before and after the training together with other cognitive and psychological measures. The investigators expect that the group who will undergo the 360° video-based training will show greater improvement of performance compared to the control group.

    Inclusion Criteria:
  • naming disorder in the post-acute phase (index event occurring at least 6 months earlier)
  • to have already received rehabilitation treatment in the acute phase
  • noun naming below cut-off
  • verbs naming below cut- off
  • Exlcusion Criteria:
  • concomitant or pre-existing (with respect to the index event) neurological and psychiatric deficits
  • epilepsy
  • balance disorders
  • neglect

  • Contact Information:
    Alice Cancer, PhD
    Phone: +39 3488122121
    Email:
    Claudia Repetto, Prof
    Phone: +39 3488122121
    Email:
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    r-behroozmand@sc.edu

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    Dear Roozbeh Behroozmand,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Neural Bases of Vocal Sensorimotor Impairment in Aphasia

    Principle Investigator: Dr. Roozbeh Behroozmand
    Institution: The University of Texas at Dallas
    Country: United States
    City: Columbia, South Carolina

    Brief Description:
    Aphasia is the most common type of post-stroke communication disorder characterized by deficits in speech comprehension, production and control. While recovery can be promoted with speech therapy, improvement remains modest and typically requires a large number of sessions contributing to rising health care costs. Traditional aphasia therapy focus on enhancing speech motor output; however, recent evidence suggests that the auditory feedback also plays a critical role in fluent speech. Therefore, a key step toward refining treatment strategies is to develop objective biomarkers that can probe the integrity of sensorimotor mechanisms of speech auditory feedback and identify their impaired function in patients with post-stroke aphasia. This study aims to examine the behavioral, neurophysiological (EEG), and neuroimaging (fMRI) biomarkers of speech impairment following stroke with focus on understanding the role of auditory feedback for speech production and control. We plan to test individuals with post-stroke aphasia and a matched neuroptypical control group during different speech production tasks under the altered auditory feedback paradigm. In addition, we aim to examine the effect of audio-visual feedback training on enhancing communication ability during speech. These biomarkers will be combined with existing lesion-symptom-mapping data in the aphasic group in order to identify the patterns of brain damage and diminished structural connectivity within the auditory-motor areas of the left hemisphere that predict impaired sensorimotor processing of speech in aphasia. The long-term goal of this research is to develop a model for identifying the source of sensorimotor deficit and improve diagnosis and targeted treatment of speech disorders in aphasia.

    Inclusion Criteria:
  • A total of 50 individuals with aphasia due to chronic left hemisphere stroke (> 6 months post-stroke) and 50 age- and gender-matched healthy control subjects will be recruited in this study. The general inclusion criteria for all subjects include: age range 21-75 years, right-handed, and native speaker of English. The aphasic subjects have previously undergone neuro-psychological speech/language testing and have been diagnosed with one type of aphasia (e.g., Broca’s, Wernicke’s, conduction or anomic). Subjects in the control group will meet the inclusion criteria with having normal voice, speech, language, and hearing function and no history of neurological and psychiatric disorder. We expect that a significant proportion of aphasic patients will show symptoms associated with Apraxia of Speech (AOS) or dysarthria; however, these patients will not be excluded unless their deficits will preclude them from performing the experimental tasks.
  • Exlcusion Criteria:
  • Subjects with moderate to severe hearing, memory, and/or cognitive impairments will be excluded for both groups. In addition, subjects with history of peripheral laryngeal disorders (e.g., paresis or vocal fold paralysis) will be excluded. Subjects will undergo safety screening and will be excluded if there are any factors counter-indicative for EEG and/or MRI scanning.

  • Contact Information:
    Roozbeh Behroozmand, PhD
    Phone: 8037775055
    Email:
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    e.meier@northeastern.edu, s.intille@northeastern.edu

    Copy this email template into your email:

    Dear Erin L Meier and Stephen Intille,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Word Retrieval in the Wild in People With Post-Stroke Aphasia

    Principle Investigator: NA
    Institution: Northeastern University
    Country: United States
    City: Boston, Massachusetts

    Brief Description:
    People with post-stroke aphasia (PWA) suffer from anomia, a condition where they know what they want to say but cannot retrieve the words. For PWA, word retrieval changes moment-to-moment, leading to diminished motivation to participate in conversations and disengagement from social interactions. In the real world, anomia variability and severity are compounded by contextual factors of communication exchanges (noise, dual-tasking). Ecological momentary assessment (EMA) involves in-situ measurement of a behavior over time during everyday life. EMA has promise for capturing real-world anomia, yet EMA methods have not been tested in PWA. Therefore, the aims of this pilot study are to (1) determine the relative feasibility of two types of smartwatch-delivered EMA (traditional-EMA and micro-EMA) in PWA and (2) determine the extent to which patient-specific factors relate to feasibility. Twenty PWA will be recruited and randomly assigned to either traditional-EMA or micro-EMA conditions. To target in-situ anomia, PWA will complete 36 picture-naming trials/day for three weeks, delivered either as a single trial 36 times per day (micro-EMA) or in four sets of nine trials/set per day (traditional-EMA). Due to the “at-a-glance” single trial delivery of micro-EMA, the investigators hypothesize that PWA in the micro-EMA condition will demonstrate better protocol adherence than PWA in the traditional-EMA condition. Older age, more severe cognitive-linguistic deficits, and greater discomfort with technology will be related to poorer compliance, lower completion, greater perceived burden, and lower intelligibility of naming audio recordings. This bench-to-bedside research will begin a translational path to implement EMA/micro-EMA into routine assessment of aphasia.

    Inclusion Criteria:
  • Current/pre-stroke English proficiency,
  • Normal/corrected-to-normal vision and hearing,
  • Medical stability,
  • History of left hemisphere stroke at least six months prior to enrollment, and
  • Presence of aphasia
  • Exlcusion Criteria:
  • History of neurological disease affecting the brain other than stroke

  • Contact Information:
    Erin L Meier, PhD
    Phone: 617-373-7438
    Email:
    Stephen Intille, PhD
    Phone: 617-373-3711
    Email:
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    mary.sullivan@va.gov, alyssa.autenreith@va.gov

    Copy this email template into your email:

    Dear Mary Sullivan and Alyssa Autenreith,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Semantic Feature Analysis Treatment for Aphasia

    Principle Investigator: NA
    Institution: VA Pittsburgh Healthcare System
    Country: United States
    City: Pittsburgh, Pennsylvania

    Brief Description:
    This randomized controlled comparative effectiveness study examines manipulation of a key component of an established and efficacious treatment for naming impairments in aphasia, along with cognitive and brain correlates of treatment success. Study participants will be randomly assigned to one of two treatment conditions comparing two different versions of Semantic Feature Analysis treatment. Their performance on standardized and study-specific measures will be used to determine which version of the treatment provides superior outcomes, and measures of automatic language processing and functional brain imaging will also be used to identify the underlying neurocognitive mechanisms associated with positive treatment response.

    Inclusion Criteria:
  • 6 months post-onset of aphasia due to unilateral left-hemisphere (LH) stroke
  • Independent in activities of daily living (ADLs) necessary to live in community-based housing or available caregiver to assist with ADLs
  • Medically stable and able to tolerate intensive treatment schedule (e.g. no uncontrolled seizures, difficulty breathing, frequent migraines)
  • English as a first language
  • No participation in any other speech-language treatment during this study, including follow-up period
  • Sufficient auditory comprehension abilities demonstrated during screening
  • Sufficient naming impairment exhibited during screening
  • Exlcusion Criteria:
  • Right Hemisphere stroke
  • Neurological disease other than stroke
  • Significant psychiatric disorder
  • Severe motor speech disorder
  • Active substance dependence

  • Contact Information:
    Alyssa Autenreith, M.A.
    Phone: 412-360-6472
    Email:
    Mary Sullivan, B.S.
    Phone: 412-360-6495
    Email:
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    ruiqipanedu@163.com

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    Dear Ruiqi Pan,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    pBFS-guided Dual-target cTBS for Aphasia After Stroke

    Principle Investigator: NA
    Institution: Changping Laboratory
    Country: China
    City: Jinan, Shandong; Qingdao, Shandong

    Brief Description:
    The objective of this trial is to evaluate the effectiveness and safeness of personalized brain functional sectors (pBFS) technology-guided continuous theta burst stimulation (cTBS) on the inferior frontal gyrus (IFG) combined with the superior temporal gyrus (STG) for language function recovery in post-stroke aphasic patients.

    Inclusion Criteria:
  • The patient’s age ranges from 35 to 75 years old (including 35 and 75 years old);
  • Meet the diagnostic criteria for ischemic stroke (according to the guidelines developed by the American Heart Association/American Stroke Association in 2019 and the guidelines developed by the Neurology Branch of the Chinese Medical Association in 2018) or meet the diagnostic criteria for hemorrhagic stroke (according to the guidelines developed by the American Heart Association/American Stroke Association in 2022 and the guidelines developed by the Neurology Branch of the Chinese Medical Association in 2019) ,with lesions located in the left hemisphere, and a duration of illness ranging from 15 days to 6 months.
  • Diagnosed as aphasia patient according to the Chinese version of Western Aphasia Battery (WAB), with a WAB-aphasia quotient of less than 93.8 points;
  • First onset of stroke;
  • Normal language function before the onset of stroke, and the patient’s native language is Chinese with at least 6 years of education;
  • Understand the trial and signed the informed consent form.
  • Exlcusion Criteria:
  • Combined dysarthria (NIHSS item 10 score ≥2 points);
  • Aphasia caused by bilateral hemisphere stroke, brain tumor, traumatic brain injury, Parkinson’s disease, motor neuron disease, or other diseases;
  • Patients with implanted electronic devices such as cardiac pacemakers, cochlear implants, or other metal foreign bodies, or those with MRI contraindications such as claustrophobia or TMS treatment contraindications;
  • History of epilepsy;
  • Patient with concomitant severe systemic diseases affecting the heart, lungs, liver, kidneys, etc., and uncontrolled by conventional medication, as detected and confirmed through laboratory testing and examination;
  • Patients with consciousness disorders (NIHSS 1(a) score ≥1);
  • Patients with malignant hypertension;
  • Patients with severe organic diseases, such as malignant tumors, with an expected survival time of less than 1 year;
  • Patients with severe hearing, visual, cognitive impairment or inability to cooperate with the trial;
  • Patients with severe depression, anxiety, or diagnosed with other mental illnesses that prevent them from completing the trial;
  • Patients who have received other neuromodulation treatments such as TMS, transcranial electric stimulation, etc. in the 3 months prior to enrollment;
  • Patients with a history of alcoholism, drug abuse, or other substance abuse;
  • Patients with other abnormal findings that the researchers judge are not suitable for participation in this trial;
  • Patients who are unable to complete follow-up due to geographical or other reasons;
  • Women of childbearing age who are currently pregnant, breastfeeding, or planning or may become pregnant during the trial;
  • Patients who are currently participating in other clinical trials.

