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Impact Evaluation of the Wise Guys Program

Impact Evaluation of the Wise Guys Program

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02052830
Enrollment
737
Registered
2014-02-03
Start date
2013-08-31
Completion date
2018-01-31
Last updated
2017-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sexual Behavior, Sexually Transmitted Infections

Brief summary

The purpose of this study is to evaluate the impact of the Wise Guys program on the delaying sexual initiation on adolescent males in Eastern Iowa.

Detailed description

This study uses a randomized controlled design to compare the impacts of the Wise Guys Program to the business-as-usual school curriculum. The Wise Guys multi-session curriculum is delivered in different formats that range in length from 5 to 12 weeks and topics covered include communication and masculinity, dating violence, abstinence and contraception, and sexually transmitted infections. Study participants are 7th grade boys attending a participating school in either the Davenport Iowa or North Scott Community school districts. 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.

Interventions

BEHAVIORALWise Guys

Multi-session curriculum delivered in different formats that range in length from 5 to 12 weeks and topics covered include communication and masculinity, dating violence, abstinence and contraception, and sexually transmitted infections.

Sponsors

Mathematica Policy Research, Inc.
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
MALE
Healthy volunteers
Yes

Inclusion criteria

* 7th grade student in participating schools * Male

Design outcomes

Primary

MeasureTime frame
Sexual initiation24 months post-intervention

Secondary

MeasureTime frame
Sexual initiation6 months post-intervention

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026