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Evaluation of the Positive Prevention PLUS Program

Evaluation of the Positive Prevention PLUS Program Teen Pregnancy Prevention Program

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02540278
Acronym
PP+
Enrollment
4267
Registered
2015-09-03
Start date
2013-08-31
Completion date
2014-10-31
Last updated
2015-09-03

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

Conditions

Pregnancy in Adolescence

Brief summary

This study aims to determine if the Positive Prevention PLUS teen pregnancy prevention program has an impact on abstinence, birth control use, and likelihood of becoming pregnant.

Detailed description

A clustered randomized controlled trial (CRCT) was employed where participating high school sites were randomly assigned either to a treatment group that implemented the Positive Prevention PLUS program or a control group. Students completed a self-administered survey at baseline (prior to program implementation) and a 6 month follow-up survey (post program implementation). Eligible students in the sample included all male and female 9th-grade students from 21 high schools enrolled in mandatory 9th-grade health, science, or physical education classes, to which the district assigns students randomly. Of the 7,042 eligible students, 4,267 received parental consent and were enrolled in the study. Outcome variables include initiation of sexual activity, ever been pregnant, and birth control use.

Interventions

BEHAVIORALPositive Prevention PLUS

PP+ has elven 45 minute lessons: (1) Getting Started, (2) Life Planning, (3) Healthy Relationships, (4) Relationship Violence, (5) Family Planning and Contraceptives, (6) Myths and Stereotypes, (7) HIV Disease and AIDS, (8) Recognizing and Reducing Risk, (9) Peer and Media Pressures, (10) Human Immunodeficiency Virus (HIV)/Sexually Transmitted Disease (STD) Testing and Community Resources, and (11) Steps to Success.

Sponsors

Department of Health and Human Services
CollaboratorFED
California State University, San Bernardino
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Years to 19 Years
Healthy volunteers
Yes

Inclusion criteria

* Must have parental consent and be in the eligible school sites.

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Ever had sex (Yes/No)6 monthsEver had sex (Yes/No)
Ever been pregnant (Yes/No)6 monthsEver Been Pregnant (or gotten someone pregnant) (Yes/No)
Sex without using birth control in prior 3 months (Yes/No)6 monthsEver had sex without using birth control in prior 3 months (Yes/No)

Countries

United States

Outcome results

None listed

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