BridgeMD
New treatment option for Violence, Sexual
Official title Strategies for Implementing GlobalConsent to Prevent Sexual Violence in University Men
ClinicalTrials.gov ID: NCT06443541
What this study is testing
- What it's testing
- This project, SCALE, will be the first to compare lower-intensity (standard) and higher-intensity implementation strategies to deliver GlobalConsent-an efficacious web-based sexual violence prevention program-to men attending seven universities across Vietnam. Following a rigorous, mixed-methods, comparative interrupted-time-series design, researchers will collect novel data to compare implementation fidelity, drivers and outcomes, effectiveness, and cost-effectiveness across implementation strategy groups.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older. Healthy volunteers may be eligible.
You may be able to join if
- for Students:
- 18 and older
- Men who self-identify as heterosexual or bisexual (who are attracted to women),
- Enrolled as first-year students in any of the seven participating study universities in North, Central, and South Vietnam.
You likely can't join if
- for Students:
- Adults unable to consent
- Individuals who are not yet adults (infants, children, teenagers) Inclusion Criteria for Faculty:
- All registered lecturers at each of the seven participating study universities will be eligible to participate in the faculty surveys in years 1, 3...
- None Inclusion Criteria for Leaders:
- Recommendation of study staff at each participating study university
See the full eligibility criteria
- for Students:
- 18 and older
- Men who self-identify as heterosexual or bisexual (who are attracted to women),
- Enrolled as first-year students in any of the seven participating study universities in North, Central, and South Vietnam.
- for Students:
- Adults unable to consent
- Individuals who are not yet adults (infants, children, teenagers) Inclusion Criteria for Faculty:
- All registered lecturers at each of the seven participating study universities will be eligible to participate in the faculty surveys in years 1, 3, and 5. Exclusion Criteria for Faculty:
- None Inclusion Criteria for Leaders:
- Recommendation of study staff at each participating study university
- Knowledge about the implementation landscape and implementation of GlobalConsent. Exclusion Criteria for Leaders:
- None Inclusion Criteria for Implementation Teams:
- Identified by relevant study staff. Exclusion Criteria for Implementation Teams:
- None
The study team makes the final eligibility decision.
Where it's taking place
- Can Tho, Vietnam
- Da Nang, Vietnam
- Haiphong, Vietnam
- Hanoi, Vietnam
- Ho Chi Minh City, Vietnam
- Huế, Vietnam
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Can Tho, Vietnam; Da Nang, Vietnam; Haiphong, Vietnam; Hanoi, Vietnam; Ho Chi Minh City, Vietnam; Huế, Vietnam. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.