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Clinical Trials/NCT02437968
NCT02437968
Completed
Not Applicable

Disseminating Evidence-based Practice to the Schools: CBT for Child Anxiety

Temple University0 sites76 target enrollmentDecember 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anxiety Disorders
Sponsor
Temple University
Enrollment
76
Primary Endpoint
Change in the number of children treated for anxiety.
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The present study aims to test the implementation and sustainability of (a) a Computer-Assisted Cognitive-Behavioral Treatment (CACBT) for youth anxiety and (b) the BASC-2 TRS to identify anxious youth in the school setting using a cohort-sequential design (i.e., three years at 20 schools over the span of five years).

'Camp Cope-A-Lot (Computer-assisted CBT program)'

Detailed Description

The present study will test the implementation and sustainability of (a) a Computer-Assisted Cognitive-Behavioral Treatment (CACBT) for youth anxiety and (b) the BASC-2 TRS to identify anxious youth in the school setting using a cohort-sequential design (i.e., three years at 20 schools over the span of five years). There are 3 phases: Phase I (baseline): Gather data on prevalence and services provided via screening measures and treatment trackers: Phase II (implementation): Train school staff in the identification of anxious youth (i.e. BASC-2 TRS) and the provision of the intervention (i.e., CACBT), modifying assessment and treatment procedures so as to best fit each individual school. Identify barriers and facilitators of implementation by gathering the qualitative experience of school staff: Phase II (sustainability): Discontinue training and supervision. Assess sustainability of the assessment and intervention. Identify barriers and facilitators of implementation by gathering the qualitative experience of school staff. 'Camp Cope-A-Lot (Computer-assisted CBT program)"

Registry
clinicaltrials.gov
Start Date
December 2010
End Date
June 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All mental health workers (e.g., guidance, social work, school psychologists) in the schools will be eligible to be trained.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Change in the number of children treated for anxiety.

Time Frame: Baseline, end of year 1, end of year 2, end of year 3

Change in the number of children identified as anxious.

Time Frame: Baseline, end of year 1, end of year 2, end of year 3

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