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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00247754
Enrollment
281
Registered
2005-11-02
Start date
2002-11-30
Completion date
2005-06-30
Last updated
2005-11-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety

Keywords

Anxiety, Therapy, Behaviour

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.

Interventions

BEHAVIORALCognitive Behaviour Treatment

Sponsors

Canadian Institutes of Health Research (CIHR)
CollaboratorOTHER_GOV
University of British Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
7 Years to 13 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Anxiety symptoms

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026