Actively Recruiting
Targeting Neuroplasticity for Persistent Post-Concussive Cognitive Symptoms
Led by University of Minnesota · Updated on 2026-03-17
30
Participants Needed
1
Research Sites
95 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This project investigates an innovative combination of non-invasive neuromodulation (transcranial direct current stimulation - tDCS) and cognitive training as a novel treatment approach aimed at improving function in individuals suffering from persistent post-concussive syndrome (PPCS) following mild traumatic brain injury (mTBI).
CONDITIONS
Official Title
Targeting Neuroplasticity for Persistent Post-Concussive Cognitive Symptoms
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18-65
- Has sustained a single mild traumatic brain injury 3-12 months prior to enrollment
- Meets criteria for persistent post-concussive syndrome assessed using the CP Screen
- Has reliable access to a smartphone
You will not qualify if you...
- Unable to provide informed consent or complete study procedures
- History of moderate or severe traumatic brain injury
- Significant neurological or psychiatric disorders other than mild depression or anxiety related to PPCS
- Substance dependence within the last six months
- Contraindications to transcranial direct current stimulation such as implanted metal or scalp skin lesions
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Minnesota
Minneapolis, Minnesota, United States, 55455
Actively Recruiting
Research Team
M
Melanie Stimac
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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