  • Contact Information:
    Ruiqi Pan
    Phone: 010-80726688
    Email:
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    Copy these email(s) into your email:

    jianting.huang@pku.edu.cn, ruiqipanedu@163.com

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    Dear Jianting Huang and Ruiqi Pan,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    pBFS-guided Multi-target cTBS for Aphasia After Stroke

    Principle Investigator: NA
    Institution: Changping Laboratory
    Country: China
    City: Baoding, Hebei; Chengde, Hebei; Shijiazhuang, Hebei

    Brief Description:
    In this study, a randomized, double-blind, parallel-controlled trial was employed to evaluate the effectiveness and safety of personalized brain functional sectors (pBFS) technology-guided continuous theta burst stimulation (cTBS) on the inferior frontal gyrus (IFG) combined with the superior temporal gyrus (STG) and the superior frontal gyrus (SFG) for language function recovery in post-stroke aphasic patients.

    Inclusion Criteria:
  • The patient’s age ranges from 35 to 75 years old (including 35 and 75 years old);
  • Meet the diagnostic criteria for ischemic stroke (according to the guidelines developed by the American Heart Association/American Stroke Association in 2019 and the guidelines developed by the Neurology Branch of the Chinese Medical Association in 2018) or meet the diagnostic criteria for hemorrhagic stroke (according to the guidelines developed by the American Heart Association/American Stroke Association in 2022 and the guidelines developed by the Neurology Branch of the Chinese Medical Association in 2019) ,with lesions located in the left hemisphere, and a duration of illness ranging from 15 days to 6 months.
  • Diagnosed as aphasia patient according to the Chinese version of Western Aphasia Battery (WAB), with a WAB-aphasia quotient of less than 93.8 points;
  • First onset of stroke;
  • Normal language function before the onset of stroke, and the patient’s native language is Chinese with at least 6 years of education;
  • Understand the trial and signed the informed consent form.
  • Exlcusion Criteria:
  • Combined dysarthria (NIHSS item 10 score ≥2 points);
  • Aphasia caused by bilateral hemisphere stroke, brain tumor, traumatic brain injury, Parkinson’s disease, motor neuron disease, or other diseases;
  • Patients with implanted electronic devices such as cardiac pacemakers, cochlear implants, or other metal foreign bodies, or those with MRI contraindications such as claustrophobia or TMS treatment contraindications;
  • History of epilepsy;
  • Patient with concomitant severe systemic diseases affecting the heart, lungs, liver, kidneys, etc., and uncontrolled by conventional medication, as detected and confirmed through laboratory testing and examination;
  • Patients with consciousness disorders (NIHSS 1(a) score ≥1);
  • Patients with malignant hypertension;
  • Patients with severe organic diseases, such as malignant tumors, with an expected survival time of less than 1 year;
  • Patients with severe hearing, visual, cognitive impairment or inability to cooperate with the trial;
  • Patients with severe depression, anxiety, or diagnosed with other mental illnesses that prevent them from completing the trial;
  • Patients who have received other neuromodulation treatments such as TMS, transcranial electric stimulation, etc. in the 3 months prior to enrollment;
  • Patients with a history of alcoholism, drug abuse, or other substance abuse;
  • Patients with other abnormal findings that the researchers judge are not suitable for participation in this trial;
  • Patients who are unable to complete follow-up due to geographical or other reasons;
  • Women of childbearing age who are currently pregnant, breastfeeding, or planning or may become pregnant during the trial;
  • Patients who are currently participating in other clinical trials.

  • Contact Information:
    Jianting Huang, MD,PhD
    Phone: 010-80726688
    Email:
    Ruiqi Pan
    Phone: 010-80726688
    Email:
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    nmartin@temple.edu, reillyj@temple.edu

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    Dear Nadine Martin and Jamie Reilly,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Theory-Driven Treatment of Language and Cognitive Processes in Aphasia

    Principle Investigator: Nadine Martin
    Institution: Temple University
    Country: United States
    City: Philadelphia, Pennsylvania

    Brief Description:

    The aim of this research is to translate a theory of the cognitive relationship between verbal short–term memory (STM) and word processing impairments in aphasia to treatment approaches for language impairment in aphasia. It has been proposed that the co-occurrence of these impairments is due to a disruption of cognitive processes that support both abilities: maintenance of activated semantic and phonological representations of words, hereafter the ‘activation–maintenance hypothesis’.

    This hypothesis will be tested in the context of a treatment approach that aims to improve word processing and verbal STM abilities.

    Inclusion Criteria:
    Experimental participants
  • :
  • Aphasia
  • Single left hemisphere lesions
  • Right handed
  • At least six months post-stroke
  • Aged 21 to 80
  • High-school educated with English as their primary language
  • Passed an audiometric pure tone, air conduction screening at 25 dB HL at 1K, 2K and 4K Hz for at least one ear (with or without correction)
  • Demonstrate adequate vision with or without correction.
  • Will not exclude individuals with a mild apraxia of speech or mild dysarthria of speech.
  • Exlcusion Criteria:
  • History of mental illness
  • Alcohol/substance abuse
  • Pregnant
  • Unable to personally give informed consent
  • Control participants:
  • :
  • Aged 21 to 80
  • High school educated or above
  • Pass an audiometric pure tone, air conduction screening at 25 dB HL at 1K, 2K and 4K Hz for at least one ear.

  • Contact Information:
    Jamie Reilly, Ph.D.
    Phone: 2152041870
    Email:
    Nadine Martin, Ph.D.
    Phone: 215 204 3995
    Email:
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    samuel.cason@pennmedicine.upenn.edu, hbc@pennmedicine.upenn.edu

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    Dear Samuel Cason and Principal Investigator,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Transcranial Magnetic Stimulation and Constraint Induced Language Therapy for Chronic Aphasia

    Principle Investigator: H. Branch Coslett
    Institution: University of Pennsylvania
    Country: United States
    City: Philadelphia, Pennsylvania

    Brief Description:
    Transcranial Magnetic Stimulation (TMS) has been demonstrated to improve language function in subjects with chronic aphasia in a number of small studies, many of which did not include a control group. Although the treatment appears promising, data to date do not permit an adequate assessment of the utility of the technique. The investigators propose to study the effects of TMS combined with Constraint Induced Language Therapy (CILT) in 75 subjects with chronic aphasia. Subjects will be randomized in a 2:1 ratio to TMS with CILT or sham TMS with CILT. One Hz TMS at 90% motor threshold will be delivered to the right inferior frontal gyrus for 20 minutes in 10 sessions over 2 weeks; language therapy will be provided for one hour immediately after the conclusion of each session of TMS. Change from baseline in the Western Aphasia Battery Aphasia Quotient at 6 months after the end of TMS treatment will serve as the primary outcome measure. A secondary aim is to identify anatomic and behavioral predictors of response to treatment. Finally, a third aim is to identify the mechanism underlying the beneficial effect of the treatment using a variety of imaging techniques. Subjects who have no contraindication to the MRI will undergo fMRI imaging prior to and at 6 months after therapy. Using modern network analyses and robust machine learning techniques, the investigators will identify changes in the strengths of connections between nodes in the language network to address specific hypotheses regarding the effects of TMS and CILT on brain organization that are associated with beneficial response to treatment.

    Inclusion Criteria:
  • Clinical evidence and MRI or CT verification of a single left hemisphere stroke with moderate to severe aphasia.
  • Suffered their stroke at least 6 months prior to their testing
  • Must be able to understand the nature of the study, and give informed consent
  • Exlcusion Criteria:
  • Multiple strokes (excluding small lacunar strokes) as defined by brain imaging
  • History of substance abuse
  • Previous head trauma with loss of consciousness for more than 5 minutes
  • Psychiatric illness (We note that subjects will be assessed with the 15-item Geriatric Depression scale. Because depression is very difficult to evaluate in aphasic subjects, potential subjects will not be excluded on the basis of the depression score)
  • Chronic exposure to medications that might be expected to have lasting consequences for the central nervous system (e.g. haloperidol, dopaminergics)
  • History of or neuropsychological findings suggestive of dementia

  • Contact Information:
    Principal Investigator
    Phone: 215-573-4336
    Email:
    Samuel Cason, MA
    Phone: 215-349-8585
    Email:
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    njpaik@snu.ac.kr, bluebelll@naver.com

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    Dear Nam-Jong Paik and Ji-Young Lee,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Effects of rTMS Based on Hemodynamic Activity for Language Recovery in Early Poststroke Aphasia

    Principle Investigator: Nam-Jong Paik
    Institution: Seoul National University Bundang Hospital
    Country: Korea, Republic of
    City: Seongnam-si, Korea, Gyeonggi-do

    Brief Description:
    The aim of this study is to assess the safety and clinical efficacy of repetitive transcranial magnetic stimulation (rTMS) based on hemodynamic brain activity pattern with functional near infrared spectroscopy (fNIRS) in early poststroke nonfluent aphasia patients.

    Inclusion Criteria:
  • 18-80 yrs old
  • Right-handed
  • Radiologically confirmed left hemisphere stroke within 6 months
  • Fluent in Korean
  • First ever stroke
  • Non-fluent (motor-dominant) aphasia
  • Written informed consent
  • Exlcusion Criteria:
  • Previous medical histories of stroke, cerebral vascular operation,
  • Seizure
  • Patients with traumatic brain injury
  • Unable to perform the language task
  • Severe cognitive impairment (MMSE less than 16)
  • Skin lesion in the stimulation site of scalp
  • Metal implants in the body (cardiac pacemaker or aneurysm clip)
  • Pregnancy, breastfeeding

  • Contact Information:
    Ji-Young Lee, MD
    Phone: 82-031-787-7731
    Email:
    Nam-Jong Paik, MD, PhD
    Phone: 82-031-787-6883
    Email:
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    aidan.rogers@mountsinai.org, Courtney.McSweeney@mountsinai.org

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    Dear Aidan Rogers and Courtney McSweeney,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Neuro Device for Aphasia

    Principle Investigator: Miguel Escalon
    Institution: Icahn School of Medicine at Mount Sinai
    Country: United States
    City: New York, New York

    Brief Description:
    The aim of the trial is to determine whether 75Hz transcranial alternating current stimulation (tACS) synchronized with therapeutic linguistic tasks is an effective form of therapy for post-stroke aphasia.

    Inclusion Criteria:
    Individuals with aphasia (assessed using the Boston Diagnostic Aphasia Examination) who perform the Naming Task in the range of 10%-60% accuracy will be included in the study. The overall baseline score in the Naming Task will be estimated from the two baseline measurements.
  • diagnosis of aphasia: Broca’s or mixed (based on the assessment of a Speech Language Pathologist).
  • presence of a focus of injury in the left hemisphere (within one hemisphere only) as a result of the first ischemic or hemorrhagic stroke (based on CT/MRI examination);
  • chronic stage of the disease - time since the stroke occurred over 6 months.
  • ability to achieve an accuracy in the Naming Task of 10-60%.
  • 18-80 years
  • right-handedness before the stroke.
  • ability to give informed written consent.
  • fluency in English.
  • Exlcusion Criteria:
  • severe cognitive, auditory or visual impairment that would preclude cognitive and language testing - inability to follow a two-step command.
  • presence of metal implants in the skull.
  • presence of major untreated or unstable psychiatric disease.
  • history of epilepsy or seizures.
  • ongoing medication that increases the risk of epileptic seizures.
  • presence in the body of cardiac stimulators or pacemaker.
  • history of speech, language, hearing, or intellectual disability during childhood.
  • pregnancy (based on declarations)

  • Contact Information:
    Aidan Rogers
    Phone:
    1. 308-9450
    Email:
    Courtney McSweeney
    Phone:
    1. 308-9450
    Email:
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    Copy these email(s) into your email:

    jdrichardson@unm.edu, hhubbard@unm.edu

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    Dear Jessica Richardson and Honey Hubbard,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Targeted TDCS to Enhance Speech-Language Treatment Outcome in Persons With Chronic Post-Stroke Aphasia

    Principle Investigator: Jessica Richardson
    Institution: University of New Mexico
    Country: United States
    City: Albuquerque, New Mexico

    Brief Description:
    62 patients who are one year post stroke and have Aphasia as a result of that stroke will be recruited. Participants will have 4 assessment sessions and 15 treatment sessions. The TDCS will be to right Inferior Frontal Gyrus (IFG) (25 active, 25 sham) for 15 days. A combined semantic feature analysis/phonological components analysis treatment will be paired with the stimulation. Two assessment sessions will be pretreatment, 1 session immediately post-treatment, and 1 session at 3 months follow-up.

