- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07434856
Evaluation of a Sexual Violence and Intimate Partner Violence Primary Prevention Program Implemented in Drinking Establishments
February 19, 2026 updated by: Jamila K. Stockman, University of California, San Diego
The Safe Night Out Evaluation Study: Evaluation of a Sexual Violence and Intimate Partner Violence Primary Prevention Program Implemented in Drinking Establishments
The goal of this project is to evaluate the effectiveness of Safe Night Out, a community-level primary violence prevention program offered in drinking establishments in the Sacramento region of California.
The main questions this project aims to answer are: 1) Does the Safe Night Out program reduce incidents of sexual violence and intimate partner violence among patrons?
2) Does the Safe Night Out program increase incidents of safety checks of patrons by staff participants?
To address these questions, we will enroll 150 staff participants and 500 patron participants from 25 drinking establishments that have implemented the Safe Night Out program (~3 staff participants and 10 patron participants per drinking establishment) and 25 drinking establishments that have not implemented the Safe Night Out program (~3 staff participants and 10 patron participants per drinking establishment).
Participants will complete a baseline and three 6-month follow-up assessments, until 18 month-follow-up.
Study Overview
Status
Not yet recruiting
Intervention / Treatment
Detailed Description
The overarching goal of this project is to evaluate the effectiveness of Safe Night Out (SNO), a community-level primary prevention program offered in drinking establishments in the Sacramento region of California.
Developed and implemented in 2019 by WEAVE, Inc., Sacramento County's primary domestic violence (DV) provider, SNO aims to train nightlife staff on how to recognize warning signs of sexual violence (SV) and intimate partner violence (IPV), and how to respond through active bystander skills to keep patrons safe.
SNO has been tailored for drinking establishments in neighborhoods with high rates of SV and IPV.
SNO, a single session education and bystander skills training, is to our knowledge, the only program implemented in drinking establishments in these neighborhoods.
Guided by Social Cognitive Theory, Social Norms Theory, and the Bystander Education Model, and in collaboration with our Research Advisory Board, our community-academic team will conduct a quasi-experimental mixed methods evaluation study using a comparative time-interrupted series design.
This study is a nonrandomized, quasi-experimental evaluation of an existing community-based violence prevention program.
The research team will not prospectively assign individuals or establishments to intervention conditions; rather, outcomes are evaluated in relation to the naturalistic rollout of the Safe Night Out program implemented by a community partner.
The aim of the study is to determine the effectiveness of SNO on increasing bystander intervention and reducing SV and IPV at the individual-level (e.g., patrons, staff) and population-level (e.g., census block).
Individual-level primary outcomes among patrons include past 6-month SV and past 6-month IPV victimization and perpetration; secondary outcomes among staff include past 6-month increase in bystander intervention and safety checks in drinking establishments.
We will also determine the effectiveness of SNO on 2-year average rates of rape, domestic violence assault and domestic violence police calls.
We will enroll 25 drinking establishments in the queue at WEAVE to receive SNO training and identify 25 drinking establishments who will not receive the SNO training during the study period.
This will allow for comparison between the two groups based on individual-level and staff-level outcomes, before (3 months prior) and after SNO program training (6, 12, and 18-month follow-up) using quantitative survey data (n=500 patrons, 10 per establishment and n=150 staff, 3 per establishment).
Study Type
Observational
Enrollment (Estimated)
650
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jamila K. Stockman, PhD, MPH
- Phone Number: 858-822-4652
- Email: jstockman@health.ucsd.edu
Study Contact Backup
- Name: Maryam Hussain, PhD
- Email: m2hussain@health.ucsd.edu
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Drinking establishments will be identified from a pre-created list that identifies drinking establishments (e.g., bars, clubs) that have received SNO training in the past two years and drinking establishments that have not received SNO training.
Staff and patron participants will be recruited from the identified drinking establishments in the Sacramento region of California.
Description
Inclusion Criteria:
- Aged 21 years or older (as required per California law for alcohol servers)
- Employed and working as a bar owner, manager, or staff member of the drinking establishment that has been recruited for the study (for staff participants)
- A customer or patron in the past month at the drinking establishment that has been recruited for the study (for patron participants)
- Ability to speak and understand English
Exclusion Criteria:
- Aged 20 years and under
- Inability to speak and understand English
- No current employment at a drinking establishment recruited for the study (for staff participants)
- No history of visiting the drinking establishment in the past month (for patron participants)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Staff participants plus Safe Night Out
Staff participants from drinking establishments where Safe Night Out has been implemented
|
A community-level primary violence prevention program offered in drinking establishments.
|
|
Staff participants no Safe Night Out
Staff participants from drinking establishments where Safe Night Out has not been implemented
|
No administration of the Safe Night Out program in drinking establishments.
|
|
Patron participants plus Safe Night Out
Patron participants from drinking establishments where Safe Night Out has been implemented
|
A community-level primary violence prevention program offered in drinking establishments.
|
|
Patron participants no Safe Night Out
Patron participants from drinking establishments where Safe Night Out has not been implemented
|
No administration of the Safe Night Out program in drinking establishments.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sexual Violence Victimization
Time Frame: Past six months
|
Self-reported
|
Past six months
|
|
Sexual Violence Perpetration
Time Frame: Past six months
|
Self-report
|
Past six months
|
|
Intimate Partner Violence Victimization
Time Frame: Past six months
|
Self-report, Conflict Tactics Scale (Revised)
|
Past six months
|
|
Intimate Partner Violence Perpetration
Time Frame: Past six months
|
Self-report, Conflict Tactics Scale (Revised)
|
Past six months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Safety Checks
Time Frame: Six-month follow-up assessments
|
Self-reported use of safety checks to prevent violence
|
Six-month follow-up assessments
|
|
Bystander intervention
Time Frame: Six-month follow-up assessments
|
Self-report of number of times active intervention occurred
|
Six-month follow-up assessments
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Jamila K. Stockman, PhD, MPH, University of California, San Diego
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
June 1, 2026
Primary Completion (Estimated)
December 1, 2028
Study Completion (Estimated)
December 1, 2028
Study Registration Dates
First Submitted
February 19, 2026
First Submitted That Met QC Criteria
February 19, 2026
First Posted (Actual)
February 27, 2026
Study Record Updates
Last Update Posted (Actual)
February 27, 2026
Last Update Submitted That Met QC Criteria
February 19, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- 813932
- U01CE003735 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Although the data are sensitive in nature, as they include information on sexual and intimate partner violence, drinking behavior, and police calls, the grant requires all data be made publicly available within 30 months of data collection completion.
De-identified data will be made publicly available on an appropriate data sharing repository.
IPD Sharing Time Frame
The grant requires all data be made publicly available within 30 months of data collection completion.
Datasets will be preserved for a minimum of 3 years following project closeout to support replication and secondary use requests approved Data Use Agreements.
IPD Sharing Access Criteria
The Data Steward (Dr.
Maryam Hussain) will oversee the Qualtrics data logs and ensure quality assurance of those data.
Dr Hussain will also create an analysis plan, including all steps for data cleaning and validation, that will become part of the data repository.
IPD Sharing Supporting Information Type
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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