A Healthy Relationships Program for Vulnerable Youth

About Us: A Healthy Relationships Program for Vulnerable Youth

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?

Study Overview

• Status: Completed
• Conditions: Sexually Transmitted Diseases; Pregnancy, Unplanned
• Intervention / Treatment: Behavioral: About Us

Detailed 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.

• Study Type: Interventional
• Enrollment (Actual): 550
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • California
    • Oakland, California, United States, 94612
      • California School Based Health Alliance
    • San Diego, California, United States, 92182
      • San Diego State University
    • Scotts Valley, California, United States, 95066
      • ETR

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 14 years to 18 years (Child, Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• The target population includes 9th or 10th grade students from participating schools who meet at least one of the following inclusion criteria based on their responses to a school-wide health assessment:

  1. prior exposure to violence;
  2. prior or current experience with a romantic relationship.

Any student answering "yes" to either criteria would be eligible to take part in the study. Only those who have parent consent and assent would be enrolled.

Exclusion Criteria:

• Those students without parental consent;
• If siblings are eligible to participate, the sibling who returns the signed consent form first will be admitted into the study. Any other eligible siblings will be excluded.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Prevention
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Treatment group; These students will receive About Us, an innovative, healthy relationship intervention. The program includes 10 lessons that blend group-based activities with online activities implemented in school-based health centers.	Behavioral: About Us; Each program session includes an initial soap opera-like story to build interest and illustrate key concepts, 2-3 group-based activities with reflection, individual app-based work on tablets to allow for personalization of the content, and a group-based debrief to reflect on the day and reinforce key messages. The group-based content is delivered by trained facilitators from the participating school-based health centers. The app-based content is housed on a secure website and accessed through tablets with unique log-ins for each participant. Activities are completed individually during the session (e.g., completing a poll; watching and responding to a brief video). Several lessons include homework activities that encourage communication between students and a caring adult.
No Intervention: Delayed intervention (control group); These students will receive the business-as--usual condition (e.g., the standard health education that is provided by the school during the study period), and will receive the intervention once the study period has concluded.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Rates of vaginal or anal sex without condoms	Reported number of times having had vaginal or anal sex without using condoms or insertive condoms.	9 months post intervention

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Rates of abstinence of vaginal or anal sex	Reported number of times having had vaginal or anal intercourse. Response options range from 1 "Never" and 5 "4 or more times".	3 months post intervention
Rates of abstinence of vaginal or anal sex	Reported number of times having had vaginal or anal intercourse. Response options range from 1 "Never" to 5 "4 or more times".	9 months post intervention
Frequency of communicating without abuse	Reported number of times communicating with a partner without abuse. Response options range from 1 "Never - this has never happened in your relationship" to 4 "Often: this has happened 6 times or more in your relationship".	3 months post intervention
Frequency of communicating without abuse	Reported number of times communicating with a partner without abuse. Response options range from 1 "Never - this has never happened in your relationship" to 4 "Often: this has happened 6 times or more in your relationship".	9 months post intervention
Clinic utilization	Number of times receiving services or information from school-based health center on contraception, pregnancy, abortion, or sexually transmitted diseases	3 months post intervention
Clinic utilization	Number of times receiving services or information from school-based health center on contraception, pregnancy, abortion, or sexually transmitted diseases.	9 months post intervention
Behavioral intentions to engage in sexual activity	4 items from the Sexual Behavior Index (SBI) that assess one's willingness and intention to engage in sex in the next 3 months. Response options range from 1-7 with lower scores indicating lower willingness or intentions to engage in sexual activity.	3 months post intervention
Behavioral intentions to engage in sexual activity	4 items from the Sexual Behavior Index (SBI) that assess one's willingness and intention to engage in sex in the next 9 months. Response options range from 1-7 with lower scores indicating lower willingness or intentions to engage in sexual activity.	9 months post intervention
Behavioral intentions to use condoms	Assessed using 3 items from the COMPAS Program Behavioral Intentions Scale designed to measure one's intentions to acquire, discuss, and use condoms before sex. Items response options range from 1-4 with higher scores indicating higher intentions to perform the health behavior.	3 months post intervention
Behavioral intentions to use condoms	Assessed using 3 items from the COMPAS Program Behavioral Intentions Scale designed to measure one's intentions to acquire, discuss, and use condoms before sex. Items response options range from 1-4 with higher scores indicating higher intentions to perform the health behavior.	9 months post intervention

Collaborators and Investigators

• Sponsor: ETR Associates
• Collaborators: San Diego State University; Family and Youth Services Bureau; California School-Based Health Alliance
• Investigators: Principal Investigator: Karin K Coyle, PhD, ETR; Principal Investigator: Pamela M Anderson, PhD, ETR

Publications and helpful links

General Publications

• Anderson P, Coyle K, Guinosso S, Ferrand JL, Owora A, Houghton RF, Walsh-Buhi E. Promoting Adolescent Healthy Relationships (The About Us Program): Protocol for a Randomized Clinical Trial. JMIR Res Protoc. 2021 Sep 1;10(9):e30499. doi: 10.2196/30499.

Study record dates

Study Major Dates

• Study Start (Actual): February 1, 2018
• Primary Completion (Actual): May 11, 2021
• Study Completion (Actual): May 12, 2021

Study Registration Dates

• First Submitted: August 22, 2018
• First Submitted That Met QC Criteria: November 7, 2018
• First Posted (Actual): November 9, 2018

Study Record Updates

• Last Update Posted (Actual): March 24, 2022
• Last Update Submitted That Met QC Criteria: March 22, 2022
• Last Verified: March 1, 2022

More Information

Terms related to this study

• Keywords: Adolescents; Teens; Randomized Controlled Trial; Teen Pregnancy; Youth; Sexually Transmitted Diseases; Sexually Transmitted Infections; Unintended Pregnancy; Healthy Relationships; Sexual Health Education; School-Based Health Center
• Additional Relevant MeSH Terms: Pathologic Processes; Infections; Communicable Diseases; Disease Attributes; Sexually Transmitted Diseases
• Other Study ID Numbers: 90 AP2682-01-00

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO
• IPD Plan Description: As part of our commitment to data security and confidentiality, IPD will not be shared outside the research team.

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No