Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT05609916
NA

CBT Augmentation to Promote Medication Discontinuation in Pediatric OCD

Sponsor: Baylor College of Medicine

View on ClinicalTrials.gov

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

Interventions

BEHAVIORAL

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