Group Cognitive Behavioral Therapy to Treat Depression in an Epilepsy Clinic Setting
Recruitment status was Active, not recruiting
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This study involves a form of group therapy called Cognitive Behavioral Therapy or CBT for depressed patients with Epilepsy. The CBT groups will be tailored for an epilepsy clinic population. There are 12 sessions of therapy in the study held once a week for 12 weeks.
Condition | Intervention |
---|---|
Epilepsy Depressive Disorder |
Behavioral: Cognitive Behavioral Therapy (CBT) in a Group Format |
Study Type: | Interventional |
Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
- Beck Depression Inventory
- NDDI
Estimated Enrollment: | 60 |
Study Start Date: | August 2005 |
Estimated Study Completion Date: | January 2007 |
Depression is frequent in PWE and often missed for unclear reasons. Busy neurology clinics and their overworked physicians often lack psychiatric backup that may make inquiring about psychological issues problematic. In the psychiatric community, awareness of the need for depression intervention in the primary care clinic has been recognized for many years and several treatment models exist. This study will attempt to use one such model, i.e. Cognitive-Behavioral Therapy (CBT) using a group format and tailoring its use for an epilepsy clinic population.
Ages Eligible for Study: | 18 Years to 65 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria::- Patients will be screened with the Beck Depression Inventory. Those reaching the positive cut-off score of 11 (indicating at least a mild depression) will be entered into the study. Patients entered on antidepressants will be held at a stable dosage. Anti-epileptic drugs will also be maintained on the same dosage at entry into the study when possible clinically, after consultation with their neurologist. Exclusion Criteria:- Patients will be excluded if there is any active serious medical conditions, Standard Score<70 as assessed via the Wide Range Achievement Test, psychotic or substance abuse issues, those who are unable to maintain a stable dose of medications for the duration of study.
United States, California | |
Stanford University School of Medicine | |
Stanford, California, United States, 94305 |
Principal Investigator: | John J Barry | Stanford University |
No publications provided
ClinicalTrials.gov Identifier: | NCT00285740 History of Changes |
Other Study ID Numbers: | 2903, 34121 |
Study First Received: | January 31, 2006 |
Last Updated: | December 14, 2007 |
Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
Depressive Disorder Depression Epilepsy Mood Disorders Mental Disorders |
Behavioral Symptoms Brain Diseases Central Nervous System Diseases Nervous System Diseases |
ClinicalTrials.gov processed this record on October 16, 2012