Transcranial Direct Current Stimulation Investigations of Language Processing in Aphasia
Aphasia
About this trial
This is an interventional treatment trial for Aphasia focused on measuring stroke, non-invasive brain stimulation, transcranial direct current stimulation (tDCS)
Eligibility Criteria
Inclusion Criteria:
- 1. Presence of aphasia attributable to one or more unilateral left hemispheric stroke(s)
- 2. The most recent stroke must have occurred 6 months prior to inclusion in the study
- 3. Must speak English as a native language
- 4. Must be able to understand the nature of the study, and give informed consent
Exclusion Criteria:
- 1. Subjects with bilateral strokes.
- 2. History of neurologic illness(es) other than stroke
- 3. Current unstable medical illness(es)
- 4. Epilepsy or Seizure(s) within the last six months
- 5. Subjects with metallic objects in the face or head other than dental apparatus such as braces, fillings, and implants.
- 6. Subjects with Pacemakers or ICDs
- 7. Diagnosed psychiatric disorders
- 8. Pregnancy
- 9. Current alcohol or drug abuse
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
Sham Comparator
Site-Finding
Real tDCS
Sham tDCS
Each subject will receive anodal, cathodal, and sham stimulation to both the ipsilesional and contralesional hemispheres in a series of six sessions (one condition per session), each separated by at least two days. During anodal and cathodal tDCS sessions, subjects will receive stimulation for 20 minutes with a current of 2.0 mA using a 5x5 cm electrode. During sham tDCS, a 2.0 mA current will be delivered for approximately 30 seconds before being extinguished over a course of seconds. The participant will complete pre/post language testing at each session in order to determine if the subject is a tDCS responder and if so, which site produces the best transient language improvement in that individual. Subjects who do not respond to tDCS will not be invited to move forward to the treatment phase.
Half of our tDCS responders will be randomized to a group receiving 10 sessions (divided in to two five-day periods) of real tDCS. During real tDCS sessions, subjects will receive stimulation for 20 minutes at a current of 2.0 mA with a 5x5 cm electrode at their optimal responder site previously determined.
Half of our tDCS responders will be randomized to a group receiving 10 sessions (divided in to two five-day periods) of sham tDCS. During sham tDCS, a 2.0 mA current will be delivered for approximately 30 seconds at the beginning of the sham condition before being extinguished over the course of seconds. Individuals randomized into the sham arm will be offered the option to crossover to real tDCS after their participation is complete.