TTrialPathMatch Me to Trials
← Back to trials
RecruitingStrokeMild Cognitive Impairment

tDCS for Post-Stroke Cognitive Impairment

Eligible age

18–99 yrs

Accepts

All genders

Locations

1 state

Healthy volunteers

No

See if you qualify for this study

Answer a few quick questions about your location and health. Takes about a minute.

Check my eligibility →

About this study

This study will evaluate the effects of a form of non-invasive brain stimulation on brain functioning and memory in participants with post-stroke cognitive impairment (PSCI).

Sponsor: University of Oklahoma

You may qualify if…

  • ✓ 1\) ischemic stroke participants in sub-acute phase (at least 10 days after stroke event or discharge and under 5 months post-event) with cognitive dysfunction (MoCA \<26);

You may not qualify if…

  • ✕ 1. clinically significant or unstable medical or psychiatric condition;
  • ✕ 2. diagnosis of severe depression;
  • ✕ 3. history of relevant neurological diagnosis (e.g., epilepsy);
  • ✕ 4. previous neurosurgical procedure with craniectomy;
  • ✕ 5. contraindications to tDCS (implanted brain medical devices);
  • ✕ 6. severe visual impairment, hearing impairment, aphasia, neglect or dementia.

Where it's recruiting

Oklahoma

Oklahoma City

Source: ClinicalTrials.gov · NCT06516588 · last updated 2024-10-10

tDCS for Post-Stroke Cognitive Impairment · TrialPath