Clinical Trial

Behavioral and Neural Correlates of Post-Stroke Fatigue

Active, Not Recruiting
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Summary
The goal of this phase I/II clinical trial is to determine the behavioral and neural effects of 5-daily transcranial direct current stimulation on post-stroke fatigue. The three aims are: Aim 1: Investigate the behavioral effect of 5 daily sessions of anodal tDCS over the ipsilesional M1 on PSF. Aim 2: Investigate the neurophysiological effect of 5 daily sessions of anodal tDCS over the ipsilesional M1. Aim 3: Determine the relationship between changes in M1 excitability, brain connectivity and changes in PSF. Participants will receive either a real or sham stimulation for 5 consecutive days and fatigue will be assessed before, immediately after and 1-month after the intervention. Fatigue will be assessed using clinical, behavioral, and neurophysiological outcomes.
Protocol Amendment History 2 changes
critical Enrollment closed, study ongoing 2026-08-08
minor Completion pushed: 2026-08-31 -> 2027-02-28 2026-08-08
Trial Details
NCT Number NCT06088914
Lead Sponsor Texas Woman's University
Collaborators: National Institutes of Health (NIH), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Conditions Stroke, Fatigue
Enrollment 32 participants
Start Date 2023-12-15
Primary Completion 2026-08-31 (estimated)
Study Completion 2027-02-28 (estimated)
Updated on ClinicalTrials.gov 2026-08-07