Anxiety and Depression in Epilepsy: A Pilot Treatment Study
Launched by WAKE FOREST UNIVERSITY HEALTH SCIENCES · May 1, 2018
Trial Information
Current as of June 07, 2025
Withdrawn
Keywords
ClinConnect Summary
This trial is an innovative learning healthcare system approach to translate the concept of measurement-based depression care into a specialty clinic setting and extend the concept to treat depression and/or anxiety. The neurologist/APP-administered medication intervention utilizes FDA-approved drugs with advantageous features for use in epilepsy (escitalopram and venlafaxine) and a telephone-based chronic care management plan for repeated symptom measurement and side effect surveillance. The proposed intervention may overcome barriers to implementing mental health treatment interventions i...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Provision of signed and dated informed consent form
- • Stated willingness to comply with all study procedures and availability for the duration of the study
- • Age 18 or older
- • Ability to take oral medication and the willing to adhere to the intervention regimen
- • Minimum of 1 prior clinic visit at the Comprehensive Epilepsy Center
- • Adequate cognition (MoCA score of 20 or greater)
- • Diagnosis of epilepsy: EEG with documented seizure or epileptiform discharges OR non-epileptiform EEG and seizure remission with antiseizure drug OR treating epileptologist's leading clinical impression is epilepsy
- • NDDI-E score greater than 15 and/or GAD-7 score greater than or equal to 10
- Exclusion Criteria:
- • Pregnancy or lactation
- • Known allergic reactions to escitalopram or venlafaxine
- • Comorbid psychogenic nonepileptic seizures
- • Prior psychiatric hospitalization
- • Prior suicide attempt
- • History of manic or psychotic symptoms (past manic episode (SCID-I), or psychotic symptom screen positive)
- • Current treatment by a psychiatrist or counselor/theraptist
- • Active suicidality at the time of screening
- • Current treatment with buspirone or an SSRI/SNRI/atypical antidepressant (specifically bupropion, fluoxetine, levomilnacipran, citalopram, milnacipran, desvenlafaxine, mirtazapine, duloxetine, paroxetine, escitalopram, sertraline, fluvoxamine, venlafaxine, vilazodone, vortioxetine)
About Wake Forest University Health Sciences
Wake Forest University Health Sciences is a leading academic research institution dedicated to advancing healthcare through innovative clinical trials and translational research. With a strong emphasis on multidisciplinary collaboration, the organization leverages its extensive expertise in medical research, patient care, and education to develop and evaluate new therapies and interventions. Committed to improving patient outcomes and public health, Wake Forest University Health Sciences fosters a dynamic environment for scientific inquiry, engaging in a wide range of clinical studies that address pressing health challenges. Through its rigorous methodologies and ethical standards, the institution aims to contribute significantly to the medical field and enhance the quality of life for diverse populations.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Winston Salem, North Carolina, United States
Patients applied
Trial Officials
Heidi Munger Clary, MD
Principal Investigator
Wake Forest University Health Sciences
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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