ClinicalTrials.Veeva

Menu

Impact Evaluation of the Reducing the Risk Program

M

Mathematica Policy Research

Status

Completed

Conditions

Sexual Behavior

Treatments

Behavioral: Reducing the Risk

Study type

Interventional

Funder types

Other

Identifiers

NCT02054026
PRP699102

Details and patient eligibility

About

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.

Enrollment

2,220 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • 9th grader
  • Attends participating school

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

2,220 participants in 2 patient groups

Reducing the Risk
Experimental group
Description:
An eight-lesson (approximately eight-hour) version of Reducing the Risk
Treatment:
Behavioral: Reducing the Risk
Control
No Intervention group

Trial contacts and locations

13

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems