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Clinical Trials/NCT00247754
NCT00247754
Completed
Not Applicable

VP3: Vancouver Primary Prevention Program (Anxiety Disorders Prevention in School Children)

University of British Columbia1 site in 1 country281 target enrollmentNovember 2002
ConditionsAnxiety

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anxiety
Sponsor
University of British Columbia
Enrollment
281
Locations
1
Primary Endpoint
Anxiety symptoms
Status
Completed
Last Updated
20 years ago

Overview

Brief Summary

Objective:

  1. To evaluate the efficacy of a school-based cognitive behavior therapy (CBT) program in reducing anxiety disorder symptoms in at-risk public school children.
  2. To determine whether parent education and involvement improves outcome in anxious children treated with CBT.
  3. To determine the ability of school personnel in a) recognizing classroom behaviors as anxiety disordered after targeting training of observable child behaviors e.g., avoidance, over-worry, etc.), and b) delivering a cognitive behavior intervention and
  4. To evaluate a new measure of teacher-rated anxiety disorder symptoms in children.

Hypothesis:

  1. A CBT oriented intervention as delivered by school personnel will be superior to an attention control procedure in reducing anxiety symptoms in at-risk children.
  2. Children who have parental involvement will post stronger and more enduring treatment gains.
Registry
clinicaltrials.gov
Start Date
November 2002
End Date
June 2005
Last Updated
20 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Children enrolled in school between the ages of 7 and 13 who display anxiety symptoms.
  • Anxiety disorder symptoms (identified by a score of 56 or higher on the MASC; and teacher report, and /or parent recommendation) as the primary presenting problem. An enrolled child must have at least 2 of these criterions.
  • Fluency in English.
  • Parent willingness to sign consent form and to complete required assessments.
  • Student willingness to participate (child assent) in 10-week affective education program and completion of required assessments.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Anxiety symptoms

Study Sites (1)

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