Skip to main content
Clinical Trials/NCT03729726
NCT03729726
Unknown
Not Applicable

A Randomized Controlled Trial Study of the Future Foundation 2.0 Personal Responsibility Education Innovative Strategies (PREIS) Program

Metis Associates, Inc.1 site in 1 country700 target enrollmentMay 11, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Teen Pregnancy
Sponsor
Metis Associates, Inc.
Enrollment
700
Locations
1
Primary Endpoint
Post measure of risk of exposure to sexually transmitted infections in the past 3 months
Last Updated
7 years ago

Overview

Brief Summary

This study uses a randomized controlled trial (RCT) design to evaluate the impacts of the Future Foundation (FF) 2.0 Personal Responsibility Education Innovative Strategies (PREIS) program on reducing students' sexual activity (vaginal), recent risking sexual activity without condom use, and unprotected sex (no condoms/contraceptives). FF will implement the 2.0 PREIS Program with three cohorts of African-American youth in the 6th to 8th grades. FF aims to recruit and enroll 400 students who are new to the program for Cohort 1, 150 new students for Cohort 2, and another 150 new students for Cohort 3. These cohorts of eligible students will come from grades 6-8 in Woodland and McNair middle schools and projected to attend Banneker high school. Random assignment will be an ongoing process throughout the project enrollment periods. By the end of the recruitment processes, a total of 700 students will be randomly assigned to either the treatment or the control group, resulting in 350 students in each condition. Each year, the FF 2.0 PREIS intervention model will offer year-round grant-funded services, including after-school, summer programming, and parent engagement activities. The 350 youth randomly assigned to the treatment group will be offered the FF 2.0 PREIS program (Cohort 1 will target 200 treatment youth from January 2018 through June 2018; Cohort 2 will target 75 treatment youth from August 2018 through May 2019; and Cohort 3 will serve 75 treatment youth from August 2019 through May 2020.), while the 350 students assigned to the control group may receive after school and/or summer programming from another community-based organization. The primary hypotheses for the RCT study are the following: significantly fewer numbers of students in the FF 2.0 PREIS intervention engage in vaginal sex than their control group peers do by the time of the end of the program and also at the six-month follow-up; significantly fewer numbers of students in the FF 2.0 PREIS intervention engage in recent unprotected sex significantly than the control group students do at the end of the program and also at the six-month follow-up; and significantly greater numbers of participants in the FF 2.0 PREIS intervention remain abstinent or report condom use during recent vaginal sexual activity than the control group students do at the end of the program and also at the six-month follow-up.

Registry
clinicaltrials.gov
Start Date
May 11, 2017
End Date
October 2021
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Metis Associates, Inc.
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Schools: attending Woodland and McNair middle schools and projected to attend Banneker high school
  • Grade level: Grades 6-8
  • Race/ethnicity or tribe: 100% African American
  • Gender: 34% male and 66% female (based on current make-up of Future Foundation youth)
  • Risk characteristics: 93% of youth will come from low-income families (based on free lunch eligibility)
  • Other characteristics: The majority of target youth will also exhibit academic need. 81% will be below proficiency in English language arts and 90% will score not proficient in math. All recruited subjects will be new to Future Foundation services.

Exclusion Criteria

  • Students who have already received Future Foundation services

Outcomes

Primary Outcomes

Post measure of risk of exposure to sexually transmitted infections in the past 3 months

Time Frame: 12 months after baseline

A dichotomous measure collected at the end of the program based on self-report questionnaire.

Post measure of ever having unprotected vaginal sex in the past 3 months

Time Frame: 12 months after baseline

A dichotomous measure collected at the end of the program based on self-report questionnaire.

Post measure of ever having vaginal sex in the past 3 months

Time Frame: 12 months after baseline

A dichotomous measure collected at the end of the program based on self-report questionnaire.

Follow-up measure of ever having vaginal sex in the past 3 months

Time Frame: 18 months after baseline

A dichotomous measure collected six months after the end of program implementation based on self-report questionnaire.

Follow up measure of risk of exposure to sexually transmitted infections in the past 3 months

Time Frame: 18 months after baseline

A dichotomous measure collected six months after the end of program implementation based on self-report questionnaire.

Follow up measure of ever having unprotected vaginal sex in the past 3 months

Time Frame: 18 months after baseline

A dichotomous measure collected six months after the end of program implementation based on self-report questionnaire.

Study Sites (1)

Loading locations...

Similar Trials