Depression, Epilepsy
Conditions
Keywords
depression, epilepsy, seizures
Brief summary
To define the benefits of antidepressant treatment or cognitive behavior therapy on mood, function, and quality of life in persons with depression and refractory epilepsy.
Detailed description
This randomized clinical trial will be conducted to compare the drug sertraline to cognitive behavioral therapy on symptoms of depression, antiepileptic medication compliance, seizure frequency, and quality of life outcomes in persons with depression and a seizure disorder or epilepsy. Approximately 140 persons will be enrolled in this study over a period of five years. Individual participation will last approximately 16 weeks. Study participants will be chosen randomly to receive either the study medication (sertraline) or cognitive behavior therapy for 16 weeks. Sertraline is approved by the Food and Drug Administration (FDA). Subjects who receive cognitive behavior therapy will be provided with a one-hour individual session with a licensed clinical psychologist each week for 15 weeks. All study participants will attend scheduled clinic visits every 4 weeks for 16 weeks.
Interventions
DRUGsertraline
Sertraline: 25-200mg PO (orally); Subjects begin at 25mg for week 1 and increase to 50mg at the beginning of week 2. Sertraline is increased in 50mg increments when subjects score in the depressed range on the CES-D, a questionnaire that is administered every 2 weeks over the 16 week intervention period. Subjects may reduce dosage if toxicity occurs.
BEHAVIORALcognitive behavior therapy
CBT (Cognitive Behavior Therapy) - CBT is a psychotherapy based on modifying cognitions, assumptions, beliefs and behaviors, with the aim of influencing disturbed emotions. Subjects will meet with a trained CBT therapist for 1 hour each week over the 16 week intervention period and will be given assignments to work on each week.
Sponsors
National Institute of Neurological Disorders and Stroke (NINDS)
Columbia University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
21 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
INCLUSION: * Must have a seizure disorder. * Must meet the DSM-IV criteria for major depression. * Must be willing to provide written informed consent. * Must be age 21 to 75 years old. * Must be compliant, cooperative, reliable, and able to follow instructions, and to visit the clinic on schedule. EXCLUSION: * Have active suicidal or homicidal ideation. * Have current alcohol or other substance abuse disorders or a history of bipolar depression or any psychotic disorder. * Are pregnant or lactating. * Are known to be hypersensitive to sertraline. * Have a progressive central nervous system disorder (such as a tumor or multiple sclerosis), or severe hepatic or renal disease (serum creatinine \>3 mg/dl). * Currently taking an antidepressant medication or seeing a therapist regularly.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| MINI | completed at screen and 16 weeks |
Secondary
| Measure | Time frame |
|---|---|
| Depression as measured by the CES-D | completed every 2 weeks during the 16 week intervention period and at 6 month and 1 year follow ups |
| Health Related Quality of life as measured by the QOILIE-89 | completed every 4 weeks during the 16 week intervention period and at 6 month and 1 year follow ups |
| antiepileptic medication compliance | assessed at 16 weeks |
| antiepileptic medication toxicity as measured by the AEP | assessed every 2 weeks during the 16 week intervention period |
| seizure frequency and seizure severity | assessed every 2 weeks during the 16 week intervention period |
Countries
United States
Outcome results
None listed