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Pervasive Developmental Disorders |
PDD; Pervasive Development Disorder |
Clinical Trial: Child and Adolescent Anxiety Disorders (CAMS)
This study is currently recruiting patients.
|
Purpose
The purpose of this study is to compare the effectiveness of interventions for children and adolescents with separation anxiety disorder, social phobia, and/or generalized anxiety disorder. This study will also determine how long the treatment effects last.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Anxiety Disorders | Drug: sertraline (Zoloft) Behavior: Cognitive Behavioral Therapy | Phase III |
MedlinePlus related topics: Anxiety
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study
Official Title: Child/Adolescent Anxiety Multimodal Treatment Study
Expected Total Enrollment: 318
Study start: January 2003; Expected completion: May 2007
Anxiety disorders are among the most common conditions affecting children and adolescents. These disorders impair school, social, and family functioning. When left untreated, they also put children at risk for major depression and substance abuse in late adolescence and adulthood. Effective treatments that alleviate symptoms and prevent long-term morbidity and mortality associated with childhood-onset anxiety disorders are needed.
During Phase I of this two-phase study, participants are randomly assigned to receive sertraline (Zoloft), cognitive behavioral therapy, a combination of these treatments, or a placebo for 12 weeks. Phase II involves a 6-month maintenance period for participants that respond to any of the three active treatments.
Eligibility
Ages Eligible for Study: 7 Years - 17 Years, Genders Eligible for Study: Both
Accepts Healthy Volunteers
Criteria
Inclusion Criteria:
- DSM-IV criteria for separation anxiety disorder, social phobia, or generalized anxiety disorder
Exclusion Criteria:
- Major neurological disorder or medical illness that would interfere with participation in the study
Location and Contact Information
Hyung Koo, R.N. 410-614-4001 hkoo@jhmi.edu
California
UCLA, Los Angeles, California, United States; Recruiting
John Piacentini, Ph.D., Principal Investigator
James McCracken, M.D., Principal Investigator
Lindsey Bergman, Ph.D., Sub-Investigator
Maryland
Johns Hopkins, Baltimore, Maryland, 21287, United States; Recruiting
Hyung Koo, R.N. 410-614-4001 hkoo@jhmi.edu
John T Walkup, M.D., Principal Investigator
Golda Ginsberg, Ph.D., Sub-Investigator
New York
New York University, New York, New York, United States; Recruiting
Anne Maria Albano, Ph.D., Principal Investigator
Glenn Hirsch, M.D., Principal Investigator
NYSPI/Columbia University, New York, New York, United States; Recruiting
Bruce Waslick, M.D., Principal Investigator
Michael Sweeney, Ph.D., Principal Investigator
North Carolina
Duke University, Durham, North Carolina, United States; Recruiting
John March, M.D., M.P.H., Principal Investigator
Scott Compton, Ph.D., Principal Investigator
Pennsylvania
Temple University/University of Pennsylvania, Philadelphia, Pennsylvania, United States; Recruiting
Alicia Webb, M.S. 215-204-7165 awebb002@astro.temple.edu
Philip Kendall, Ph.D., Principal Investigator
Moira Rynn, M.D., Principal Investigator
University of Pittsburgh/WPIC, Pittsburgh, Pennsylvania, United States; Recruiting
Boris Birmaher, M.D., Principal Investigator
David Brent, M.D., Principal Investigator
Satish Iyengar, Ph.D., Sub-Investigator
More Information
Record last reviewed: March 2004
Last Updated: October 13, 2004
Record first received: January 22, 2003
ClinicalTrials.gov Identifier: NCT00052078
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 8, 2005
Resources
- Pervasive Developmental Disorders (National Institute of Neurological Disorders and Stroke)

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