    Inclusion Criteria:
  • aged 25-85
  • must be greater than 1 year post-stroke
  • must have a diagnosis of aphasia based on impaired performance on the Western Aphasia Battery-Revised, Boston Naming Test, or during discourse production
  • must be left-hemisphere dominant as demonstrated by aphasia onset subsequent to left hemisphere damage
  • must be stimulable for naming
  • Exlcusion Criteria:
  • comorbid neurological disease.
  • damage to the anterior right hemisphere.
  • significant mood disorder.
  • substance/alcohol dependence or abuse within the past year
  • presence of any implanted electrical device or contraindications to tDCS or MRI
  • recent medical instability (within 4 weeks)
  • pregnancy

  • Contact Information:
    Honey Hubbard
    Phone: 505 277-1765
    Email:
    Jessica Richardson, Ph.D.
    Phone: 505-433-7766
    Email:
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    julio.hpavon@northwestern.edu, lkinsey@sralab.org

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    Dear Julio Hernandez Pavon and Laura Kinsey,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Studying Language With Brain Stimulation in Aphasia

    Principle Investigator: Julio C Hernandez Pavon
    Institution: Shirley Ryan AbilityLab
    Country: United States
    City: Chicago, Illinois

    Brief Description:
    The overall goal of this study is to evaluate whether stimulation of two brain areas alongside behavioral speech-language therapy increases connectivity to improve language functions in stroke-aphasia patients.

    Inclusion Criteria:
  • Diagnosis of non-fluent aphasia due to a single, left-hemisphere stroke
  • ≧ six months post-stroke onset
  • WAB-R Fluency, Grammatical Competence, and Paraphasias Score between 2-6
  • 18+ years of age
  • Premorbidly right-handed
  • English-speaking
  • Ability to participate in fMRI / TMS protocol
  • Exlcusion Criteria:
  • Cardiac pacemaker or pacemaker wires; neurostimulators; implanted pumps
  • Metal in the body (rods, plates, screws, shrapnel, dentures, IUD) or metallic particles in the eye
  • Surgical clips in the head or previous neurosurgery
  • Any magnetic particles in the body
  • Cochlear implants
  • Prosthetic heart valves
  • Epilepsy or any other type of seizure history
  • History of significant head trauma (i.e., extended loss of consciousness, neurological sequelae)
  • Significant other disease (heart disease, malignant tumors, mental disorders)
  • Significant claustrophobia
  • Ménière’s disease
  • Medications that increase risk of seizures, for instance antipsychotic and antidepressant medications acting primarily on the central nervous system, which lower the seizure threshold such as antipsychotic drugs (chlorpromazine, clozapine) or tricyclic antidepressants
  • Non-prescribed drug use, for instance recreational marijuana
  • Unable to refrain from using any alcohol and nicotine products for at least 24 hours before the study Visits.

  • Contact Information:
    Julio Hernandez Pavon, PhD
    Phone: 3122386820
    Email:
    Laura Kinsey, MS, CCC-SLP
    Phone: 3122385691
    Email:
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    aphasialab@osu.edu, harnish.18@osu.edu

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    Dear Victoria Diedrichs and Stacy M Harnish,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Genetic and Cognitive Predictors of Aphasia Treatment Response

    Principle Investigator: NA
    Institution: Ohio State University
    Country: United States
    City: Columbus, Ohio

    Brief Description:
    Aphasia, or language impairment after a stroke, affects approximately 2 million people in the United States, with an estimated 180,000 new cases each year. The medical community cannot predict how well someone with aphasia will respond to treatment, as some people with aphasia are poor responders to intervention even when participating in empirically supported treatments. There is a strong likelihood that genetics play a role in language recovery after stroke, but very little research has been dedicated to investigating this link. This study will investigate whether two genes and cognitive abilities, such as memory, predict responsiveness to aphasia therapy for word-retrieval difficulties.

    Inclusion Criteria:
  • At least six months post-onset of a single left-hemisphere stroke
  • Chronic aphasia
  • Anomia (word-retrieval deficits)
  • Native English Speaker.
  • Exlcusion Criteria:
  • Severe motor speech disorders
  • Severe auditory comprehension deficits
  • Severe depression.
  • Diffuse injury or disease of the brain
  • Uncorrected vision or hearing difficulties
  • Contraindications for MRI (e.g. cardiac pacemaker, ferrous metal implants, claustrophobia, pregnancy).

  • Contact Information:
    Stacy M Harnish, PhD
    Phone: 6142471982
    Email:
    Victoria Diedrichs, MA, CCC-SLP
    Phone: 6146881471
    Email:
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    blackett@musc.edu

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    Dear Principal Investigator,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Stepped Care for Aphasia

    Principle Investigator: Deena Blackett
    Institution: Medical University of South Carolina
    Country: United States
    City: Charleston, South Carolina

    Brief Description:
    This study is recruiting people who had a stroke at least 1 month ago and now have a language impairment called aphasia. Living with aphasia can have devastating effects on communication and quality of life, and it is not uncommon for survivors with aphasia to face psychological problems like depression and anxiety. Participants who are eligible for this study will undergo baseline testing, engage in a 5-week treatment focused on psychological well-being, undergo post-treatment testing, and then testing again 1-month later. Check-in phone calls will be conducted during the 1-month off period and participants will be interviewed about their experience at the end of the study as well. Compensation will be provided to participants with aphasia.

    Inclusion Criteria:
  • 18-81 years old
  • Native English speaker (English fluency by age 7)
  • Aphasia as a result of a left-hemisphere ischemic or hemorrhagic stroke (WAB-R Aphasia Quotient < 93.8)
  • At least 1-month post-stroke
  • Confirmation of left hemisphere stroke per medical records
  • Discharged from hospital
  • Participant is willing and able to consent for themselves.
  • Exlcusion Criteria:
  • Uncorrected hearing or visual impairment that prevents completion of experimental activities as determined by self-report
  • History of other neurological disorder or disease beside stroke (e.g., dementia, traumatic brain injury) as determined by self-report and/or medical records
  • Self-reported history of premorbid learning disability
  • Severe auditory comprehension deficits (as indicated by a score of more than two standard deviations below norms on the Auditory Verbal section of WAB-R)

  • Contact Information:
    Principal Investigator
    Phone: 513-325-6737
    Email:
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    Copy these email(s) into your email:

    ays41@pitt.edu

    Copy this email template into your email:

    Dear Aysha Salter-Volz,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Adaptive Trial Scheduling in Naming Treatment for Aphasia

    Principle Investigator: William Evans
    Institution: University of Pittsburgh
    Country: United States
    City: Pittsburgh, Pennsylvania

    Brief Description:

    Aphasia is a language disorder caused by stroke and other acquired brain injuries that affects over two million people in the United States and which interferes with life participation and quality of life. Anomia (i.e., word- finding difficulty) is a primary frustration for people with aphasia. Picture-based naming treatments for anomia are widely used in aphasia rehabilitation, but current treatment approaches do not address the long-term retention of naming abilities and do not focus on using these naming abilities in daily life. The current research aims to evaluate novel anomia treatment approaches to improve long-term retention and generalization to everyday life.

    This study is one of two that are part of a larger grant. This record is for sub-study 2, which will evaluate the benefits of adaptive trial spacing.

    Inclusion Criteria:
  • Existing diagnosis of chronic (>6 months) aphasia subsequent to left hemisphere stroke.
  • Impaired performance on 2/8 sections of the Comprehensive Aphasia Test.
  • Must have access to a high-speed internet connection and be able to participate in telehealth.
  • Exlcusion Criteria:
  • History of other acquired or progressive neurological disease.
  • Significant language comprehension impairments (per performance on the CAT - individuals will be excluded if their spoken language comprehension mean modality T- score on the CAT falls below 40).
  • Unmanaged drug / alcohol dependence.
  • Severe diagnosed mood or behavioral disorders that require specialize mental health interventions.

  • Contact Information:
    Aysha Salter-Volz, M.S.
    Phone: 412-383-6943
    Email:
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    Copy these email(s) into your email:

    lkinsey@sralab.org

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    Dear Laura Kinsey,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Modulating Intensity and Dosage of Aphasia Scripts

    Principle Investigator: Leora Cherney
    Institution: Shirley Ryan AbilityLab
    Country: United States
    City: Chicago, Illinois

    Brief Description:
    The purpose of this study is to evaluate how changing conditions of speech-language treatment (namely, amount of repetition and distribution of practice schedule) affects the language outcome of participants with aphasia following a stroke. Using a computer based speech and language therapy program, participants will practice conversational scripts that are either short or long. Participants will practice for either 2 weeks (5 days a week) or for 5 weeks (2 days a week).

    Inclusion Criteria:
  • Men or women with diagnosis of aphasia
  • Left-hemisphere stroke
  • Aphasia Quotient score between 40-80 on the Western Aphasia Battery-Revised
  • At least 6 months post stroke
  • Completed at least eighth grade education
  • Premorbidly literate in English
  • Visual acuity no worse than 20/100 corrected in the better eye
  • Auditory acuity no worse than 30 dB HL on pure tone testing, aided in better ear
  • Not receiving speech-language therapy at the time of study
  • Exlcusion Criteria:
  • Any other neurological condition (other than cerebral vascular disease) that could potentially affect cognition or speech, such as Parkinson’s Disease, Alzheimer’s Dementia, traumatic brain injury
  • Any significant psychiatric history prior to the stroke, such as severe major depression or psychotic disorder requiring hospitalization; subjects with mood disorders who are currently stable on treatment will be considered
  • Active substance abuse

  • Contact Information:
    Laura Kinsey, MS, CCC-SLP
    Phone: 312-238-6163
    Email:
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    wangkai1964@126.com, baiyunong1990@163.com

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    Dear Kai Wang and Tongjian Bai,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    High Definition Transcranial Alternating Current Stimulation (HD-tACS) for Post-stroke Aphasia

    Principle Investigator: WANG KAI
    Institution: Anhui Medical University
    Country: China
    City: Hefei

    Brief Description:
    To investigate the intervention effect of high definition transcranial alternating current stimulation(HD-tACS) in chronic post-stroke aphasia and its underlying neural mechanism by MRI.

