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:
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
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
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.
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.
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:
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.
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.
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.
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
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.
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.
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;
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
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)
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.
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.
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.
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
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
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:
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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.
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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
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
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.
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.
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
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.
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.
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.
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
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)
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.
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
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.
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).
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)
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.
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
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.
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.
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.
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)
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
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
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)
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
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.
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.
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.
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.
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
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)
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.
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)
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
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
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).
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
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
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
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.
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
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.
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
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
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
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
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.
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.
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
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.
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
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.
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
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I have aphasia and I'm interested in learning more about the study. I think I may meet the study criteria.
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Caregiver: [Insert your phone / email]
Person with aphasia: [Insert your phone / email]
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Measuring and understanding the experience of post-traumatic growth in aphasia
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.
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
This study was submitted manually, not through clinicaltrials.gov
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