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

Primary Purpose

Anxiety

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Cognitive Behaviour Treatment
Sponsored by
University of British Columbia
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Anxiety focused on measuring Anxiety, Therapy, Behaviour

Eligibility Criteria

7 Years - 13 Years (Child)All SexesDoes not accept healthy volunteers

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:

Sites / Locations

  • University of British Columbia, Faculty of Education

Outcomes

Primary Outcome Measures

Anxiety symptoms

Secondary Outcome Measures

Full Information

First Posted
October 31, 2005
Last Updated
October 31, 2005
Sponsor
University of British Columbia
Collaborators
Canadian Institutes of Health Research (CIHR)
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1. Study Identification

Unique Protocol Identification Number
NCT00247754
Brief Title
VP3: Vancouver Primary Prevention Program (Anxiety Disorders Prevention in School Children)
Official Title
VP3: Vancouver Primary Prevention Program (Anxiety Disorders Prevention in School Children)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2005
Overall Recruitment Status
Completed
Study Start Date
November 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
June 2005 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
University of British Columbia
Collaborators
Canadian Institutes of Health Research (CIHR)

4. Oversight

5. Study Description

Brief Summary
Objective: To evaluate the efficacy of a school-based cognitive behavior therapy (CBT) program in reducing anxiety disorder symptoms in at-risk public school children. To determine whether parent education and involvement improves outcome in anxious children treated with CBT. 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 To evaluate a new measure of teacher-rated anxiety disorder symptoms in children. Hypothesis: 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. Children who have parental involvement will post stronger and more enduring treatment gains.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety
Keywords
Anxiety, Therapy, Behaviour

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Single
Allocation
Randomized
Enrollment
281 (false)

8. Arms, Groups, and Interventions

Intervention Type
Behavioral
Intervention Name(s)
Cognitive Behaviour Treatment
Primary Outcome Measure Information:
Title
Anxiety symptoms

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
No
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:
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lynn Miller, PhD, R.Psych.
Organizational Affiliation
University of British Columbia
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of British Columbia, Faculty of Education
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V6T 1Z4
Country
Canada

12. IPD Sharing Statement

Learn more about this trial

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

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