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Family Cognitive Behavioral Therapy for Obsessive-Compulsive Disorder

N/A
Recruiting
Led By S. Evelyn Stewart, MD
Research Sponsored by University of British Columbia
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Current DSM IV-TR Axis I diagnosis of childhood-onset OCD; Moderate to severe OCD (CY-BOCS≥16/40)
Male or female, aged 5-18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, midpoint, completion of 12 gf-cbt sessions, one-month follow-up
Awards & highlights

Study Summary

This trial will evaluate a type of therapy to treat OCD in children, testing its effects on OCD symptoms and functioning compared to a control group. #OCD #CBT #FamilyTherapy

Who is the study for?
This trial is for children and teens aged 5-18 with Obsessive-Compulsive Disorder (OCD). They must speak English, have a moderate to severe form of OCD, and be able to give informed consent along with their parents. Those with bipolar disorder, psychosis, mental retardation, autism spectrum disorders or substance abuse issues cannot participate.Check my eligibility
What is being tested?
The study tests Group-based Family Cognitive-Behavioral Therapy (GF-CBT) in treating pediatric OCD. Ninety participants will receive GF-CBT while another ninety on a waitlist serve as controls. The comparison focuses on changes in OCD severity and functioning after twelve GF-CBT sessions.See study design
What are the potential side effects?
Since the intervention involves therapy rather than medication, typical medical side effects are not expected. However, participants may experience emotional discomfort or increased anxiety when confronting fears during CBT.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I have been diagnosed with severe childhood-onset OCD.
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I am between 5 and 18 years old.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, midpoint, completion of 12 gf-cbt sessions, one-month follow-up
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, midpoint, completion of 12 gf-cbt sessions, one-month follow-up for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Children's Yale Brown Obsessive-Compulsive Scale (CY-BOCS)

Trial Design

2Treatment groups
Active Control
Group I: OCD-affected subjects (Group 1)Active Control1 Intervention
OCD-affected subjects will participate in 12 sessions of group therapy (as per GF-CBT protocol).
Group II: OCD-affected subjects (Group 2)Active Control1 Intervention
Waitlist affected-controls awaiting a treatment spot.

Find a Location

Who is running the clinical trial?

University of British ColumbiaLead Sponsor
1,415 Previous Clinical Trials
2,466,836 Total Patients Enrolled
6 Trials studying Obsessive-Compulsive Disorder
653 Patients Enrolled for Obsessive-Compulsive Disorder
Michael Smith Foundation for Health ResearchOTHER
19 Previous Clinical Trials
5,919 Total Patients Enrolled
2 Trials studying Obsessive-Compulsive Disorder
139 Patients Enrolled for Obsessive-Compulsive Disorder
S. Evelyn Stewart, MDPrincipal InvestigatorUniversity of British Columbia
3 Previous Clinical Trials
119 Total Patients Enrolled
3 Trials studying Obsessive-Compulsive Disorder
119 Patients Enrolled for Obsessive-Compulsive Disorder

Media Library

Group-based family cognitive-behavioural therapy Clinical Trial Eligibility Overview. Trial Name: NCT01635569 — N/A
Obsessive-Compulsive Disorder Research Study Groups: OCD-affected subjects (Group 1), OCD-affected subjects (Group 2)
Obsessive-Compulsive Disorder Clinical Trial 2023: Group-based family cognitive-behavioural therapy Highlights & Side Effects. Trial Name: NCT01635569 — N/A
Group-based family cognitive-behavioural therapy 2023 Treatment Timeline for Medical Study. Trial Name: NCT01635569 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~38 spots leftby Jun 2027