CompletedNot Applicable

Evaluation of Safer Sex Intervention (SSI)

319 participantsStarted 2012-02

Plain-language summary

The purpose of the study is to determine the impact of the offer to participate in Safer Sex Intervention (SSI) (treatment) relative to the offer to participate in Female Sexual Health (control) on three self-reported sexual behaviors (condom use, other contraceptive use, and frequency of sex) six months after the end of treatment.

Who can participate

Age range14 Years – 19 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: Between the ages of 14-19 Had engaged in sex with a male in the three months prior to enrollment Provide parental consent (if under age 18) and participant assent to participate in the study. Exclusion Criteria: Not have previously participated in any of the following pregnancy/HIV prevention programs: * 4 Real Health * Becoming a Responsible Teen (BART) * Healthy Living * Staying Mature and Responsible Towards Sex (SMARTS) * Sisters Informing Healthy Living and Empowering (SIHLE) * Project AIM * Making Proud Choices * Be Proud Be Responsible * Focus on Your Future

What they're measuring

Two questionnaire items measuring consistency of condom use

Timeframe: 6 months after the end of intervention

Trial details

NCT IDNCT02544841

SponsorThe Policy & Research Group

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2015-10

View on ClinicalTrials.gov More Teen Pregnancy Prevention trials