    Inclusion Criteria:
  • aphasia diagnosed by the ABC.
  • 18-75 years old.
  • native Chinese speaker.
  • right-handed.
  • post onset of stroke ≥6months.
  • Exlcusion Criteria:
  • mental illness .
  • severe dysarthria.
  • a history of head injury or surgery.
  • alcohol or substance abuse.
  • cerebral tumor or abscess.

  • Contact Information:
    Kai Wang, PhD
    Phone: +86-0551-62923704
    Email:
    Tongjian Bai
    Phone: +8615256972606
    Email:
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    ays41@pitt.edu

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    Dear Aysha Salter-Volz,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Balancing Effortful and Errorless Learning in Naming Treatment for Aphasia

    Principle Investigator: William Evans
    Institution: University of Pittsburgh
    Country: United States
    City: Pittsburgh, Pennsylvania

    Brief Description:

    Aphasia is a language disorder caused by stroke and other acquired brain injuries that affects over two million people in the United States and which interferes with life participation and quality of life. Anomia (i.e., word- finding difficulty) is a primary frustration for people with aphasia. Picture-based naming treatments for anomia are widely used in aphasia rehabilitation, but current treatment approaches do not address the long-term retention of naming abilities and do not focus on using these naming abilities in daily life. The current research aims to evaluate novel anomia treatment approaches to improve long-term retention and generalization to everyday life.

    This study is one of two that are part of a larger grant. This record is for sub-study 1, which will adaptively balance effort and accuracy using speeded naming deadlines.

    Inclusion Criteria:
  • Existing diagnosis of chronic (>6 months) aphasia subsequent to left hemisphere stroke.
  • Impaired performance on 2/8 sections of the Comprehensive Aphasia Test.
  • Exlcusion Criteria:
  • History of other acquired or progressive neurological disease.
  • Significant language comprehension impairments (per performance on the CAT - individuals will be excluded if their spoken language comprehension mean modality T- score on the CAT falls below 40).
  • Unmanaged drug / alcohol dependence.
  • Severe diagnosed mood or behavioral disorders that require specialize mental health interventions.

  • Contact Information:
    Aysha Salter-Volz, M.S.
    Phone: 412-383-6943
    Email:
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    earil100@syr.edu

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    Dear Ellyn A Riley,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Improving Aphasia Using Electrical Brain Stimulation

    Principle Investigator: NA
    Institution: Syracuse University
    Country: United States
    City: Syracuse, New York

    Brief Description:
    Language and communication are essential for almost every aspect of human life, but for people who have aphasia, a language processing disorder that can occur after stroke or brain injury, even simple conversations can become a formidable challenge. Speech and language therapy can help people recover their language ability, but often requires months or even years of therapy before a person is able to overcome these challenges. This research will investigate non-invasive brain stimulation as a way to enhance the effects of speech and language therapy, which may ultimately lead to better and faster recovery from stroke and aphasia. The investigators hypothesize that participants with aphasia who receive speech and language therapy paired with active electrical brain stimulation will improve significantly more on a language comprehension task than those who receive speech and language therapy paired with sham stimulation.

    Inclusion Criteria:
  • 18 years or older.
  • No diagnosis of neurological disorder (other than stroke).
  • No diagnosis of psychiatric disorder.
  • No seizure within the past 6 months.
  • Not pregnant.
  • In chronic phase of recovery, defined as at least 6 months post-stroke.
  • Not undergoing speech and language therapy targeting auditory comprehension or attention for the duration of the study.
  • No metal implants in the head.
  • No unhealed skull fractures.
  • Onset of aphasia related to left hemisphere stroke.
  • Damaged brain tissue from stroke does not overlap with left hemisphere dorsolateral prefrontal cortex.
  • Mild to moderate aphasia.
  • Cognitive ability minimally within functional limits.
  • Able to pass vision and hearing screening (with use of corrective aids if needed; eyeglasses, hearing aids).
  • Willing to allow audio-recording of study sessions.
  • Exlcusion Criteria:
  • Younger than 18 years old.
  • Diagnosis or history of neurological disorder other than stroke.
  • Diagnosis or history of psychiatric disorder.
  • History of seizures within the past 6 months.
  • Pregnant.
  • <6 months post-stroke (however, if this is only exclusionary criterion met, participant can be re-evaluated at the 6-month mark if still interested in the study)
  • Currently undergoing speech and language therapy targeting auditory comprehension or attention.
  • Metal implants in the head.
  • Currently has a skull fracture.
  • Onset of aphasia related to etiology other than left hemisphere stroke.
  • Damaged brain tissue includes left hemisphere dorsolateral prefrontal cortex.
  • No aphasia or severe aphasia.
  • Cognitive ability below functional limits.
  • Unable to pass vision and/or hearing screening with use of corrective aids.
  • Unwilling to allow audio-recording of study sessions.

  • Contact Information:
    Ellyn A Riley, PHD
    Phone: 315-443-9621
    Email:
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    Elena.Zevgolatakou@mrc-cbu.cam.ac.uk, Ajay.Halai@mrc-cbu.cam.ac.uk

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    Dear Eleni Zevgolatakou and Ajay Halai,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Speeded Anomia Treatment in Chronic Post-stroke Aphasia

    Principle Investigator: Matthew A. Lambon Ralph
    Institution: University of Cambridge
    Country: United Kingdom
    City: Cambridge

    Brief Description:
    The main aim of the study is to investigate the effect of a novel, speeded anomia therapy (Conroy et al., 2018) in a large population of patients with chronic post-stroke aphasia. The treatment will be delivered via a web application (QuickWord).

    Inclusion Criteria:
  • Native English speakers
  • Age 18 years or above
  • Stroke (any type) greater than 12 months post onset
  • No history of neurological disorders / psychiatric disorders
  • Normal or corrected-to-normal hearing & vision
  • Able to give informed consent
  • Currently not receiving Speech & Language therapy
  • Minimal repetition skills (>40% on an immediate word repetition test)
  • Evidence of naming difficulties (<90% in Boston Naming Test - Goodglass et al., 1983)
  • Exlcusion Criteria:
  • Non-native English speakers
  • Less than 18 years old
  • Stroke less than 12 months post onset
  • History of neurological disorders / psychiatric disorders
  • Uncorrected hearing & vision
  • Unable to give informed consent
  • Currently receiving Speech & Language therapy
  • Insufficient repetition skills (<40% on an immediate word repetition test)
  • Good naming performance (>90% in Boston Naming Test - Goodglass et al., 1983)

  • Contact Information:
    Ajay Halai, PhD
    Phone: +447724386296
    Email:
    Eleni Zevgolatakou, MSc
    Phone: +447508764348
    Email:
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    lcherney@sralab.org, sameer.ashaie@northwestern.edu

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    Dear Leora Cherney and Sameer Ashaie,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Timing of Transcranial Direct Current Stimulation (tDCS) Combined With Speech and Language Therapy (SLT)

    Principle Investigator: Leora Cherney
    Institution: Shirley Ryan AbilityLab
    Country: United States
    City: Chicago, Illinois

    Brief Description:
    Aphasia is an acquired (typically left-hemisphere) multi-modality disturbance of language that impacts around 2 million people in the USA. Aphasia impacts language production and comprehension as well as reading and writing. The ramifications of aphasia extend beyond language impairment to negatively impacting a person’s social, vocational, and recreational activities. Currently, the most effective way to treat aphasia is with speech-language therapy (SLT). However, even if SLT is intensive, persons with aphasia are left with residual language delays. Recent research suggests that pairing SLT with transcranial direct current stimulation (tDCS) a non-invasive, safe, low-cost form of brain stimulation may aid language recovery in persons with aphasia. However, results from tDCS studies are inconclusive. The success of tDCS in combination with SLT could depend on the timing of tDCS since tDCS-induced effects depend on the neuronal state of the brain-networks at the time of the stimulation. In this study, the differential impact of tDCS before behavioral SLT (offline-before therapy), tDCS after SLT (offline-after therapy), and tDCS concurrently with SLT (online) on functional language recovery in persons with aphasia will be investigated. Sham tDCS (i.e., SLT alone) as a control group will also be included in the study. The investigators hypothesize that both offline and online tDCS will improve language functioning than sham tDCS.

    Inclusion Criteria:
  • Men or women with diagnosis of fluent or non-fluent aphasia subsequent to a left-hemisphere infarct(s) that is confirmed by a MRI or CT scan
  • Aphasia quotient on the WAB of 35-85
  • At least 6 months post onset of aphasia (this is beyond the stage of spontaneous recovery)
  • 18- 80 years of age
  • Premorbidly fluent in English
  • Premorbidly right-hand dominant per the Edinburg Handedness Inventory
  • Visual acuity of 20/40 corrected
  • Auditory acuity no worse than 30 dB HL on pure tone testing, aided in the better ear.
  • Education greater than 12th grade
  • Exlcusion Criteria:
  • Any other neurological condition (other than cerebral vascular disease) that could impact language and cognition such as Alzheimer’s disease, Parkinson’s disease, primary progressive aphasia, and traumatic brain injury
  • Active substance use
  • Individuals with epilepsy

  • Contact Information:
    Leora Cherney, PhD
    Phone: 312-238-1117
    Email:
    Sameer Ashaie, PhD
    Phone: 312-238-6163
    Email:
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    shauna.zodrow@jefferson.edu

    Copy this email template into your email:

    Dear Shauna Zodrow,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Speech Entrainment Treatment for People With Aphasia

    Principle Investigator: Marja-Liisa Mailend, PhD
    Institution: Albert Einstein Healthcare Network
    Country: United States
    City: Elkins Park, Pennsylvania

    Brief Description:
    The objective of this research is to experimentally delineate the direct effect of speech entrainment practice on independent speech production and identify practice conditions that enhance treatment benefits. The primary outcome measure (Correct Information Units per minute) tallies informativeness and efficiency of independent speech in treated stories.

    Inclusion Criteria:
  • Between 18-80 years at the time of enrollment
  • English as native language
  • greater than six months post onset
  • Diagnosis of aphasia based on Western Aphasia Battery - Revised (WAB-R)
  • Score of 7 or less on the Fluency subsection of the WAB-R
  • Demonstrate having the willingness and stamina to participate in the multiple-session protocol, either by traveling to the MRRI testing site or being tested at home
  • Exlcusion Criteria:
  • History of learning disabilities
  • History of other comorbid neurological impairments

  • Contact Information:
    Shauna Zodrow, BA
    Phone: 215-663-6107
    Email:
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    claudio.brozzoli@inserm.fr, mallory.augier@gmail.com

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    Dear Claudio BROZZOLI and Mallory AUGIER,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Links Between Motor Abilities and Language Ability Deficits in Patients With Post-stroke Aphasia

    Principle Investigator: NA
    Institution: Hospices Civils de Lyon
    Country: France
    City: Bron Cedex; Bron; Saint-Genis-Laval

    Brief Description:

    Aphasia is a language disorder that affects oral and written expression and/or comprehension. It’s one of the most disabling consequence of stroke. Nowadays, aphasia rehabilitation is supported by speech therapists and is based on oral and written language, comprehension and expression. However recent studies have shown links between language and motor function (especially tool use). Two domains that share neural substrates (Broca’s area, basal ganglia) and that can influence each other.

