Actively Recruiting
Using Personalized Assessments in the Treatment of Childhood OCD
Led by Johns Hopkins University · Updated on 2026-05-11
30
Participants Needed
1
Research Sites
143 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
CONDITIONS
Official Title
Using Personalized Assessments in the Treatment of Childhood OCD
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be between 8 and 17 years of age
- Have a primary diagnosis of obsessive-compulsive disorder (OCD) confirmed by a structured clinical interview
- Have moderate OCD severity with a Children's Yale-Brown Obsessive-Compulsive Scale (CY-BOCS) total score of 16 or higher
- Be medication free or on a stable medication dose for at least 8 weeks before joining the study
- Be English speaking
You will not qualify if you...
- Have a psychotic disorder, bipolar disorder, or autism spectrum disorder
- Have significant suicidal thoughts requiring medical intervention
- Currently receiving psychotherapy for OCD
- Unable to complete study scales or attend study visits
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Johns Hopkins University School of Medicine
Baltimore, Maryland, United States, 21287
Actively Recruiting
Research Team
A
Alexandra Chang
CONTACT
L
Lauren Browning
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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