Actively Recruiting
tDCS for Post-Stroke Cognitive Impairment
Led by University of Oklahoma · Updated on 2024-10-10
80
Participants Needed
1
Research Sites
143 weeks
Total Duration
On this page
Sponsors
U
University of Oklahoma
Lead Sponsor
A
American Heart Association
Collaborating Sponsor
AI-Summary
What this Trial Is About
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).
CONDITIONS
Official Title
tDCS for Post-Stroke Cognitive Impairment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 to 99 years
- Ischemic stroke participants in sub-acute phase (at least 10 days after stroke or discharge and under 5 months post-event)
- Cognitive dysfunction with Montreal Cognitive Assessment (MoCA) score less than 26
You will not qualify if you...
- Clinically significant or unstable medical or psychiatric condition
- Diagnosis of severe depression
- History of relevant neurological diagnosis such as epilepsy
- Previous neurosurgical procedure with craniectomy
- Contraindications to tDCS such as implanted brain medical devices
- Severe visual impairment, hearing impairment, aphasia, neglect, or dementia
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Oklahoma
Oklahoma City, Oklahoma, United States, 73117
Actively Recruiting
Research Team
C
Cheryl Adams, RN
CONTACT
C
Camila Bonin Pinto, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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