This study is a randomized controlled trial using a web-based adaptation of the RealConsent program among eligible college men in Hanoi, Vietnam. This study will test the impact of the program on promoting prosocial bystander behavior and preventing sexual violence perpetration, through improvements in the seven knowledge, attitudinal, and emotional mediators over a seven month study period, with a baseline survey and two follow-up surveys.
Age range
18 Years – 24 Years
Sex
MALE
See this in plain English?
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.
Number of Participants Reporting Contact Sexual Violence Via Physical Tactics
Timeframe: Baseline, immediately after completing the 3 week intervention, 6 months after completing the intervention
Number of Participants Reporting Contact Sexual Violence Via Non-physical Tactics
Timeframe: Baseline, immediately after completing the 3 week intervention, 6 months after completing the intervention
Number of Participants Reporting Non-contact Sexual Violence
Timeframe: Baseline, immediately after completing the 3 week intervention, 6 months after completing the intervention
Number of Participants Reporting Prosocial Bystander Behavior
Timeframe: Six months following baseline