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

Not Applicable

Completed

• Conditions: Anxiety

• Registration Number: NCT00247754
• Lead Sponsor: University of British Columbia

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2002-11
• Study Completion: 2005-06
• Status Verified: 2005-10
• Study First Submitted: 2005-10-31
• Study First Submitted QC: 2005-10-31
• Last Update Submitted: 2005-10-31
• Study First Posted: 2005-11-02
• Last Update Posted: 2005-11-02

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 281

Inclusion Criteria

Children enrolled in school between the ages of 7 and 13 who display anxiety symptoms.

1. 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.
2. Fluency in English.
3. Parent willingness to sign consent form and to complete required assessments.
4. Student willingness to participate (child assent) in 10-week affective education program and completion of required assessments.

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Anxiety symptoms

Trial Locations

Locations (1)

University of British Columbia, Faculty of Education; 🇨🇦 Vancouver, British Columbia, Canada