    The aim of this study is to show that a motor training with a tool (pliers) can improve short-term and long-term language abilities of aphasic patients who had a stroke at least 3 months ago.

    The investigators hypothesis is that there is a learning transfer between tool use and language abilities in aphasic patients with an inferior frontal gyrus (IFG) lesion caused by a stroke, thanks to their shared neural resources.

    Investigators aim to study long and short-time effects of this tool motor training with three experiments:

    E1 will study short-term effects by estimating pre-post effect of a motor training on language abilities. Investigators will experiment different effectors: tool, hand, none (control group); on patients and healthy volunteers. E2 will study long-term effects with multiple single-case experimental designs (SCED). Patients will undergo four weeks of on-off design. E3 will study long-term effects by estimating the efficiency of an experimental sensorimotor protocol of four weeks, comparing a group of patients with the experimental sensorimotor protocol to a control group of patients

    Inclusion Criteria:
  • For all participants:
  • Adult male or female aged 18 years and over
  • Right-handed
  • Having signed an informed and written consent
  • Affiliated to a social security scheme
  • Have French as their first language
  • For patients :
  • Left inferior frontal gyrus lesion following a stroke
  • Stroke more than 3 months old
  • Aphasia proven by a pathological score on the A-2 test of the Syntax Comprehension Battery (BCS)
  • Exlcusion Criteria:
  • For all participants:
  • Cognitive abilities that prevent completion of the study tasks (assessed with the MOntreal Cognitive Assesment (MOCA))
  • Language skills impaired by other disorders (for example neurodegenerative disease)
  • Cognitive impairing treatments (for example psychotropic drugs)
  • Neurovisual disorder (hemineglect, unilateral spatial neglect)
  • Impairment of both upper limb abilities that prevent motor training (pathological score in the Purdue Pegboard Test and/or Box and Block Test).
  • Recurrence of a stroke impacting the reorganisation of neural networks
  • Persons deprived of their liberty by a judicial or administrative decision Persons of legal age under a legal protection measure (guardianship, curatorship)
  • Pregnant women, women in labour or nursing mothers, confirmed by questioning the participant
  • Participation in another study at the same time as this one

  • Contact Information:
    Claudio BROZZOLI
    Phone: 04 72 95 34 10
    Email:
    Mallory AUGIER
    Phone: 04 72 95 34 10
    Email:
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    argye@jhmi.edu, md.stockbridge@jhmi.edu

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    Dear Argye Hillis-Trupe and Melissa D Stockbridge,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Escitalopram and Language Intervention for Subacute Aphasia

    Principle Investigator: NA
    Institution: Johns Hopkins University
    Country: United States
    City: Baltimore, Maryland; Charleston, South Carolina; Columbia, South Carolina

    Brief Description:
    In this project, the investigators will investigate the effects of a selective serotonin reuptake inhibitor (SSRI), escitalopram, on augmenting language therapy effectiveness, as measured by naming untrained pictures and describing pictures, in individuals with aphasia in the acute and subacute post stroke period (i.e., within three months post stroke).

    Inclusion Criteria:
  • Participants must have sustained an acute ischemic left hemisphere stroke.
  • Participants must be fluent speakers of English by self-report.
  • Participants must be capable of giving informed consent or indicating a legally authorized representative to provide informed consent.
  • Participants must be age 18 or older.
  • Participants must be within 5 days of onset of stroke.
  • Participants must be pre-morbidly right-handed by self-report.
  • Participants must have an aphasia diagnosis as confirmed by the Western Aphasia Battery-Revised (Aphasia Quotient < 93.8).
  • Exlcusion Criteria:
  • Previous neurological disease affecting the brain including previous symptomatic stroke
  • Diagnosis of schizophrenia, autism, or other psychiatric or neurological condition that affects naming/language
  • A history of additional risk factors for torsades de pointes (TdP; e.g., heart failure, hypokalemia, family history of Long QT Syndrome)
  • Current severe depression, defined as a score of > 15 on the Patient Health Questionnaire (PHQ-9)
  • Uncorrected visual loss or hearing loss by self-report
  • Use of any medication approved by the FDA for treatment of depression at the time of stroke onset
  • Concomitant use of any monoamine oxidase inhibitors (MAOIs) or pimozide, or other drugs that prolong the QT/QTc interval, triptans (and other 5-Hydroxytryptamine Receptor Agonists), or other contraindications to escitalopram that may be identified.
  • A QTc greater than 450 milliseconds on electrocardiogram or evidence of hyponatremia (Na < 130) at baseline
  • Pregnancy at the time of stroke or planning to become pregnant during the study term.

  • Contact Information:
    Argye Hillis-Trupe, MD
    Phone:
    1. 614-2381
    Email:
    Melissa D Stockbridge, PhD
    Phone:
    1. 614-2381
    Email:
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    sschoenrock@mcw.edu, sapillay@mcw.edu

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    Dear Sidney E Schoenrock and Sara Pillay,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    HD-tDCS for Phonological Impairment in Aphasia

    Principle Investigator: Sara Pillay
    Institution: Medical College of Wisconsin
    Country: United States
    City: Milwaukee, Wisconsin

    Brief Description:
    This study will investigate the effects of mild electrical stimulation in conjunction with speech therapy for people with post-stroke aphasia to enhance language recovery.

    Inclusion Criteria:
  • Patients must be 18 or older.
  • Patients may not be older than 85.
  • Patients must have a language deficit from left-sided focal neurologic damage (e.g. stroke, tumor).
  • Patients must be adults and have English-language fluency.
  • Patients must be eligible to undergo MRI.
  • Beyond meeting the inclusion criteria, no preference will be given on the basis of race, ethnicity or gender.
  • Exlcusion Criteria:
  • Advanced neurodegenerative disease (i.e. Stage 3 Alzheimer’s disease)
  • Neurologic disease (e.g. idiopathic epilepsy, seizure disorders that are not well managed, Parkinson’s disease, ALS),
  • Severe psychopathology (e.g. schizophrenia, bipolar disorder, acute major depressive episode)
  • Suspected or diagnosed uncorrectable hearing or vision difficulties, or developmental disabilities (i.e. intellectual disability or learning disability).
  • Contraindications to MRI such as claustrophobia, implanted electronic devices, MRI-incompatible metal in the body, extreme obesity, pregnancy, inability to lie flat, inability to see or hear stimulus materials.
  • Younger than 18 or older than 85.
  • < 6 months post tumor resection.

  • Contact Information:
    Sara Pillay, Ph.D
    Phone: 414-955-7579
    Email:
    Sidney E Schoenrock, MA
    Phone: 414-955-4482
    Email:
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    agnes.floeel@uni-greifswald.de, nina.unger@uni-greifswald.de

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    Dear Agnes Floeel and Nina Unger,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Transcranial Direct Current Stimulation to Enhance Training Effectiveness in Chronic Post-Stroke Aphasia

    Principle Investigator: NA
    Institution: University Medicine Greifswald
    Country: Germany
    City: Aachen; Allensbach; Bad Aibling; Bad Homburg; Bad Klosterlausnitz; Bad Sülze; Berlin; Gailingen; Greifswald; Greifswald; Göppingen; Heidelberg; Kempen; Leipzig; Lindlar; Marbach; Meerbusch; Vechta

    Brief Description:
    The aim of the study is to investigate whether intensive speech-language therapy (SLT) combined with anodal transcranial direct current stimulation (tDCS) leads to better communication performance than SLT combined with placebo stimulation (using sham-tDCS).

    Inclusion Criteria:
  • left-hemisphere cortical or subcortical stroke with first-ever aphasic symptoms
  • at least 6 months post-onset of stroke;
  • aphasia, as determined by the Aachen Aphasia Test (AAT);
  • 13 moderate-to-severe word finding difficulties (maximum of 75% correct items on a computerized naming task at baseline);
  • at least 1 correct reaction on the first part of the AAT subscale Token Test (ensuring basic comprehension skills);
  • at least 1 point on the communicative task of the AAT subscale Spontaneous Speech (ensuring basic communication abilities);
  • German as first language;
  • intact left-hemisphere “hand knob” without right prefrontal lesions for placement of tDCS electrodes, as confirmed by magnetic resonance imaging or computer tomography scans.
  • Exlcusion Criteria:
  • contraindications for tDCS (e.g., cardiac pacemaker, history of seizures, implanted metal inside the head);
  • more than one clinically apparent stroke with aphasic symptoms;
  • other severe neurological diseases (e.g., brain tumor, and subdural hematoma);
  • epilepsy with seizures during the last 12 months prior to study start and/or intake of sedating antiepileptic drugs (barbiturates and benzodiazepines),
  • history of severe alcohol or drug abuse;
  • current severe depression;
  • current psychosis or other relevant psychiatric condition;
  • very severe apraxia of speech, as revealed by Hierarchical Word Lists;
  • severe non-verbal cognitive deficits, as indicated by the Corsi Block-Tapping Task;
  • severe uncontrolled medical problems;
  • severely impaired vision or hearing that prevents patients from engaging in intensive SLT;
  • changes in centrally active drugs within 2 weeks prior to study inclusion.

  • Contact Information:
    Agnes Floeel, Prof.
    Phone: +49 3834 86 6815
    Email:
    Nina Unger
    Phone: +49 3834 86 6749
    Email:
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    lzipse@mghihp.edu

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    Dear Lauryn Zipse,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Investigating the Effects of Rhythm and Entrainment on Fluency in People With Aphasia

    Principle Investigator: Lauryn Zipse, Ph.D., CCC-SLP
    Institution: MGH Institute of Health Professions
    Country: United States
    City: Boston, Massachusetts

    Brief Description:
    Speaking in unison with another person is included as a part of many treatment approaches for aphasia. It is not well understood why and how this technique works. One goal of this study is to determine who benefits from speaking in unison, and what characteristics of speech are most helpful. Another goal is to investigate a possible mechanism for this benefit: why does speaking in unison help? A possible mechanism for this benefit is examined, by testing whether the degree of alignment of a person’s speech with that of another speaker can account for unison benefit.

    Inclusion Criteria:
  • Native-speaker fluency in American English (prior to stroke for people with aphasia)
  • Controls must report no history of speech, language, neurological disorders, or stroke
  • People with aphasia must be at least 6-months post-stroke, and aphasia must be due to stroke
  • Exlcusion Criteria:
  • Inadequate hearing ability to reliably complete task: fail hearing screen
  • Inadequate cognitive ability to understand and remember task: fail cognition screening (different measures for controls and people with aphasia)
  • Inadequate speech repetition ability to complete task, or to be considered a control: fail speech repetition screening (different thresholds for controls and people with aphasia)
  • Inadequate auditory comprehension ability to understand task: fail auditory comprehension screen (people with aphasia only)

  • Contact Information:
    Lauryn Zipse, PhD
    Phone: 6176433245
    Email:
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    ruiqipanedu@163.com

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    Dear Ruiqi Pan,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Individualized Precision rTMS for Language Recovery in Patients After Ischemic Stroke: a Multi-center RCT

    Principle Investigator: NA
    Institution: Changping Laboratory
    Country: China
    City: Beijing

    Brief Description:
    The current multi-center study aims to evaluate the efficacy and safety of pBFS-guided rTMS Neuromodulation Treatment for the rehabilitation of language functions in ischemic stroke aphasic patients.

