Evaluating Anodal tDCS Preceding Aphasia Therapy
- Conditions
- StrokeAphasia
- Interventions
- Device: transcranial direct current stimulation
- Registration Number
- NCT02249819
- Lead Sponsor
- Northwell Health
- Brief Summary
The purpose of this study is to determine if non-invasive brain stimulation (transcranial direct current stimulation) delivered prior to language therapy will improve word-finding in individuals with aphasia who are 6 months or greater post-stroke.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 15
- ≥ 18 years of age
- First single focal unilateral left hemisphere lesion with diagnosis verified by brain imaging (MRI or CT scans) that occurred at least 6 months prior
- Pre-morbidly right handed
- Pre-morbidly fluent English speaker
- Cognitive function sufficient to understand the experiments and follow instructions (per interview with Speech Pathologist)
- A baseline Aphasia Quotient score between 10 to 94 out of 100 points on the Western Aphasia Battery (neither completely without language comprehension/expression nor fully recovered from aphasia).
-
Ongoing use of CNS-active medications
-
Ongoing use of psychoactive medications, such as stimulants, antidepressants, and anti-psychotic medications
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Presence of additional potential tDCS risk factors:
- Damaged skin at the site of stimulation (i.e., skin with ingrown hairs, acne, razor nicks, wounds that have not healed, recent scar tissue, broken skin, etc.)
- Presence of an electrically, magnetically or mechanically activated implant (including cardiac pacemaker), an intracerebral vascular clip, or any other electrically sensitive support system
- Metal in any part of the body, including metal injury to the eye (jewelry must be removed during stimulation)
- A history of medication-resistant epilepsy in the family
- Past history of seizures or unexplained spells of loss of consciousness during the previous 36 months
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Pregnancy in women, as determined by self-report
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description anodal tDCS, then sham tDCS transcranial direct current stimulation Participants received 1 single 20 min session of anodal tDCS + computerized naming therapy. Following a 1 week washout period, they received 1 single 20 min session of sham tDCS + computerized aphasia therapy. Sequence of stimulation conditions was randomized across participants. sham tDCS, then anodal tDCS transcranial direct current stimulation Participants received 1 single 20 min session of sham tDCS + computerized naming therapy. Following a 1 week washout period, they received 1 single 20 min session of anodal tDCS + computerized aphasia therapy. Sequence of stimulation conditions was randomized across participants.
- Primary Outcome Measures
Name Time Method Mean Change in Picture-naming Accuracy Score baseline, discharge The mean change in verbal picture-naming accuracy score (out of 75) was calculated from baseline to discharge in each condition (sham and active tDCS).
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Feinstein Institute for Medical Research
🇺🇸Manhasset, New York, United States