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Individual and Family Therapy for Children With Anxiety Disorders
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: NCT00081406
  Purpose

The purpose of this study is to compare three treatments to determine which is most effective in reducing anxiety in children.


Condition Intervention Phase
Anxiety
Behavioral: Individual Child CBT
Behavioral: Family CBT
Behavioral: Education/Support/Attention
Phase II
Phase III

MedlinePlus related topics: Anxiety
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Parallel Assignment, Efficacy Study
Official Title: Child and Family Therapy for Anxiety-Disordered Youth

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

Estimated Enrollment: 150
Study Start Date: July 2000
Detailed Description:

Children and their parents will complete a comprehensive diagnostic assessment to determine eligibility. The assessment will include an individual diagnostic interview with the child, interviews with the parents, and written observations of the child from family members and teachers. Participants will then be randomly assigned to receive individual cognitive behavioral therapy (ICBT), family CBT (FCBT), or education/support/attention (ESA) for 5 months. Children in the ICBT group will meet individually with a therapist. In the FCBT and ESA treatment groups, children and their parents will meet weekly with a therapist.

At the end of treatment and 1 year following treatment completion, families will complete another assessment to determine the effectiveness of each treatment at reducing short- and long-term anxiety symptoms in their children.

  Eligibility

Ages Eligible for Study:   9 Years to 13 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Child with DSM-IV criteria for separation anxiety disorder, social phobia, or generalized anxiety disorder

Exclusion Criteria for Child Participants:

  • IQ less than 80
  • Current use of anti-anxiety or antidepressant medications
  • Psychotic symptoms
  • Child and/or parent is non-English speaking
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00081406

Locations
United States, Pennsylvania
Temple University Child and Adolescent Anxiety Disorders Clinic
Philadelphia, Pennsylvania, United States, 19122
Sponsors and Collaborators
  More Information

Web site for Child and Adolescent Anxiety Disorders Clinic at Temple University  This link exits the ClinicalTrials.gov site

Publications:
Study ID Numbers: R01 MH59087, DSIR CT-S
Study First Received: April 9, 2004
Last Updated: November 18, 2005
ClinicalTrials.gov Identifier: NCT00081406  
Health Authority: United States: Federal Government

Study placed in the following topic categories:
Anxiety Disorders

ClinicalTrials.gov processed this record on January 16, 2009