Evaluation of the Teen Outreach Program in Chicago Public Schools

Status Completed

Clinical Trial Summary

The purpose of this study was to determine the impact of TOP® on sexual health behavior.

Clinical Trial Description

The cluster-randomized study was conducted in 9th grade classrooms in Chicago Public Schools (CPS) with equal number of schools randomized to intervention and comparison groups for two cohort years. Students were administered a scannable paper survey at three time points: baseline, post-program and 1-year post program. The primary impact analysis used an intent-to-treat approach. Implementation of TOP® was assessed by conducting classroom observations. TOP® was delivered in a variety of classroom settings over the school year by facilitators from CPS and partner organizations. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Sexual Behavior

Clinical Trial Details

NCT number	NCT02548871
Study type	Interventional
Source	Chapin Hall Center for Children
Contact
Status	Completed
Phase	N/A
Start date	September 2010
Completion date	August 2015

View Details

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