Using Personalized Assessments in the Treatment of Childhood OCD

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The primary purpose of this study is to learn whether personalized assessment of obsessive-compulsive disorder (OCD) symptoms in childhood OCD using mobile health technology are feasible and acceptable for youth and parents. The investigators will also examine whether personalized cognitive-behavioral therapy (CBT) that is informed by personalized OCD assessments yields better clinical outcomes when compared to standard CBT for youth with OCD

Eligibility
Participation Requirements
Sex: All
Minimum Age: 8
Maximum Age: 17
Healthy Volunteers: f
View:

• be 8-17 years of age;

• meet diagnostic criteria for a primary diagnosis of OCD on a structured clinical interview;

• have moderate OCD severity as evidenced by a CY-BOCS total score of ≥16;

• medication free and/or on a stable dose of medication 8 weeks prior to study participation;

• be English speaking.

Locations
United States
Maryland
Johns Hopkins University School of Medicine
RECRUITING
Baltimore
Contact Information
Primary
Alexandra Chang
coach@jhmi.edu
443-300-8836
Backup
Lauren Browning
coach@jhmi.edu
443-300-8836
Time Frame
Start Date: 2024-04-03
Estimated Completion Date: 2026-12-30
Participants
Target number of participants: 30
Treatments
Experimental: Personalized Assessments
12 sessions of exposure with response prevention (ERP) that is guided by personalized assessments.
Active_comparator: Standard of Care
12 sessions of exposure with response prevention (ERP) that is guided using standard practice.
Related Therapeutic Areas
Sponsors
Leads: Johns Hopkins University

This content was sourced from clinicaltrials.gov