The goal of this trial is to test a modified mobile health intervention (with a group component) relative to a mobile health intervention in a two-arm randomized trial with up to 500 young women who are human immunodeficiency virus (HIV)-negative and who misuse alcohol. The expected outcomes are to: (1) determine the efficacy of the virtual group component in reducing alcohol use and sexual risk and increasing pre-exposure prophylaxis (PrEP) utilization; and (2) understand selected outcomes for implementation. Participants will be randomized to receive either the mHealth app or the mHealth app plus the group component, and followed up at 3- and 6-months post-enrollment.
Age range
18 Years – 30 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Alcohol (Biological)
Timeframe: Baseline
Alcohol (Biological)
Timeframe: 3-month
Alcohol (Biological)
Timeframe: 6-month
Alcohol (Biological)
Timeframe: Baseline
Alcohol (Biological)
Timeframe: 3-month
Alcohol (Biological)
Timeframe: 6-month
Alcohol (Self-Reported)
Timeframe: Baseline
Alcohol (Self-Reported)
Timeframe: 3-month
Alcohol (Self-Reported)
Timeframe: 6-month
Alcohol (Self-Reported)
Timeframe: Baseline
Alcohol (Self-Reported)
Timeframe: 3-month
Alcohol (Self-Reported)
Timeframe: 6-month
Sexual Risk: HIV (Biological)
Timeframe: Baseline
Sexual Risk: HIV (Biological)
Timeframe: 6-month
Sexual Risk (Self-reported)
Timeframe: Baseline
Sexual Risk (Self-reported)
Timeframe: 3-month
Sexual Risk (Self-reported)
Timeframe: 6-month
PrEP Utilization (Biological)
Timeframe: 3-month
PrEP Utilization (Biological)
Timeframe: 6-month
PrEP Utilization (Self-Reported)
Timeframe: Baseline
PrEP Utilization (Self-Reported)
Timeframe: 3-month
PrEP Utilization (Self-Reported)
Timeframe: 6-month