Actively Recruiting
Collaborative Care to Improve Quality of Life for Anxiety and Depression in Epilepsy
Led by Wake Forest University Health Sciences · Updated on 2026-03-02
60
Participants Needed
1
Research Sites
23 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating a 24-week neurology-based collaborative care intervention compared to usual neurology care for adults with epilepsy who also experience anxiety or depression. This randomized trial aims to assess how this collaborative approach affects quality of life related to emotional health in people with epilepsy. The study is conducted by Wake Forest University Health Sciences and focuses on improving mental health management alongside neurological care. The collaborative care program involves a care manager or social worker and a psychiatrist who work together with the participant and their neurologist. Participants in the intervention group receive care management calls every two weeks to assess anxiety, depression, seizures, and side effects, along with brief therapy interventions. The team holds collaborative care conferences to create expert recommendations for managing anxiety and depression and communicate these between all providers. The control group receives ongoing usual neurology care without this additional collaborative support. Participants are involved for 24 weeks during which their emotional quality of life is measured using the Quality of Life in Epilepsy Inventory QOLIE-31. Other assessments include adherence to the intervention, changes in epilepsy-specific quality of life, depression symptoms using Becks Depression Inventory, and anxiety symptoms using the Epilepsy Anxiety Survey Instrument. The study tracks these outcomes at 6 months, with adherence evaluated at 12 weeks. Safety and effectiveness of the collaborative care approach are monitored throughout the trial duration.
CONDITIONS
Brief Title
Collaborative Care for Anxiety and Depression in Epilepsy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Provision of signed and dated Informed Consent Form
- Willingness to comply with all study procedures
- Males and Females aged 18 years or older
- Diagnosis of epilepsy based on neurology clinician impression or EEG findings
- Presence of anxiety or depression symptoms
- Receiving clinical neurological care at Atrium Health
You will not qualify if you...
- Current participation in another treatment or intervention study
- Cognitive limitations preventing completion of anxiety and depression self-report tools
- Medical condition with life expectancy less than 6 months
- Active ongoing psychiatric treatment by a psychiatrist
- Active suicidal ideation
- History of past suicide attempt with ongoing psychotherapy or psychiatric care in past year
- Recent suicide attempt with multiple psychotropic medications and judged unsuitable for collaborative care
- Unstable drug or alcohol abuse
Research Team
L
Lauren P Richmond
H
Heidi M Munger Clary, MD, MPH
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