Expanding HIV Testing and Prevention to Reach Vulnerable Young Women
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Condomless Sex
- Sponsor
- RTI International
- Enrollment
- 500
- Locations
- 1
- Primary Endpoint
- Increased Condom Use
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
This two-arm cluster randomized trial tested a gender-focused comprehensive HIV testing and counselling (HTC) program, the Young Women's Health CoOp (YWHC) with a standard HTC program and targeted female adolescents (aged 16-19) who use substances and have dropped out of school. To evaluate the process, the study examined the feasibility of using peer role models as recruiters and co-facilitators of the intervention and monitored fidelity to the intervention. Efficacy of the intervention on behavioral and biological outcomes, and on linkages to health services, through follow-up visits conducted 6- and 12-months post-enrollment was also assessed.
Detailed Description
The purpose of this study was to test a gender-focused comprehensive HIV testing and counselling (HTC) program, the Young Women's Health CoOp (YWHC) with a standard HTC program in 24 disadvantaged communities in Cape Town, South Africa. The researchers conducted community-level randomization across the 24 communities with balanced recruitment from predominantly Black African and predominantly Coloured communities. The aims of the study were: Aim 1. To train and evaluate adolescent peer role models to conduct community outreach with established outreach workers to recruit 500 out-of-school, substance-using female adolescents aged 16 to 19 for HIV testing and counseling (HTC) and to co-facilitate a gender-focused comprehensive HTC program. Aim 2. To test the efficacy of a young women's gender-focused comprehensive HTC program for reducing substance use, victimization, and sexual risk behavior (primary outcomes) and improving access to effective treatment and support services through linkages to care (substance abuse treatment, HIV, sexually transmitted infections \[STIs\], antenatal and reproductive health as secondary outcomes) relative to standard HTC for adolescent females. The Young Women's Health CoOp has been adapted from the South African Women's Health CoOp (WHC) and the North Carolina Young Women's CoOp (YWC) which was found acceptable in focus groups and maintained all the core elements of the evidence-based intervention. For this study, the intervention was co-facilitated by trained staff from the local communities. The intervention consisted of two 1.5-hour group workshops (sessions), each having several modules that are usually administered a week apart: Workshop 1: Developmental Issues and Alcohol and Other Drugs; Gender, Problem-Solving and Conflict Negotiation, Violence and Values and Becoming a Powerful Young Woman: and Workshop 2: STIs, HIV/AIDS, Prevention, Condoms and Role-play. After each session, each participant developed a risk-reduction personalized action plan (PAP). To maintain PAP goals and reduce decay of intervention effects over time, the staff conducted case management to help participants attain these personal goals. Participants completed baseline, 6-month follow-up and 12-month follow-up assessments, which included a survey and biological testing for substance use, pregnancy and HIV.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Self-identify as living in one of the 24 targeted disadvantaged communities
- •Between 16 and 19 years old
- •Has dropped out of school for at least 6 months
- •Is currently dropped out of school
- •Has not completed matric (high school diploma) or have an N3 Certificate (South Africa National Technical Certificate)
- •Reports consuming 2-3 alcoholic drinks at least once in the last 30 days or using illicit drugs at least once a week.
- •Reports unprotected sex with a male partner in the last 90 days
- •Is able to provide informed assent to participate or informed consent if emancipated or 18 years old
- •Has lived in targeted community for at least 6 months and plans to reside in the target community for the next year and provide verifiable locator information
Exclusion Criteria
- •Participant must be able to pass a cognitive test
Outcomes
Primary Outcomes
Increased Condom Use
Time Frame: 12 months after baseline
Reduced number of unprotected anal and vaginal sex acts in the past 90 days. Increased skillful condom communication as measured by the 3-item Condom Negotiation scale measured by the YRBA (Youth revised Risk Behavior Assessment)
Reduced Alcohol and Illicit Drug Use
Time Frame: 12 months after baseline
Self-reported frequency of alcohol and illicit drug use the past 30 days as measured by PRBA. Biological measures of drug use through urine drug tests and breathalyzer tests.
Reduced Violence and Victimization
Time Frame: 12 months after baseline
Self-reported recent emotional, physical, and sexual abuse in the past 6 months measured by the RRBA (WHC Revised Risk Behavior Assessment).
Reduced Sexual Risk
Time Frame: 12 months after baseline
Reduced drug or alcohol use prior to sex (impairment), self-reported number of casual partners, sex trading, and concurrent partners (defined ≥ 2 partners in past 90 days) measured by the PRBA (WHC Pretoria Risk Behavior Assessment
Secondary Outcomes
- Increased Advancement in Education and Job Training(12 months after baseline)
- Increased Access to Health Services(12 months after baseline)