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Family and Peer Involvement in the Treatment of Anxiety Disorders in Children - Article


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Child Behavior Disorders

Bullying


Clinical Trial: Family and Peer Involvement in the Treatment of Anxiety Disorders in Children

This study is currently recruiting patients.

Sponsored by: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)

Purpose

The purpose of this study is to compare the effectiveness of family- and peer-oriented therapy in treating children with anxiety disorders.

Condition Treatment or Intervention Phase
Anxiety Disorders
 Behavior: Cognitive Behavior Therapy
Phase I

MedlinePlus related topics:  Anxiety

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study

Official Title: Therapy Specificity and Mediation in Family and Group CBT

Further Study Details: 

Expected Total Enrollment:  250

Study start: July 2002;  Expected completion: June 2007

Data suggest that individual Cognitive Behavior Therapy (CBT) is effective in reducing anxiety disorders in children. The incorporation of family and peers in a CBT treatment program may be more effective in reducing anxiety symptoms than CBT alone because a child's environment affects the development, course, and outcome of childhood psychopathology and functional status. This study will evaluate the effectiveness of family and peer involvement in CBT treatment.

Children and their parents will be randomly assigned to one of two treatment conditions: Family/Parents CBT (FCBT) or Peer/Group CBT (GCBT) for 14 to 16 weekly sessions. Parent-child relationships are the focus of the FCBT. Parents will be trained to manage their children's anxiety and avoidant behaviors by increasing acceptance and warmth toward their children. Children in the GCBT group will be trained to be more helpful and positive toward other children through role-playing activities. Interviews, questionnaires, and behavior observation tasks will be used to assess participants. All participants will be assessed at pretreatment, post-treatment, and at yearly follow-up visits for 5 years.

Eligibility

Ages Eligible for Study:  8 Years   -   14 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion criteria:

  • DSM-IV criteria for Generalized Anxiety Disorder (GAD), Social Phobia (SP), or Separation Anxiety Disorder (SAD)
  • Mean score >= 4 on the Clinician's Rating Scale of Severity
  • Discontinuation of all other psychosocial treatment upon consultation with clinic staff and the service provider
  • Discontinuation of stimulants for Attention Deficit Hyperactivity Disorder (ADHD) or other psychopharmacological agents that would confound the study

Exclusion Criteria:

  • DSM-IV criteria for a disorder other than GAD, SP, and SAD
  • Diagnosis of any one of the following: pervasive developmental disorders, mental retardation, selective mutism, organic mental disorders, or schizophrenia and other psychotic disorders
  • At risk for harm to self or others

Location and Contact Information


Florida
      Florida International University, Miami,  Florida,  33174,  United States; Recruiting
Patricia R. Alvarez  305-348-2494    ALVAREZP@DSRT.FIU.EDU 
Wendy K. Silverman, PhD,  Principal Investigator
William Kurtines, PhD,  Sub-Investigator

More Information

Study ID Numbers:  63997-01A1
Record last reviewed:  October 2004
Last Updated:  October 13, 2004
Record first received:  December 2, 2003
ClinicalTrials.gov Identifier:  NCT00073645
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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Page Updated: September 6, 2005
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