Status:

RECRUITING

Brain Stimulation Effects on Post-Stroke Fatigue and Aphasia

Lead Sponsor:

Syracuse University

Collaborating Sponsors:

National Institute on Deafness and Other Communication Disorders (NIDCD)

Conditions:

Aphasia Following Cerebral Infarction

Stroke Ischemic

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The goal of this clinical trial is to determine if electrical brain stimulation applied to the front parts of the brain can help people who have had a stroke improve their fatigue, language, and atten...

Eligibility Criteria

Inclusion

  • 18 years or older.
  • No diagnosis of neurological disorder (other than stroke).
  • No diagnosis of psychiatric disorder, with the exception of anxiety and/or depression if it is managed through medication and/or behavioral intervention.
  • No seizure within the past 6 months.
  • Not pregnant.
  • Does not currently have cardiac pacemaker
  • In chronic phase of recovery, defined as at least 6 months post-stroke.
  • Not undergoing speech and language therapy targeting auditory comprehension or attention for the duration of the study.
  • No metal implants in the scalp or bone in the pre-frontal area of the head.
  • No unhealed skull fractures.
  • Onset of aphasia related to single, left hemisphere, ischemic stroke.
  • Damaged brain tissue from stroke does not overlap with left hemisphere dorsolateral prefrontal cortex.
  • Mild to moderate aphasia (as measured by WAB-R \*\*or QAB).
  • Self-report of post-stroke fatigue (as measured on SF-CAT)
  • No significant challenges with vision or hearing (with use of corrective aids if needed; eyeglasses, hearing aids).
  • Willing to allow audio-recording of study sessions.

Exclusion

  • Younger than 18 years old.
  • Diagnosis or history of neurological disorder other than stroke.
  • Diagnosis or history of psychiatric disorder with the exception of anxiety and/or depression if it is managed through medication and/or behavioral intervention.
  • History of seizures within the past 6 months.
  • Pregnant.
  • Currently has cardiac pacemaker
  • \<6 months post-stroke (however, if this is only exclusionary criterion met, participant can be re-evaluated at the 6-month mark if still interested in the study)
  • Currently undergoing speech and language therapy targeting auditory comprehension or attention.
  • Metal implants in the scalp or bone in the pre-frontal area of the head.
  • Currently has an unhealed skull fracture.
  • Onset of aphasia related to etiology other than ischemic left hemisphere stroke.
  • Damaged brain tissue significantly overlaps with left hemisphere dorsolateral prefrontal cortex.
  • No aphasia or severe aphasia (as measured by WAB-R \*\*or QAB).
  • Does not report experience of post-stroke fatigue (as measured on SF-CAT)
  • Significant challenges with vision and/or hearing (even with use of corrective aids).
  • Unwilling to allow audio-recording of study sessions.

Key Trial Info

Start Date :

August 4 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

November 1 2029

Estimated Enrollment :

60 Patients enrolled

Trial Details

Trial ID

NCT07151677

Start Date

August 4 2025

End Date

November 1 2029

Last Update

September 3 2025

Active Locations (2)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (2 locations)

1

University of Michigan

Ann Arbor, Michigan, United States, 48109

2

Syracuse University

Syracuse, New York, United States, 13244