    Inclusion Criteria:
  • Patients between the ages of 35 and 75 years (including 35 and 75 years).
  • Meet the diagnostic criteria of acute ischemic stroke (using the 2019 American Heart Association/American Stroke Association Guidelines for the Early Management of Patients With Acute Ischemic Stroke: 2019 Update to the 2018 Guidelines for the Early Management of Acute Ischemic Stroke and the 2018 Chinese Society of Neurology Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke in China). All lesions should be in the left hemisphere, and the course of disease should be more than or equal to 2 months and less than or equal to 1 year .
  • Meet the diagnostic criteria for aphasia according to the Chinese version of the Western Aphasia Battery (WAB), with a WAB-aphasia quotient less than 93.8.
  • First onset, or with a history of stroke without apparent sequelae ( scored≤1 on modified Rankin Scale score (mRS) before the current stroke).
  • Normal functioning language abilities before the stroke, with Mandarin as their native language and an educational level higher than primary school (more than 6 years’ education).
  • Understand the trial and be able to provide informed consent.
  • Exlcusion Criteria:
  • Patients with comorbid severe dysarthria (NIHSS item 10 dysarthria ≥ 2).
  • Aphasia caused by other diseases such as brain tumor, Parkinson’s syndrome, motor neuron disease, cerebral hemorrhage, traumatic brain injury, etc.
  • Patients with MRI scan and TMS treatment contraindications, such as claustrophobia, cardiac pacemaker, cochlear implant or other metallic foreign body and any electronic device implanted in the body.
  • History of epilepsy (having at least 2 uninduced seizures more than 24h apart, or a diagnosis of epilepsy syndrome, or having seizures within the past 12 months).
  • Patients with severe combined cardiac, pulmonary, hepatic, renal and other systemic diseases that cannot be controlled by conventional medication.
  • Patients with comorbid disorders of consciousness ( NIHSS 1(a)≥1).
  • Patients with combined malignant hypertension (sudden and significant increase in blood pressure, with increased systolic and diastolic blood pressure, often persisting above 200/130 mmHg)
  • Patients with co-malignant neoplasm.
  • Patients with a life expectancy of less than 1 year due to causes other than stroke.
  • Patients with combined deafness, visual impairment, or severe cognitive impairment to the extent that they are unable to cooperate with the test.
  • Patients with severe depression, anxiety, or diagnosed with other mental disorders to the extent that they are unable to cooperate with the trial.
  • History of TMS, transcranial electrical stimulation and other neuromodulation treatments in the past 3 months.
  • History of alcohol, drug, and/or other abuse.
  • Patients with other test abnormalities judged by the investigator to be unsuitable for the trial.
  • Women of childbearing age who are pregnant or preparing for pregnancy.
  • Patients who are participating in other clinical research trials.

  • Contact Information:
    Ruiqi Pan
    Phone: 010-80726688
    Email:
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    DRMoser@uams.edu, PSCarr@uams.edu

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    Dear Dana Moser and Portia Carr,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Treatment Outcomes With tDCS in Post-Stroke Aphasia

    Principle Investigator: NA
    Institution: University of Arkansas
    Country: United States
    City: Little Rock, Arkansas

    Brief Description:
    The purpose this study is to test the utility of pairing external neuromodulation with behavioral language treatment to boost therapy outcomes and to investigate the mechanisms associated with recovery. Because all PWA have word retrieval deficits, this project will test if greater language gains can be achieved by supplementing anomia intervention with excitatory brain stimulation to the left hemisphere and will evaluate associated functional brain changes to aid the optimization of neural reorganization to facilitate language processing.

    Inclusion Criteria:
  • Presence of post-stroke aphasia
  • Single left hemisphere stroke etiology
  • At least 6 months post-stroke
  • Age range between 18 and 80 years old
  • Speak English as a native language
  • Adequate hearing and vision to complete the tasks
  • Exlcusion Criteria:
  • Severe auditory comprehension deficits (determined by pretest) (i.e., global aphasia, Wernicke’s aphasia, transcortical sensory aphasia)
  • Inability to provide informed consent
  • Co-occurring history of neurological disease/disorder/injury (e.g., traumatic brain injury, right hemisphere stroke, dementia)
  • Co-occurring history of a major mental illness (e.g., schizophrenia, drug addiction, bipolar)
  • Clinical conditions contraindicated for MRI or tDCS (e.g., implanted electrical devices, claustrophobia, seizure disorder)
  • Positive pregnancy test (for females)

  • Contact Information:
    Dana Moser, PhD, CCC-SLP
    Phone: 501-569-8914
    Email:
    Portia Carr
    Phone: 501-569-3155
    Email:
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    sdrane@mcw.edu

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    Dear Samantha Drane,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Transcranial Alternating Current Stimulation (tACS) in Aphasia

    Principle Investigator: Priyanka Shah-Basak, PhD
    Institution: Medical College of Wisconsin
    Country: United States
    City: Milwaukee, Wisconsin

    Brief Description:
    This study will assess the effects of transcranial alternating current stimulation (tACS) on language recovery after stroke as well as healthy language functions.

    Inclusion Criteria:
  • Healthy Controls
  • 18 years of age or older
  • Fluent in English
  • No history of neurological or psychiatric disorders
  • Stroke Patients
  • Diagnosed with post-stroke aphasia by referring physician/neuropsychologist
  • Consent date >=1 months after stroke onset
  • Right-handed
  • Fluent in English
  • 18 years of age or older
  • Exlcusion Criteria:
  • Severe cognitive, auditory or visual impairments that would preclude cognitive and language testing
  • Presence of major untreated or unstable psychiatric disease
  • A chronic medical condition that is not treated or is unstable
  • The presence of cardiac stimulators or pacemakers
  • Any metal implants in the skull
  • Contraindications to MRI or tACS
  • History of seizures
  • History of dyslexia or other developmental learning disabilities

  • Contact Information:
    Samantha Drane, MS
    Phone: 414-955-5891
    Email:
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    marion.fossard@unine.ch, celia.ericson@unine.ch

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    Dear Marion Fossard and Célia Ericson,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Treatment of Grammatical Time Marking in Post-Stroke Aphasia

    Principle Investigator: Marion Fossard
    Institution: University of Neuchatel
    Country: Switzerland
    City: Neuchâtel

    Brief Description:

    The study aims to assess a individual or group therapy’s effectiveness in grammatical time marking. The main objective is to examine whether the therapy improves grammatical time marking of inflected verbs treated on the sessions. We also explore whether the observed progress can be transferred to untrained items, more ecological contexts and if is maintained two and four weeks after the end of treatment.

    This therapy will be administered to nine individuals with brain lesions after stroke. Five individuals will take part of the individual therapy and four individuals will take part of the group therapy (two individuals per group). The therapy will last one month, at the rate of three weekly sessions of approximately one hour.

    Inclusion Criteria:
  • Have had an imaging-objectified stroke in adulthood that resulted in aphasia (fluent or non-fluent). The time between the stroke and participation in this study must be greater than 6 months.
  • Be a native French speaker or have excellent mastery of French.
  • Be between 18 and 75 years old.
  • Present grammatical tense marking disorders objectified by language evaluation (deficit scores on the “Batterie d’Évaluation de la Production Syntaxique” (BEPS) verb flexion task, Monetta et al., 2018; and/or on the “Test d’expression morpho-syntaxique fine” (T.E.M.F.) active sentence production subtask, Bernaert-Paul and Simonin, 2011).
  • Exlcusion Criteria:
  • Present chronic symptoms of a substance use disorder as defined by Diagnostic and Statistical Manual of Mental Disorders (DSM-V) criteria.
  • Have significant uncorrected vision and/or hearing impairment.
  • Have significant impairments in oral/written comprehension.
  • Present apraxia of speech or a severe arthritic disorder
  • Present hemineglect
  • Present impaired judgment and discernment, objectified by a neuropsychological evaluation

  • Contact Information:
    Célia Ericson
    Phone: +41 32 718 18 95
    Email:
    Marion Fossard
    Phone: +41 32 718 17 34
    Email:
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    claire.honeycutt@asu.edu

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    Dear Claire F Honeycutt,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Efficacy of START (Startle Rehabilitation Therapy) in the Treatment Stroke-induced Aphasia/Apraxia

    Principle Investigator: Claire Honeycutt
    Institution: Arizona State University
    Country: United States
    City: Tempe, Arizona

    Brief Description:
    A stratified, parallel-group, double-blind, randomized controlled trial of remotely delivered START treatment to individuals with severe-to-moderate stroke (with recruitment focused on individuals with low SES) will be conducted. Subjects and assessors will be blinded to the condition making the experiment double blind. Specifically, subjects will be told that we are exploring a new therapy that using different sounds to improve therapy. Parallel group design will ensure that subjects in the Control group are unaware that their “sounds” are softer than the START group. Trainers may become aware that a loud sound is present thus a unique Assessor will evaluate clinical performance before and after training making the study double-blind. Fifty-four subjects will undergo baseline testing in the laboratory to establish their capacity for functional and expressive speech as well as their self-reported health-related quality of life (power analysis below). Next, subjects will participate in a high-frequency, word-picture verification/ auditory-repetition treatment, 2 hr/day for 5 consecutive days focusing on expression of words of functional significance (e.g., water, fall). Subjects will either receive training with START or without (Control). Subjects will be re-tested immediately following training as well as one-month post to assess retention. Aim 1 will evaluate capacity of START to enhance SLT outcomes by assessing the % change in clinical assessment of functional and expressive speech. Our preliminary data points to a robust response [details]. Aim 2 will focus on the capacity of these changes to 1) be retained and 2) impact subject’s reported quality of life. NOTE: While we are planning in-person baseline, end, and retention testing, in response to COVID, we have established remote clinical screening using peer-reviewed validated techniques for WAB and ABA-2 (see Alternative Solutions). All preliminary data collected for this proposal were collected remotely via no-contact protocols.

    Inclusion Criteria:
  • 18 years old
  • Native English Speakers
  • Capacity to provide informed consent
  • Right-handed
  • Corrected to normal vision
  • Left hemisphere cerebral stroke at least 6 months prior to testing
  • Presence of severe-to-moderate, non-fluent aphasia, i.e. Aphasia Quotients of 0-50 on the Western Aphasia Battery-Revised (PsychCorp, 2007)
  • Corrected pure tone threshold (octave frequencies 250- 4000 Hz) norms for their age and gender41,42 NOTE: Audiometry data will be collected for all participants by lab personnel trained by an audiologist in a sound-attenuated booth. Based on our ongoing aphasia studies, we expect that ~30% of participants will use hearing aids; we will not exclude these individuals but rather include hearing aid use as a covariate in analyses.
  • Exlcusion Criteria:
  • Severe concurrent uncontrolled medical problems (e.g. cardiorespiratory impairment).

  • Contact Information:
    Claire F Honeycutt, PhD
    Phone: 4809658453
    Email:
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    min.wong@polyu.edu.hk, faisal.n.baig@polyu.edu.hk

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    Dear Min Ney WONG and Faisal N Baig,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    tDCS Effects on Brain Plasticity in Aphasia Treatment

    Principle Investigator: Dr Min Wong
    Institution: The Hong Kong Polytechnic University
    Country: Hong Kong
    City: Kowloon

    Brief Description:
    The efficacy of conventional speech therapy alone for aphasia recovery is inconclusive. The prospective study will monitor the effects of combined language therapy and tDCS through structural and functional MRI.

