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Evaluation of the Making Proud Choices! Teen Pregnancy Prevention Program

Evaluation of the Making Proud Choices! Teen Pregnancy Prevention Program

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04863326
Enrollment
2810
Registered
2021-04-28
Start date
2017-01-01
Completion date
2019-12-31
Last updated
2021-04-29

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

Conditions

Teen Pregnancy Prevention

Brief summary

Under contract to the Office of Population Affairs (OPA), Mathematica is conducting an impact study of the Making Proud Choices! (MPC) teen pregnancy prevention program. The impact study is designed to estimate the impact of MPC, compared to the business-as-usual condition, on risk and protective factors, sexual behaviors, and longer term health goals including pregnancy and sexually transmitted infections.

Detailed description

This evaluation used a cluster randomized controlled trial (RCT) design to assess the effectiveness of MPC, with schools within districts randomly assigned to one of two conditions: (1) MPC implemented by health educators, or (2) business as usual. In total, 31 school clusters were randomly assigned to condition, including roughly 2800 students, in four geographic areas across the U.S. The study was implemented over the course of three school years (2016-17, 2017-18 and 2018-19), with youth in each year considered a separate evaluation cohort, and with participating schools (and new cohorts of eligible youth) randomized to condition each year. There are two main sources of data for this study: outcome and implementation data. Youth in the study completed two waves of self-report surveys: (1) a baseline survey administered before programming began, and (2) a follow-up outcome survey administered approximately six months after the end of programming (approximately 9 months after baseline, on average). The surveys measured antecedents to sexual behavior (risk and protective factors), sexual behaviors, and ultimately, MPC's health goals of reducing sexually transmitted infections and teen pregnancies. Program implementation data included fidelity and attendance logs, observations, interviews, study youth focus groups, staff surveys, and technical assistance logs. The benchmark analytic approach for estimating program impacts focuses on individuals with observed (non-missing) outcome data, and will statistically adjust for several baseline and location variables to produce credible and precise estimates of program effectiveness. Several sensitivity analyses will be conducted to understand the robustness of the findings across alternative specifications, and to understand the effect of MPC across a variety of subgroups.

Interventions

Sponsors

Office of Population Affairs
CollaboratorUNKNOWN
Mathematica Policy Research, Inc.
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

The MPC curriculum aims to provide adolescents with the information and tools they need to reduce their risk of sexually transmitted diseases (STDs), HIV, and pregnancy. The curriculum emphasizes abstinence as the safest choice for avoiding pregnancy and STDs, but also encourages youth to use condoms and other methods of birth control if they do have sex. The curriculum includes video clips, student role-playing activities, and group discussions. It also involves skill-building activities for correct condom use, refusal techniques, and safer-sex negotiation, and opportunities for students to practice these skills.

Eligibility

Sex/Gender
ALL
Age
13 Years to 19 Years
Healthy volunteers
No

Inclusion criteria

* Enrolled in a study school * Attending the targeted class (e.g. health class) for the first time

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Any sex without a condom (in past 3 months)Survey administered 6 months post programBinary variable representing if respondent reported having any risk for STD/STI sex (sex without a condom) in the three month period before completing the follow-up survey.
Times having any sex without a condom in past 3 monthsSurvey administered 6 months post programCount variable representing the total number of times respondent had risky sex in the three months before completing follow-up survey.
Sex without birth control in past 3 monthsSurvey administered 6 months post programBinary variable representing if respondent reported having had unprotected vaginal sex in the three months before completing the follow-up survey.
Knowledge about HIVSurvey administered 6 months post programProportion of knowledge items about HIV/STDs answered correctly.
Knowledge about pregnancySurvey administered 6 months post programProportion of knowledge items about pregnancy answered correctly.
Knowledge about condomsSurvey administered 6 months post programProportion of knowledge items about condom use answered correctly.
Knowledge about other forms of contraceptionSurvey administered 6 months post programProportion of knowledge items about contraceptive use answered correctly.
Belief that sex may adversely affect future goalsSurvey administered 6 months post programProportion of statements about how sexual activity will interfere with goals and dreams that the respondent agrees or strongly agrees with.
Belief that condoms can be pleasurableSurvey administered 6 months post programProportion of statements about how condoms can be pleasurable that the respondent agrees or strongly agrees with.
Attitudes about condomsSurvey administered 6 months post programProportion of statements about condom use that the respondent either agrees or strongly agrees with.
Condom self-efficacySurvey administered 6 months post programProportion of statements about self-efficacy using condoms that the respondent agrees or strongly agrees with.
Condom negotiationSurvey administered 6 months post programProportion of statements about self-efficacy negotiating condom that the respondent agrees or strongly agrees with.
Refusal skillsSurvey administered 6 months post programProportion of statements about self-efficacy refusing sex with a partner that the respondent agrees or strongly agrees with.
Ever any sex (vaginal, oral, or anal)Survey administered 6 months post programBinary variable representing if the respondent reported having ever had vaginal, oral, or anal sex.
Any sex (in past 3 months)Survey administered 6 months post programBinary variable representing if the respondent reported having vaginal, oral, or anal sex in the three month period before completing the follow-up survey.
Times having any sex (in past 3 months)Survey administered 6 months post programCount variable representing the total number of times respondent had vaginal, oral and/or anal sex in the three month period before completing the follow-up survey.
Count of vaginal sex partners (in the past 3 months)Survey administered 6 months post programCount variable representing the number of partners for vaginal sex in the three month period before completing the follow-up survey.
Times having sex without birth control (in past 3 months)Survey administered 6 months post programCount variable representing the total number of times the respondent had unprotected vaginal sex in the three month period before completing the follow-up survey.
Ever pregnantSurvey administered 6 months post programBinary variable representing if the respondent reported a pregnancy or has gotten someone pregnant.
Any sexually transmitted infection (STI)Survey administered 6 months post programBinary variable representing if the respondent indicated having been told they have a sexually transmitted infection.

Outcome results

None listed

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