Stroke Clinical Trial
Official title:
Enhancing Aphasia Therapy With Anodal Transcranial Direct Current Stimulation in Chronic Stroke Patients
NCT number | NCT02461355 |
Other study ID # | AAAO1700 |
Secondary ID | |
Status | Terminated |
Phase | N/A |
First received | |
Last updated | |
Start date | June 2015 |
Est. completion date | June 2016 |
Verified date | April 2019 |
Source | Columbia University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a randomized, crossover design trial that will compare how anodal transcranial direct current stimulation (tDCS) versus sham tDCS administered during multiple sessions of scripting therapy affects the acquisition and retention of trained scripts.
Status | Terminated |
Enrollment | 2 |
Est. completion date | June 2016 |
Est. primary completion date | June 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 21 Years and older |
Eligibility |
Inclusion Criteria: 1. Age over 21 years 2. Ischemic left hemispheric stroke verified by imaging (CT or MRI) greater than 6 months ago 3. Residual non-fluent or anomic aphasia, with Western Aphasia Battery-Revised Aphasia Quotient score <60 4. Fluent English speaker prior to stroke 5. Right-handed prior to stroke 6. Ability to give informed consent and understand the tasks involved. Exclusion Criteria: 1. History of recurrent stroke, either ischemic or hemorrhagic, in the left middle cerebral artery territory 2. Imaging unavailable 3. Large middle cerebral artery infarct involving entire inferior division (temporo-parietal) territory 4. History of dementia prior to the stroke 5. History of seizure, prior electroconvulsive therapy, deep brain stimulators, or brain surgery 6. Social and/or personal circumstances that interfere with ability to return for therapy and assessment sessions. |
Country | Name | City | State |
---|---|---|---|
United States | Adler Aphasia Center | Maywood | New Jersey |
Lead Sponsor | Collaborator |
---|---|
Columbia University | Pitkin Foundation |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Change in Percent Script Words Omitted | Baseline to immediate, 2 weeks, and 4 weeks post-training | ||
Primary | Change in Percent Correct of Trained Scripts | From Baseline to up to 2 days post-training | ||
Primary | Change in Words Per Minute of Trained Scripts | From Baseline to up to 2 days post-training | ||
Secondary | Change in Percent Correct of Trained Scripts | Baseline to 2 weeks and 4 weeks post-training | ||
Secondary | Change in Words Per Minute of Trained Scripts | Baseline to 2 weeks and 4 weeks post-training |
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