    Inclusion Criteria:
  • History of a single unilateral left-hemispheric stroke,
  • Right handedness
  • Demonstrated features of Broca’s Aphasia
  • Cantonese speaker
  • Comprehension sufficient to carry out tasks
  • No history of other neurological diseases
  • Exlcusion Criteria:
  • Aphasia due to reasons other than Stroke, Traumatic brain injury
  • Bilateral or multiple brain lesions
  • Wernicke’s aphasia and other speech disorders, degenerative, psychiatric or metabolic disorders
  • Deaf, blind, pregnant/ or preparing for pregnancy, cognitive issues, tattoos
  • Have cochlear implants, pacemaker, surgical nails for bone fracture, artificial joints, dental braces, dentures
  • Taking anti-depressant medications

  • Contact Information:
    Faisal N Baig, PhD
    Phone:
    1. 27667268
    Email:
    Min Ney WONG, PhD
    Phone:
    1. 27666561
    Email:
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    charlotta.saldert@neuro.gu.se, francesca.longoni@neuro.gu.se

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    Dear Charlotta Saldert and Francesca Longoni,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Effects of Verb Network Strengthening Treatment (VNeST) on Word Finding in Aphasia

    Principle Investigator: NA
    Institution: Göteborg University
    Country: Sweden
    City: Gothenburg, Västra Götaland

    Brief Description:
    Although there is evidence that speech-language therapy may improve speech in language disorders following left hemisphere stroke there is still a lack of evidence for which types of therapy are effective. Furthermore, in Sweden, as well as in several other countries, access to speech-language therapy is limited. The purpose of this clinical trial is to compare outcome from Verb Network Strengthening Treatment (VNeST) provided as In-Clinic therapy (I-CT) or as synchronous telepractice therapy (TP-T).

    Inclusion Criteria:
  • Aphasia and subjective experience of word finding difficulties
  • Diagnosed left-hemisphere stroke at least six months post-onset
  • With correction, sufficient hearing and vision to be able to participate in training and assessment
  • Primarily speaking Swedish for at least the last 15 years
  • Exlcusion Criteria:
  • Other neurological injury or disease
  • Moderately or severely impaired comprehension
  • Moderate-severe apraxia of speech or dysarthria which may interfere with assessment
  • Participation in any other speech-language treatment during the study
  • Active substance dependence

  • Contact Information:
    Charlotta Saldert, Prof
    Phone: +46317865662
    Email:
    Francesca Longoni, Dr
    Phone: +46317866886
    Email:
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    tmontagnon@chu-grenoble.fr

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    Dear University Hospital,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Sensory-Motor Integration for Speech Rehabilitation in Patients With Post-stroke Aphasia

    Principle Investigator: NA
    Institution: University Hospital, Grenoble
    Country: France
    City: Grenoble

    Brief Description:
    SEMO is a multidisciplinary project (language sciences, cognitive psychology and neuropsychology, physical medicine and rehabilitation, neurology, speech-language pathology, functional neuroimaging and engineering sciences) that aims first, to test and develop a novel speech rehabilitation program designed for patients with non-fluent aphasia and, second, to better describe neural reorganization after successful recovery. To this end, the investigators will conduct a prospective monocentric cross-over study, including two cohorts of post-stroke aphasic patients and two control groups.

    Inclusion Criteria:
  • patients with late sub-acute and chronic post-stroke (> 4 months) non-fluent aphasia after lesion in the dominant hemisphere for language
  • native speakers of French
  • normal or corrected to normal vision
  • satisfying all criteria for the MRI examination
  • Exlcusion Criteria:
  • patients with comprehension deficits, hemi-spatial neglect or upper limb apraxia

  • Contact Information:
    University Hospital, Grenoble
    Phone: 04 76 76 68 14
    Email:
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    sschoenrock@mcw.edu

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    Dear Sidney Schoenrock,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Effects of Transcranial Direct Current Stimulation (tDCS) on Language

    Principle Investigator: Sara Pillay
    Institution: Medical College of Wisconsin
    Country: United States
    City: Milwaukee, Wisconsin

    Brief Description:
    This study will investigate the effects of mild electrical stimulation in conjunction with speech therapy for people with post-stroke aphasia to enhance language recovery.

    Inclusion Criteria:
  • Patients with a language deficit from focal neurologic damage (e.g. stroke, tumor).
  • Patients must be adults and have English-language fluency.
  • Patients must be eligible to undergo MRI.
  • Exlcusion Criteria:
  • Advanced neurodegenerative disease (i.e. Stage 3 Alzheimer’s disease) or neurologic disorder (e.g. idiopathic epilepsy, Parkinson’s disease, ALS)
  • Severe psychopathology (e.g. schizophrenia, bipolar disorder, acute major depressive episode)
  • No suspected or diagnosed uncorrectable hearing or vision difficulties, or developmental disabilities (i.e. intellectual disability or learning disability).
  • Contraindications to MRI such as claustrophobia, implanted electronic devices, MRI-incompatible metal in the body, extreme obesity, pregnancy, inability to lie flat, and inability to see or hear stimulus materials

  • Contact Information:
    Sidney Schoenrock
    Phone: 414-955-7579
    Email:
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    amy.rodriguez@va.gov, Laura.Britan_Lang@va.gov

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    Dear Amy D Rodriguez and Laura Britan Lang,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Intention Treatment for Anomia

    Principle Investigator: NA
    Institution: VA Office of Research and Development
    Country: United States
    City: Decatur, Georgia

    Brief Description:
    Every year approximately 15,000 Veterans are hospitalized for stroke, and up to 40% of those Veterans will experience stroke-related language impairment (i.e., aphasia). Stroke-induced aphasia results in increased healthcare costs and decreased quality of life. As the population of Veterans continues to age, there will be an increasing number for Veterans living with the aphasia and its consequences. Those Veterans deserve to receive aphasia treatment designed to facilitate the best possible outcomes. In the proposed study, the investigators will investigate optimal treatment intensity and predictors of treatment response for a novel word retrieval treatment. The knowledge the investigators gain will have direct implications for the selecting the right treatment approach for the right Veteran.

    Inclusion Criteria:
  • English as primary language
  • > 6 months post-onset a left-hemisphere stroke. Multiple strokes are acceptable as long as they are confined to the left hemisphere.
  • Diagnosis of aphasia
  • Presence of word retrieval deficits
  • Adequate comprehension as judged by ability to complete two-step commands on the Western Aphasia Battery.
  • Exlcusion Criteria:
  • Severe apraxia of speech or dysarthria
  • Clinically significant depression
  • For MRI safety: implanted medical devices, metal in the body and claustrophobia.

  • Contact Information:
    Amy D Rodriguez, PhD
    Phone:
    1. 321-6111
    Email:
    Laura Britan Lang, MPH
    Phone:
    1. 321-6111
    Email:
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    joanne.loewy@mountsinai.org

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    Dear Joanne Loewy,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    The Impact of Group Singing on Patients With Stroke and Their Personal Caregivers

    Principle Investigator: Joanne Loewy
    Institution: Icahn School of Medicine at Mount Sinai
    Country: United States
    City: New York, New York

    Brief Description:
    The study will focus on the impact of communal singing on patients with stroke and their personal caregivers. Forty post-stroke patients will be randomly assigned to two groups: the first group of 20 stroke survivors and their caregivers (up to 40 total participants) will receive 6 months (approximately 24 sessions) of music therapy. The second control groups of 20 stroke survivors and their caregivers will receive standard post-stroke care

    Inclusion Criteria:
  • Stroke victim, regardless of level of stroke
  • Exlcusion Criteria:
  • None

  • Contact Information:
    Joanne Loewy, DA
    Phone: 212-420-3484
    Email:
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    sschoenrock@mcw.edu, prishah@mcw.edu

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    Dear Sidney E Schoenrock and Priyanka Shah-Basak,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Transcranial Alternating Current Stimulation (tACS) for the Recovery of Phonological Short-Term Memory in Patients With Aphasia After Stroke

    Principle Investigator: Priyanka Shah-Basak, PhD
    Institution: Medical College of Wisconsin
    Country: United States
    City: Milwaukee, Wisconsin

    Brief Description:
    This study will assess the effects of transcranial alternating current stimulation (tACS) on language recovery after stroke.

    Inclusion Criteria:
  • Diagnosed with left hemisphere stroke/aphasia
  • Consent date >= 1 month after stroke onset
  • Fluent in English
  • 18 years of age or older
  • Exlcusion Criteria:
  • Severe cognitive, auditory or visual impairments that would preclude cognitive and language testing
  • Presence of major untreated or unstable psychiatric disease
  • A chronic medical condition that is not treated or is unstable
  • The presence of cardiac stimulators or pacemakers
  • Contraindications to MRI or tACS, e.g. patients with metallic implants, and/or history of skull fractures, pregnancy, skin diseases
  • History of ongoing or unmanaged seizures
  • History of dyslexia or other developmental learning disabilities

  • Contact Information:
    Priyanka Shah-Basak, PhD
    Phone: 414-955-7579
    Email:
    Sidney E Schoenrock, MA
    Phone: 414-955-5752
    Email:
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    al1579@georgetown.edu, ehl4@georgetown.edu

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    Dear Alycia Laks and Elizabeth Lacey,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Brain-based Understanding of Individual Language Differences After Stroke

    Principle Investigator: NA
    Institution: Georgetown University
    Country: United States
    City: Washington, District of Columbia

    Brief Description:
    Strokes often cause a loss of communication ability, referred to as aphasia, as well as cognitive difficulties. Each stroke survivor has a unique pattern of strengths and weaknesses in communication and cognition, and a unique course of recovery. The BUILD study aims to understand the brain basis of these individual differences in stroke outcome. Participants with stroke as well as controls matched in age, educational background, race, and sex are examined using a combination of standardized and in-house tests of language and cognition to provide a detailed profile of strengths and weaknesses. Each participant will have between three and six sessions, including an MRI to measure details of the structure, function, and connections in the brain. The data are analyzed to test how patterns in the stroke lesion explain the patterns of communication and cognitive difficulties, and how patterns in the uninjured parts of the brain explain resilience and recovery from the stroke. Ultimately, we hope that BUILD will guide us toward new targets for brain stimulation treatments or other biologically based treatments that improve language and cognitive abilities after stroke.

