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Impact Evaluation of the Reducing the Risk Program

NCT02054026 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2220

Last updated 2017-04-17

No results posted yet for this study

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.

Conditions

  • Sexual Behavior

Interventions

BEHAVIORAL

Reducing the Risk

Sponsors & Collaborators

  • Mathematica Policy Research, Inc.

    lead OTHER

Principal Investigators

  • Robert Wood, PhD · Mathematica Policy Research

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-08-31
Primary Completion
2016-12-31
Completion
2016-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02054026 on ClinicalTrials.gov