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

ConditionsStrokeAphasia
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age25-85
SponsorUniversity of New Mexico

About this trial

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.

Eligibility criteria

Qualifiers

aged 25-85

must be greater than 6 months 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

Disqualifiers

comorbid neurological disease.

damage to the anterior right hemisphere.

significant mood disorder.

substance/alcohol dependence or abuse within the past year

Trial design

Treatments tested in this trial

  • Active Comparator: Experimental: Active cathodal tDCS + language training
  • Sham Comparator: Placebo cathodal tDCS + Speech and language

Treatment groups

50 Participants
are divided into 2 treatment groups

Sponsors and collaborators

University of New Mexico

Lead sponsor

National Institutes of Health (NIH)

Collaborator

National Institute of General Medical Sciences (NIGMS)

Collaborator

National Institute on Deafness and Other Communication Disorders (NIDCD)

Collaborator