Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID06443541

Strategies for Implementing GlobalConsent to Prevent Sexual Violence in University Men Across Seven Vietnamese Universities

Led by Emory University · Updated on 2025-08-05

3439

Participants Needed

7

Research Sites

N/A

Total Duration

On this page

Sponsors

E

Emory University

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to compare different methods for delivering GlobalConsent, a web-based program designed to prevent sexual violence, to men attending seven universities across Vietnam. The study focuses on evaluating lower-intensity versus higher-intensity strategies to implement this program, assessing how well each approach is followed, its effectiveness, and cost-effectiveness. The project addresses a critical adolescent risk factor by promoting healthier behaviors and informing national strategies to reduce sexual violence. The trial includes multiple groups such as students, faculty, university leaders, and implementation team members, each receiving materials and training based on their university's assigned implementation strategy. Students in the higher-intensity group get in-person orientations, monthly learning sessions, and frequent reminders, while those in the lower-intensity group receive basic email and text reminders for 12 weeks. Faculty and leaders receive access to educational content, webinars, and communication tailored by group intensity, and implementation teams receive training and support varying by strategy level. Participants will be monitored through surveys and assessments at baseline and multiple follow-up points up to 49 months, measuring behaviors related to sexual violence, attitudes, knowledge, and mental health. Researchers will track students' reported prosocial bystander actions and sexually violent behavior every six months for up to 30 months. Additional measures include perceptions of campus attitudes, acceptability and feasibility of the program, and mental health screenings. The study incorporates rigorous data collection to evaluate implementation success and participant outcomes over several years.

CONDITIONS

Brief Title

Strategies for Implementing GlobalConsent to Prevent Sexual Violence in University Men

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be a man aged 18 years or older
  • Self-identify as heterosexual or bisexual (attracted to women)
  • Be enrolled as a first-year student at one of the seven participating universities in Vietnam
  • Faculty members registered at the participating universities are eligible for faculty surveys
  • University leaders recommended by study staff with knowledge of implementation
  • Implementation team members identified by study staff
Not Eligible

You will not qualify if you...

  • Adults unable to provide consent
  • Individuals under 18 years old (infants, children, teenagers) for student participation
  • None for faculty, leaders, or implementation team members

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or online) for eligibility assessment and consent

Outpatient Treatment

Duration - Approximately 3 months of active program engagement

Participants engage in GlobalConsent prevention programs with different implementation strategies depending on their group assignment: students receive educational outreach and program sessions; faculty, leaders, and implementation team members receive various levels of access to educational materials, training, and webinars.

Multiple program sessions and communications over 12 weeks, including orientation, monthly sessions, email/SMS reminders, webinars, and trainings depending on participant role

Long-term Monitoring

Duration - Up to 49 months

Participants complete surveys and assessments to evaluate program effectiveness and implementation outcomes up to 49 months.

Assessments at baseline and at scheduled intervals up to 49 months, including every 6 months for some measures

Trial Site Locations

Total: 7 locations

1

Can Tho University of Medicine and Pharmacy (CTUMP)

Can Tho, Vietnam

Actively Recruiting

2

Da Nang University of Medical Technology & Pharmacy (DUMTP)

Da Nang, Vietnam

Actively Recruiting

3

Hai Phong University of Medicine and Pharmacy

Haiphong, Vietnam

Actively Recruiting

4

Hanoi Medical University

Hanoi, Vietnam, 116001

Actively Recruiting

5

Ho Chi Minh City Medicine and Pharmacy University

Ho Chi Minh City, Vietnam

Actively Recruiting

6

Hong Bang University

Ho Chi Minh City, Vietnam

Actively Recruiting

7

Hue University of Medicine and Pharmacy

Huế, Vietnam, 470000

Actively Recruiting

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Research Team

K

Kathryn Yount, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

4

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Published Research Related To This Trial

Strategies for Implementing GlobalConsent to Prevent Sexual Violence in University Men (SCALE): Study Protocol for a National Implementation Trial.

Kathryn M Yount, Daniel Whitaker, Xiangming Fang...

https://pubmed.ncbi.nlm.nih.gov/39315253

Strategies for Implementing GlobalConsent to Prevent Sexual Violence in University Men (SCALE): study protocol for a national implementation trial.

Kathryn M Yount, Daniel J Whitaker, Xiangming Fang...

https://pubmed.ncbi.nlm.nih.gov/39210388