Using Personalized Assessments in the Treatment of Childhood OCD
ConditionObsessive-Compulsive Disorder
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age8-17
SponsorJohns Hopkins University
About this trial
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 criteria
Qualifiers
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;
Disqualifiers
the presence of psychotic disorder, bipolar disorder, or autism spectrum disorders;
significant suicidal ideation that warrants medical intervention;
concurrent psychotherapy for OCD;
inability to complete scales, or attend visits.
Trial design
Treatments tested in this trial
- Personalized Assessments
- Standard of Care
Treatment groups
30 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov