Actively Recruiting
Stimulating After Recovery From Traumatic Brain Injury
Led by University of Minnesota · Updated on 2026-04-07
30
Participants Needed
1
Research Sites
145 weeks
Total Duration
On this page
Sponsors
U
University of Minnesota
Lead Sponsor
U
United States Department of Defense
Collaborating Sponsor
AI-Summary
What this Trial Is About
This is a preliminary, prospective interventional study to investigate the feasibility of using transcutaneous alternating current stimulation (TACS) after a traumatic brain injury (TBI) to improve cognitive function and decision-making.
CONDITIONS
Official Title
Stimulating After Recovery From Traumatic Brain Injury
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults 18 years and older
- Diagnosis of a mild to moderate TBI (GCS > 8 on admission)
- Able to perform a computerized assessment
- Willing to attend all scheduled appointments
- Able to undergo the informed consent process
- Healthy participants must be adults 18 years and older
- Healthy participants must be able to perform a computerized assessment
- Healthy participants must be willing to attend all scheduled appointments
- Healthy participants must be able to undergo the informed consent process
You will not qualify if you...
- Open wound on scalp
- Severe TBI diagnosis or GCS of less than 8 on admission
- Non-English speaking
- Incarcerated
- Implanted defibrillator or pacemaker
- Visual impairment that hinders ability to complete computerized assessments
- Healthy subjects under 18 years of age
- Healthy subjects with open wound on scalp
- Healthy subjects with TBI diagnosis
- Healthy subjects who are non-English speaking
- Healthy subjects who are incarcerated
- Healthy subjects with implanted defibrillator or pacemaker
- Healthy subjects with visual impairment that hinders ability to complete computerized assessments
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hennepin County Medical Center
Minneapolis, Minnesota, United States, 55415
Actively Recruiting
Research Team
D
David Darrow, MD
CONTACT
D
David Darrow, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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