Impact Evaluation of the Teen Choice Program

Status Active, not recruiting

Clinical Trial Summary

The purpose of this study is to evaluate the impact of the Teen Choice program on reducing the rates of unprotected sex of high risk youth in New York.

Clinical Trial Description

This study uses a randomized controlled design to compare the impacts of the Teen Choice Program to the "business-as-usual" school curriculum. The Teen Choice curriculum is designed for adolescents aged 12 to 19 and will be delivered in different formats that range in length from 6 to 12 weeks. Teen Choice will be offered during the regular school day to middle and high school aged youth. This study is being conducted as part of the national Personal Responsibility Education Program evaluation funded by Administration for Children and Families within the U.S. Department of Health and Human Services. ;

Study Design

Related Conditions & MeSH terms

Sexual Behavior

Clinical Trial Details

NCT number	NCT02059486
Study type	Interventional
Source	Mathematica Policy Research, Inc.
Contact
Status	Active, not recruiting
Phase	N/A
Start date	January 2014
Completion date	June 2018

View Details

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