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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00690729
Other study ID # H06-170
Secondary ID
Status Completed
Phase N/A
First received June 3, 2008
Last updated August 26, 2010
Start date July 2005
Est. completion date August 2010

Study information

Verified date August 2010
Source University of Connecticut Health Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This 16-week program examines cognitive behavioral bibliotherapy to typical therapist-directed cognitive behavior therapy for children and adolescents with Obsessive Compulsive Disorder.


Description:

This study is designed to compare self-directed bibliotherapy and therapist-directed cognitive behavioral therapy for children and adolescents with Obsessive Compulsive Disorder (OCD). Both treatments involve exposure and response prevention (EX/RP), in which the child confronts OCD fears and is asked to refrain from compulsive rituals (such as repetitive handwashing, counting, etc.). Participants are requested to complete an initial evaluation to determine diagnosis, and four follow-up evaluations to assess symptom severity and change due to treatment for a total of 16 weeks. Participant involvement to self-directed bibliotherapy versus traditional cognitive-behavioral treatment will be determined through random assignment.

In the bibliotherapy condition, the child or adolescent will meet with a therapist twice over the course of treatment, along with a parent. The therapist will discuss a self-directed program of EX/RP to be implemented at a pace deemed appropriate by child and parent at their own home. The child and parent will be provided with a manual designed to instruct them how to cope with Obsessive Compulsive Disorder. This treatment involves the parent and child reading the book, performing exercises, and monitoring symptoms on a weekly basis for 8 weeks.

In the therapist-directed treatment condition, the child or adolescent will meet weekly with a therapist along with their parent. The therapist, parent, and child will work together to design and implement a program of EX/RP. This treatment involves performing exercises, monitoring symptoms on a weekly basis, and completing homework assignments. Parents will be asked to help coach their child with at-home exercises challenging the Obsessive Compulsive Disorder. This treatment lasts 12 weeks.

Evaluations will be conducted following the completion of each treatment to assess the efficacy of each treatment on OCD symptoms. The treatment and evaluations for OCD are provided free of charge.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date August 2010
Est. primary completion date March 2010
Accepts healthy volunteers No
Gender Both
Age group 8 Years to 18 Years
Eligibility Inclusion Criteria:

- Ages 8-18 years old

- Primary diagnosis of Obsessive Compulsive Disorder

- Both parent and child fluent in English

- Parents must read at least a 7th grade reading level

Exclusion Criteria:

- Primary psychiatric diagnosis other than OCD

- Current threat of harm to self or others

- New use or dosage change of OCD medication 60 days prior to starting program

- Current involvement with another psychosocial therapy

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Cognitive Behavioral Bibliotherapy
Minimal therapist direction for self-guided bibliotherapy involving exposure and response prevention
Cognitive Behavioral Therapy
Therapist-directed exposure and response prevention

Locations

Country Name City State
United States Institute of Living Hartford Connecticut
United States University of Connecticut Storrs Connecticut
United States University of Connecticut Waterbury Connecticut
United States University of Connecticut West Hartford Connecticut

Sponsors (1)

Lead Sponsor Collaborator
University of Connecticut Health Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Child Yale-Brown Obsessive Compulsive Scale 12 weeks No
Secondary NIMH Clinician's Global Impression weeks 4, 8, 12, 16 No
Secondary Children's Obsessional Compulsive Inventory weeks 4, 8, 12, and 16 No
Secondary Child OCD Impact Scale weeks 4, 8, 12, 16 No
Secondary March Anxiety Scale for Children weeks 4, 8, 12, 16 No
Secondary Children's Depression Inventory weeks 4, 8, 12, 16 No
Secondary Child Behavior Checklist weeks 4, 8, 12, 16 No
Secondary Family Assessment Measure III weeks 4, 8, 12, 16 No
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