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

Sponsor
University of British Columbia (Other)
Overall Status
Completed
CT.gov ID
NCT00247754
Collaborator
Canadian Institutes of Health Research (CIHR) (Other)
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Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Cognitive Behaviour Treatment
N/A

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single
Primary Purpose:
Prevention
Official Title:
VP3: Vancouver Primary Prevention Program (Anxiety Disorders Prevention in School Children)
Study Start Date :
Nov 1, 2002
Study Completion Date :
Jun 1, 2005

Outcome Measures

Primary Outcome Measures

  1. Anxiety symptoms []

Eligibility Criteria

Criteria

Ages Eligible for Study:
7 Years to 13 Years
Sexes Eligible for Study:
All
Accepts 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.

Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of British Columbia, Faculty of Education Vancouver British Columbia Canada V6T 1Z4

Sponsors and Collaborators

  • University of British Columbia
  • Canadian Institutes of Health Research (CIHR)

Investigators

  • Principal Investigator: Lynn Miller, PhD, R.Psych., University of British Columbia

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00247754
Other Study ID Numbers:
  • B01-0072
First Posted:
Nov 2, 2005
Last Update Posted:
Nov 2, 2005
Last Verified:
Oct 1, 2005
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 2, 2005