RECRUITING

Using Personalized Assessments in the Treatment of Childhood OCD

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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

Official Title

Using Personalized Assessments in the Treatment of Childhood OCD

Quick Facts

Study Start:2024-04-03
Study Completion:2025-12-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06407648

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:8 Years to 17 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. 1. be 8-17 years of age;
  2. 2. meet diagnostic criteria for a primary diagnosis of OCD on a structured clinical interview;
  3. 3. have moderate OCD severity as evidenced by a CY-BOCS total score of ≥16;
  4. 4. medication free and/or on a stable dose of medication 8 weeks prior to study participation;
  5. 5. be English speaking.
  1. 1. the presence of psychotic disorder, bipolar disorder, or autism spectrum disorders;
  2. 2. significant suicidal ideation that warrants medical intervention;
  3. 3. concurrent psychotherapy for OCD;
  4. 4. inability to complete scales, or attend visits.

Contacts and Locations

Study Contact

Alexandra Chang
CONTACT
443-300-8836
coach@jhmi.edu
Lauren Browning
CONTACT
443-300-8836
coach@jhmi.edu

Principal Investigator

Joseph F. McGuire, PhD
PRINCIPAL_INVESTIGATOR
Johns Hopkins University

Study Locations (Sites)

Johns Hopkins University School of Medicine
Baltimore, Maryland, 21287
United States

Collaborators and Investigators

Sponsor: Johns Hopkins University

  • Joseph F. McGuire, PhD, PRINCIPAL_INVESTIGATOR, Johns Hopkins University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-04-03
Study Completion Date2025-12-30

Study Record Updates

Study Start Date2024-04-03
Study Completion Date2025-12-30

Terms related to this study

Keywords Provided by Researchers

  • children
  • adolescents
  • exposure with response prevention
  • cognitive behavioral therapy
  • ERP
  • CBT

Additional Relevant MeSH Terms

  • Obsessive-Compulsive Disorder