    Inclusion Criteria:
  • Stroke Survivors:
  • Age >=18
  • Stroke in left hemisphere of brain with or without aphasia, or stroke elsewhere causing aphasia
  • Learned English at 8 years or younger
  • Controls:
  • Age >=18
  • No history of brain injury resulting from stroke, trauma, infection (i.e. encephalitis), or tumor
  • Learned English at 8 years or younger
  • Exlcusion Criteria:
  • History of other brain conditions that could impact interpretation of results (such as multiple sclerosis, premorbid dementia)
  • Severe psychiatric condition that would interfere with participation in the study
  • History of a learning disability that could impact interpretation of results
  • Additional

  • Contact Information:
    Alycia Laks, MS, CCC-SLP
    Phone: 202-687-5205
    Email:
    Elizabeth Lacey, PhD
    Phone: 202-270-6497
    Email:
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    argye@jhmi.edu, md.stockbridge@jhmi.edu

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    Dear Argye E Hillis and Melissa D Stockbridge,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Producing Increasingly Complex Themes Using Right-hemisphere Engagement (PICTURE) Implemented With Telemedicine

    Principle Investigator: NA
    Institution: Johns Hopkins University
    Country: United States
    City: Baltimore, Maryland

    Brief Description:
    The investigators propose a pilot crossover trial of 2 behavioral language treatments, with randomized order of treatments and blinded assessors, to determine if a therapy designed to stimulate right hemisphere functions (Producing Increasingly Complex Themes Using Right-hemisphere Engagement Implemented with Telemedicine - PICTURE IT; described below) is more effective in improving discourse than a published computer delivered lexical treatment (shown previously to improve naming) in subacute post-stroke aphasia.

    Inclusion Criteria:
  • Diagnosis of aphasia secondary to stroke and presence of naming deficits (at least 20% errors on the Boston Naming Test or Hopkins Action Naming Assessment)
  • Capable of giving informed consent or indicating another to provide informed consent
  • Age 18 or older
  • The stroke must have occurred between 1 month and 4 months prior to enrollment in the study or more than 6 months prior to enrollment in the study
  • Able to understand therapy tasks (as indicated by 5 probes of each)
  • Exlcusion Criteria:
  • Lack of English proficiency (by self/legally authorized representative report)
  • Prior history of neurologic disease affecting the brain (e.g., brain tumor, multiple sclerosis, traumatic brain injury) other than stroke
  • Prior history of severe psychiatric illness, developmental disorders or intellectual disability (e.g., PTSD, schizophrenia, obsessive-compulsive disorder, autism spectrum disorders)
  • Uncorrected severe visual loss or hearing loss by self-report and medical records

  • Contact Information:
    Argye E Hillis, MD
    Phone: 410-614-2381
    Email:
    Melissa D Stockbridge, PhD
    Phone: 410-614-2381
    Email:
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    Adrian.Guggisberg@insel.ch

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    Dear Adrian G Guggisberg,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Effects of Transcranial Direct Current Stimulation (tDCS) on Brain Organization and Naming in Aphasic Patients

    Principle Investigator: Adrian Guggisberg
    Institution: University Hospital, Geneva
    Country: Switzerland
    City: Geneva, GE

    Brief Description:

    High-Definition Transcranial Direct Current Stimulation (HD-tDCS) allows to induce, in a non-invasive way, a transient inhibitory or excitatory neuromodulation of a given cerebral region and to obtain a very focused cortical effect. Previous studies using HD-tDCS have shown the effectiveness of this stimulation technique for enhancing language recovery in patients with aphasia.

    However, language processes are not determined solely by local neural activity at a single site, but rather by the interaction between neural networks. This is because a large cortical network is involved in language processes and, therefore, the same language disorder may result from lesions at different locations in this network.

    The investigators hypothesize that anodal HD-tDCS will enhance neural interactions between language areas and, thereby, improve language processing and word learning.

    The investigators propose to carry out a study on chronic aphasic patients involving HD-tDCS of the Broca region (left inferior frontal gyrus) combined with a verb learning task.

    Inclusion Criteria:
  • Ischemic or hemorrhagic stroke
  • Presence of aphasia with difficulty finding words and/or naming objects/pictures
  • ≥12 months post-stroke
  • ≥ 18 years of age
  • French-speaking
  • Able to participate in 30-60 min therapeutic sessions (good concentration and understanding of the task and ability to follow instructions
  • Exlcusion Criteria:
  • Patients unable to understand the given information on the study and its objectives, or instructions for tasks performed.
  • Impaired alertness or delirium
  • Severe co-morbidity affecting speech
  • Contraindication to tDCS: pregnant women, patients with active implants such as pacemakers or cochlear implants, patients with one or more seizures, metal objects in the brain
  • Occurrence of a new stroke during the study protocol.

  • Contact Information:
    Adrian G Guggisberg, MD
    Phone: +41316323081
    Email:
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    gfz2102@cumc.columbia.edu, eg2972@cumc.columbia.edu

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    Dear Galen Ziaggi and Elena M. Golub,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Longitudinal Imaging of Microglial Activation in Different Clinical Variants of Alzheimer’s Disease

    Principle Investigator: James M Noble, MD, MS, CPH, FAAN
    Institution: Columbia University
    Country: United States
    City: New York, New York

    Brief Description:

    The purpose of this study is to determine how inflammation is related to other changes in the brain that occur during the progression of Alzheimer’s disease. The investigators are also studying how inflammation is related to the symptoms that first occur in patients with Alzheimer’s disease (AD). For this reason, the investigators are asking people with different versions of Alzheimer’s disease to participate. This includes patients with either:

    Posterior cortical atrophy - a version of Alzheimer’s disease with vision difficulties Logopenic variant primary progressive aphasia - a version of Alzheimer’s disease with language difficulties Amnestic Alzheimer’s disease - a “typical” version of Alzheimer’s disease with memory difficulties The investigators are also enrolling older adults with normal visual, language, and memory function.

    Inclusion Criteria:
  • Age 50 and over at time of screening.
  • At screening, must have no cognitive impairment, or meet criteria for amnestic Alzheimer’s disease, posterior cortical atrophy, or logopenic variant primary progressive aphasia. Diagnoses will be made based on history, exam, neuropsychological testing, brain MRI, and consensus diagnosis.
  • Patients must have Clinical Dementia Rating scale score of 0.5 or 1 at enrollment. Controls must have Clinical Dementia Rating scale score of 0 at enrollment.
  • Subjects unable to provide informed consent must have a surrogate decision maker.
  • Written and oral fluency in English.
  • Able to participate in all scheduled evaluations and to complete all required tests and procedures.
  • In the opinion of the PI, the subject must be considered likely to comply with the study protocol and to have a high probability of completing the study.
  • Exlcusion Criteria:
  • Past or present history of a brain disorder other than Alzheimer’s disease (including presence of cortical infarct on MRI even in absence of clinical stroke).
  • Serious medical conditions, which make study procedures of the current study unsafe. Such serious medical conditions include uncontrolled epilepsy and multiple serious injuries.
  • Contraindication to MRI scanning.
  • Conditions precluding entry into the scanners (e.g. morbid obesity, claustrophobia, etc.).
  • Exposure to research related radiation in the past year that, when combined with this study, would place subjects above the allowable limits.
  • Participation in the last year in a clinical trial for a disease modifying drug for AD.
  • Taking immunosuppressive medication (e.g., glucocorticoids, cytostatics, antibodies, drugs acting on immunophilins, interferons, tumor necrosis factor inhibitors). Nonsteroidal anti-inflammatory drugs (NSAIDs) are not exclusionary.

  • Contact Information:
    Elena M. Golub
    Phone: 212-305-9079
    Email:
    Galen Ziaggi
    Phone: 212-305-9079
    Email:
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    simona.spaccavento@icsmaugeri.it

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    Dear Simona Spaccavento,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Music Intervention and Transcranial Electrical Stimulation for Neurological Diseases

    Principle Investigator: Simona Spaccavento
    Institution: Istituti Clinici Scientifici Maugeri SpA
    Country: Italy
    City: Bari, Ba

    Brief Description:

    The goal of this clinical trial is to evaluate the efficacy of a musical interventionand non-invasive brain stimulation in neurological patients. The main questions it aims to answer are:

    to evaluate the residual neuroplastic processes in DOC state related to music exposure to determine the putative modulation of the aforementioned processes and the clinical outcome of DOC patients by non-pharmacological strategies, i.e., electric (tDCS) and music stimulation to evaluate the impact of this intervention on caregiver’s burden and psychological distress.

    Participants will be randomly assigned to one of three different music-listening intervention groups. Primary outcomes will be clinical, that is based on the neurologist’s observations of clinical improvement, and neurophysiological, collected pre-intervention, post-intervention and post-placebo.

    Inclusion Criteria:
  • Age > 18 years
  • Post-stroke aphasia
  • Post-stroke neglect
  • Patients with disorders of consciusness (DOC)
  • Exlcusion Criteria:
  • No auditory injury
  • no hystory of neurological disease
  • No hystory of psychiatric disease
  • Previous stroke
  • use of alcohol and drugs
  • premorbid dementia

  • Contact Information:
    Simona Spaccavento
    Phone: +393332783524
    Email:
    Help me write an email


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    aphasiaresearchlaboratory@gmail.com

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    Dear Swathi Kiran,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Functional reorganization of the language and domain-general multiple demand systems in aphasia

    Principle Investigator: Swathi Kiran
    Institution: Boston University
    Country: United States
    City: Boston, MA

    Contact Information:
    Swathi Kiran
    Phone: 617-353-2706
    Email:
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    This study was submitted manually, not through clinicaltrials.gov


    Copy these email(s) into your email:

    bcstark@iu.edu

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    Dear Brielle C. Stark,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Characterizing inner speech in aphasia

    Principle Investigator: Brielle C. Stark
    Institution: Indiana University Bloomington
    Country: United States
    City: Bloomington, IN

    Contact Information:
    Brielle C. Stark
    Phone: 770-548-7121
    Email:
    Help me write an email


    This study was submitted manually, not through clinicaltrials.gov


    Copy these email(s) into your email:

    bcstark@iu.edu

    Copy this email template into your email:

    Dear Brielle C. Stark,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Inner speech as a naming therapy predictor in aphasia

    Principle Investigator: Brielle C. Stark
    Institution: Indiana University Bloomington
    Country: United States
    City: Bloomington, IN

    Contact Information:
    Brielle C. Stark
    Phone: 770-548-7121
    Email:
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    This study was submitted manually, not through clinicaltrials.gov


    Copy these email(s) into your email:

    tbrancamp@med.unr.edu

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    Dear Tami Brancamp,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Measuring and understanding the experience of post-traumatic growth in aphasia

    Principle Investigator: Tami Brancamp
    Institution: University of Nevada Reno
    Country: United States
    City: Reno, NV

    Contact Information:
    Tami Brancamp
    Phone: 775-982-3300 ext:17141
    Email:
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    This study was submitted manually, not through clinicaltrials.gov


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    rharrington2@gsu.edu

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    Dear Rachael Harrington,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Reading in Aphasia

    Principle Investigator: Rachael Harrington
    Institution: Georgia State University
    Country: United States
    City: Atlanta, GA

    Contact Information:
    Rachael Harrington
    Phone: 404-413-6219
    Email:
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    This study was submitted manually, not through clinicaltrials.gov


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    aphasialab@pdx.edu

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    Dear Stacey Steel,

    I found your research on aphasiaresearch.org.
    I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
    The best way to contact me is:
      Caregiver: [Insert your phone / email]
      Person with aphasia: [Insert your phone / email]
    Thank you for doing this research.

    Sincerely,
    [Insert your name]

    Assessment of anomia: Improving efficiency and utility using item response theory

    Principle Investigator: Gerasimos Fergadiotis
    Institution: Portland State University
    Country: United States
    City: Portland, OR

    Contact Information:
    Stacey Steel
    Phone: 503-725-3275
    Email:
    Help me write an email


    This study was submitted manually, not through clinicaltrials.gov

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