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Clinical Trial Summary

The investigators hypothesize that delivery of anodal tDCS to the left frontal head region will reduce fatigue severity following stroke.


Clinical Trial Description

The purpose of this study is to investigate transcranial direct current stimulation (tDCS) as a home-based non-pharmacologic intervention for post-stroke fatigue (PSF). Investigators will perform a double-blind, sham-controlled, randomized clinical trial with 24 subjects; 12 will receive sham stimulation and 12 will receive real stimulation. After a baseline assessment, the tDCS device will be applied for 20 minutes, once daily over the left dorsolateral prefrontal cortex (DLPFC), for a total of two weeks. Follow-up assessments with outcome metrics will be completed after the seventh and fourteenth sessions, and one-month following the start date (2 weeks post-treatment). In a randomly selected subset of both real and sham participants, rs-fMRI will be completed at baseline and post-treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05816603
Study type Interventional
Source Weill Medical College of Cornell University
Contact Raquel Queiruga, M.A.
Phone (212) 746-1509
Email rqu4002@med.cornell.edu
Status Recruiting
Phase Phase 2
Start date May 23, 2023
Completion date December 2025

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