Active Bystander Training to Reduce Sexual Violence
Safer Drinking Spaces Study
Recruiting
N/AInterventional Study
Sexual ViolenceBystander Intervention
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
3,180 (estimated)
Sponsor
RTI International · Other
Who this trial is looking for
This trial is looking for staff and patrons of bars to participate in a study about training to prevent sexual violence. Participants will share their experiences through surveys over about a year.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 18 years old
I can read and speak English
I am an employee or a patron of a participating venue
You may not be able to join if
I have a condition that would prevent me from giving informed consent
I have a condition that would make my participation unsafe
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
The goal of this study is to evaluate the active bystander training provided by Safe Bars, Inc. and their local chapter organizations to staff at alcohol-serving establishments (e.g., bars). The training aims to improve norms about violence, create safer environments by teaching staff to intervene in potentially harmful situations, and help prevent sexual violence in the venue community. The study…
The goal of this study is to evaluate the active bystander training provided by Safe Bars, Inc. and their local chapter organizations to staff at alcohol-serving establishments (e.g., bars). The training aims to improve norms about violence, create safer environments by teaching staff to intervene in potentially harmful situations, and help prevent sexual violence in the venue community. The study will examine the implementation and effectiveness of the training. The main questions it aims to answer are:
1. Do staff and patrons at venues that have received Safe Bars training experience lower rates of sexual violence at the venue than staff and patrons at venues that have not received the training?
2. Are staff at venues that have received Safe Bars training more likely to intervene in potentially risky situations than staff at venues that have not received the training?
3. What characteristics of venue environments and staff and patron beliefs and perceptions are responsible for effects of the training on sexual violence and bystander behavior outcomes?
4. What characteristics and conditions are necessary for effective Safe Bars implementation and improved staff and patron outcomes?
Researchers will compare staff and patron experiences at venues that have received the training with venues that are offered a delayed training. Staff and patron participants will be asked to complete surveys over about 12 months, research staff will conduct observations of training and observations in the venues, and selected venue managers and staff will be asked to complete individual interviews.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* At least 18 years old
* Able to read and speak English
* Employee or patron of participating venues
Exclusion Criteria:
* Has any condition that, in the opinion of the PI or their designee, would preclude informed consent, make study participation unsafe, complicate interpre…
Inclusion Criteria:
* At least 18 years old
* Able to read and speak English
* Employee or patron of participating venues
Exclusion Criteria:
* Has any condition that, in the opinion of the PI or their designee, would preclude informed consent, make study participation unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives.
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