Overview

This trial is active, not recruiting.

Condition sexual behavior
Treatment reducing the risk
Sponsor Mathematica Policy Research, Inc.
Start date August 2013
End date September 2016
Trial size 2220 participants
Trial identifier NCT02054026, PRP699102

Summary

The purpose of this study is to evaluate the effectiveness of an eight-hour version of Reducing the Risk on outcomes such as sexual initiation, condom and contraceptive use, number of sexual partners, and pregnancy.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification efficacy study
Intervention model parallel assignment
Masking open label
Primary purpose prevention
Arm
(Experimental)
An eight-lesson (approximately eight-hour) version of Reducing the Risk
reducing the risk
(No Intervention)

Primary Outcomes

Measure
Sexual Initiation
time frame: 2-years post intervention

Secondary Outcomes

Measure
Sexual Initiation
time frame: 1-year post intervention
Contraceptive use
time frame: 1-year post intervention
Contraceptive use
time frame: 2-years post intervention
Number of sexual partners
time frame: 1-year post intervention
Number of sexual partners
time frame: 2-years post intervention

Eligibility Criteria

Male or female participants of any age.

Inclusion Criteria: - 9th grader - Attends participating school

Additional Information

Official title Impact Evaluation of the Reducing the Risk Program
Trial information was received from ClinicalTrials.gov and was last updated in September 2015.
Information provided to ClinicalTrials.gov by Mathematica Policy Research, Inc..