Actively Recruiting
Collaborative Care in Posttraumatic Epilepsy
Led by Wake Forest University Health Sciences · Updated on 2026-02-03
40
Participants Needed
1
Research Sites
165 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this research is to evaluate a 6 month change in quality of life in subjects who receive collaborative care calls compared to those subjects who receive usual neurology care. This is a 2-site trial comparing a 24 week neurology-based collaborative care program to usual neurology care among a total of 60 adults with post-traumatic epilepsy.
CONDITIONS
Official Title
Collaborative Care in Posttraumatic Epilepsy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed and dated informed consent form provided
- Willingness to comply with all study procedures
- Diagnosis of post-traumatic epilepsy confirmed by neurologist impression or EEG findings
- History of at least mild traumatic brain injury verified by MIRECC screening or research database
- Traumatic brain injury occurred before epilepsy onset
- Symptoms of anxiety or depression as indicated by GAD-7 score of 8 or more, or NDDI-E score over 13
- Receiving clinical neurological care at one of the study sites
You will not qualify if you...
- Currently receiving psychiatric treatment judged to provide no added benefit from collaborative care
- Active suicidal ideation
- History of past suicide attempt
- Unstable drug or alcohol abuse
- Unstable or progressive medical conditions
- Participation in another treatment or intervention study
- Cognitive impairments preventing completion of anxiety and depression self-report assessments
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Atrium Health Wake Forest Baptist
Winston-Salem, North Carolina, United States, 27157
Actively Recruiting
Research Team
H
Heidi M. Munger Clary, MD, MPH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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