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Behavior Therapy for Children and Adolescents With Obsessive-Compulsive Disorder (OCD)

This study has been completed.

Sponsored by: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)
ClinicalTrials.gov Identifier: NCT00000386
  Purpose

The purpose of this study is to evaluate a behavioral treatment program for children and adolescents with OCD and their families. Exposure and Response Prevention (ERP) behavior therapy, in which the patient is gradually exposed to the object or situation that causes anxiety and is taught to refrain from responding in a compulsive manner, is combined with family counseling (Family Treatment Program). This treatment will be compared to Relaxation Training (RT).

OCD is a long-term, often disabling disorder that can cause significant family disruption. ERP is a promising treatment for children with OCD, and it is thought that family participation (through the Family Treatment Program) may be a helpful addition. RT is a common treatment for anxiety.

Patients are assigned randomly (like tossing a coin) to receive either the ERP/Family Treatment Program or RT. Both treatments will be delivered over 12 90-minute outpatient sessions to youngsters and their families. All participants (patients and family members) will be assessed for treatment response each month during treatment, after treatment is finished, and then at 2 follow-up visits over the following 6 months.

A child/adolescent may be eligible for this study if he/she:

Has obsessive-compulsive disorder (OCD), is medication-free, and is 8 to 17 years old.


Condition Intervention Phase
Obsessive-Compulsive Disorder
Behavioral: Exposure and Response Prevention
Behavioral: Family Treatment Program
Behavioral: Relaxation Training
Behavioral: Behavior therapy
Behavioral: Family Counseling
Phase III

MedlinePlus related topics:   Anxiety    Obsessive-Compulsive Disorder   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized
Official Title:   Behavior Therapy for Childhood OCD

Further study details as provided by National Institute of Mental Health (NIMH):

Study Start Date:   December 1998
Estimated Study Completion Date:   November 2003

Detailed Description:

To evaluate a standardized multicomponent cognitive behavioral treatment program for child and adolescent obsessive-compulsive disorder (OCD). The treatment program consists of individual Exposure and Response Prevention (ERP) for the OCD child plus a concurrent family intervention designed to reduce OCD-related family conflict, facilitate family disengagement from the affected child's OCD behavior, and rebuild normal family interaction patterns. The ERP/Family Treatment Program is compared with Relaxation Training (RT).

OCD is a chronic, often disabling disorder in childhood that has been associated with increased rates of parental psychopathology and significant disruptions in family relationships and functioning. Preliminary studies suggest that ERP is an effective treatment for children with OCD although no controlled trials to this effect have been published. RT was selected as the comparison treatment because of its credibility as an anxiety treatment and familiarity to potential subjects. RT has been used as a comparison condition for at least 2 randomized controlled ERP trials for adult OCD and shown to be ineffective in treating this disorder. Although it has long been hypothesized that family participation in treatment may be helpful, this is the first controlled study incorporating a systematic manualized family treatment component.

Participants are randomly assigned to receive either the combined ERP/Family Treatment Program (n=56) or RT (n=24). Both treatments are delivered over 12 90-minute outpatient sessions according to detailed treatment manuals.Youth and families undergo comprehensive and systematic, including behavioral, assessments by blind clinical evaluators at baseline, monthly during treatment, post-treatment and 2 follow-up evaluations over 6 months. Treatment outcome is examined in multimodal fashion and across multiple functional domains with a special emphasis on family contextual variables. The impact of baseline functioning, including family context, and initial change over time on treatment outcome is also systematically evaluated.

  Eligibility
Ages Eligible for Study:   8 Years to 17 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

-

Patients must have:

Obsessive-compulsive disorder for which he/she has not received medication.

  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00000386

Locations
United States, California
Univ. of California / Los Angeles / Neuropsychiatric Inst.    
      Los Angeles, California, United States, 90024-1759

Sponsors and Collaborators

Investigators
Principal Investigator:     John C. Piacentini, PhD    
  More Information


Study ID Numbers:   R01 MH58459, DSIR CT-S
First Received:   November 2, 1999
Last Updated:   February 8, 2008
ClinicalTrials.gov Identifier:   NCT00000386
Health Authority:   United States: Federal Government

Keywords provided by National Institute of Mental Health (NIMH):
Adolescence  
Child  
Comparative Study  
Family  
Female  
Human
Male
Obsessive-Compulsive Disorder
Relaxation Techniques
Obsessive-Compulsive Disorder -- *therapy

Study placed in the following topic categories:
Anxiety Disorders
Mental Disorders
Obsessive-Compulsive Disorder

Additional relevant MeSH terms:
Pathologic Processes
Disease

ClinicalTrials.gov processed this record on December 03, 2008




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