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CBT Augmentation to Promote Medication Discontinuation in Pediatric OCD
Sponsor: Baylor College of Medicine
Summary
The purpose of this study is to examine whether youth with OCD who benefit from CBT augmentation to SRI can discontinue their medication without relapse over 24 weeks.
Key Details
Gender
All
Age Range
7 Years - 17 Years
Study Type
INTERVENTIONAL
Enrollment
200
Start Date
2022-11-30
Completion Date
2027-08-30
Last Updated
2025-07-20
Healthy Volunteers
No
Conditions
Interventions
Cognitive Behavioral Therapy
During Phase I, participants will receive open label (no blinding) CBT during their study participation for 12 to 18 weeks. During Phase II, participants will continue receiving CBT maintenance sessions every two weeks for the first 4 weeks, followed by sessions every four weeks. They will also meet with the study physician every 2 weeks via telepsychiatry appointments for clinical and scalar assessment.
Locations (1)
Baylor College of Medicine
Houston, Texas, United States