A Healthy Relationships Program for Vulnerable Youth

Sexually Transmitted Diseases Clinical Trial

Official title: About Us: A Healthy Relationships Program for Vulnerable Youth

Status Completed

Clinical Trial Summary

Developed from a piloted intervention and based on scientific evidence, About Us is an innovative healthy relationships intervention that promotes positive adolescent romantic relationships and use of condoms and highly effective contraceptives if having sex. The program includes 10 lessons (2 that are between 30-45 minutes long 8 that are 50 minutes long) that blend group-based activities with online activities implemented in a small group format with students in grades 9 or 10 who have parental consent and provide assent to take part. The program will be implemented in school-based health centers (SBHCs).

Primary research question:

1. Nine months following the end of the program, what is the impact of About Us relative to the standard of care on:

1.1. Rates of vaginal or anal sex without condoms in the past three months?

Secondary research questions:

2. Three and nine months following the end of the program, what is the impact of About Us relative to the standard of care on:

2.1. Rates of abstinence from vaginal or anal sex in the past three months? 2.2. Frequency of communicating without abuse? 2.3. Utilization of school-based health center services? 2.4. Rates of behavioral willingness and attitudes toward birth control?

Exploratory research questions:

3. Three and nine months following the end of the program, what is the impact of About Us relative to the standard of care on:

3.1. The psychosocial variables stemming from the theoretical framework (e.g., attitudes toward condom and contraceptive use, normative beliefs, perceived self-efficacy to use condoms or have difficult conversations) and enumerated in the logic model.

3.2. Outcomes listed above within key sub-groups including those defined by sex (male/female), race/ethnicity, and exposure to violence;

4. Among those receiving About Us, how do effect sizes for the primary and secondary behavioral outcomes vary by dosage?

Clinical Trial Description

Students will be screened for eligibility through each school-based health center (SBHC) by SBHC staff, and those participants meeting the screening eligibility requirements (previous exposure to violence and/or previous or current involvement in a romantic relationship) will be offered a parental consent form and informational packet. Consent forms will be available in English and Spanish. Pending parental consent and youth assent, students will be randomized into either the intervention or control group. ;

Related Conditions & MeSH terms

• Pregnancy, Unplanned
• Sexually Transmitted Diseases

• NCT number: NCT03736876
• Study type: Interventional
• Source: ETR Associates
• Status: Completed
• Phase: N/A
• Start date: February 1, 2018
• Completion date: May 12, 2021