A Phase 2 interventional study of Cross Cutting e-health Prevention Program Individual Interventions in Alcohol Misuse Prevention and Sexual Violence Prevention, sponsored by University of New Hampshire. Recruiting at 1 site in United States. Open to participants aged 18 Years to 24 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-22.
Sponsored by University of New Hampshire · Phase 2, Interventional, and Prevention
The National Institute of Health Academic Research Enhancement Award research study fills a major gap in sexual violence and alcohol misuse prevention on college campuses by implementing and testing the feasibility of a multi-level social ecological model approach consisting of six established e-health primary prevention strategies in a feasibility study.
The National Institute of Health Academic Research Enhancement Award Pilot Study fills a major gap in sexual violence and alcohol misuse prevention on college campuses by implementing and testing the feasibility of a multi-level approach consisting of six established e-health primary prevention strategies of a Cross Cutting e-health Prevention Program, with six evidence-based and proven alcohol misuse and sexual violence prevention strategies as a full package of synergistic cross-cutting interventions that target multiple levels of the social ecological model (individual, relationship, and community).
University of New Hampshire is the lead sponsor of 15 studies on the registry; 4 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Participants in the intervention arm will participate in the RealConsent serial webinar program, the +Change Social Norms Program, and the ShipHappens Bystander Video Game.
Behavioral: Cross Cutting e-health Prevention Program Individual Interventions
True control group.
Three sexual violence and alcohol misuse ehealth prevention programs for college students.
Also known as: RealConsent, +Change, ShipHappens
Sexual Experiences Survey-Short Form Victimization
Sexual assault victimization was assessed with Revised Sexual Experience Survey. Participants were asked how often they experienced 7 unwanted sexual experiences. Also, the tactic that was used (for example, "using force") was also noted. Response options ranged from 0 (never) to 3 (3 or more times). An overall score for the Revised Sexual Experience Survey, was calculated by Summing each Outcome and Tactic Score with a range from 0 to 135 with higher scores indicating more sexual violence victimization, a worse score than the lower scores. The second method combines several of the outcomes, but keeps tactics separate, resulting in a potential range of 0 to 63 with the higher score being a worse score than the lower score.
Time frame: Baseline, 8 weeks, 16 weeks
Sexual Experiences Survey-Short Form Perpetration
The Sexual Experiences Survey-Short Form Perpetration is a 7-item, behaviorally specific self-report instrument designed to assess the perpetration of unwanted sexual behaviors. It covers sexual coercion, unwanted contact, attempted rape, and rape, typically asking about acts committed since age 14 or in the past year. The higher score indicates more unwanted sexual experiences and therefore is a worse score than a lower score.
Time frame: Baseline, 8 weeks, 16 weeks
Alcohol Use Disorders Identification Test-Concise
The Alcohol Use Disorders Identification Test is a 10-item screening tool developed by the World Health Organization to assess alcohol consumption, drinking behaviors, and alcohol-related problems. The higher the score indicates more alcohol related problems, therefore a worse score.
Time frame: Baseline, 8 weeks, 16 weeks
Drinking Behavior Questionnaire
A ten-item self report measure looking at an individual's drinking habits. The higher the score indicates more problematic drinking habits, therefore a worse score.
Time frame: Baseline, 8 weeks, 16 weeks
Bystander Attitudes Scale Revised
12-item measure of attitudes towards bystander behaviors. Higher scores are better scores indicating that the participant is more willing to engage in prosocial bystander intervention before, during, or after sexual assault or violence situations.
Time frame: Baseline, 8 weeks, 16 weeks
Barriers to Sexual Assault Bystander Intervention Scale
The Barriers to Sexual Assault Bystander Intervention Scale is a 16-item, 7-point Likert-scale questionnaire that measures five key psychological barriers hindering bystander intervention in sexual violence. It assesses failure to notice, interpret risk, take responsibility, possess skills, or fear of negative evaluation. Higher scores are worse scores indicating greater perceived barriers to prosocial bystander intervention.
Time frame: Baseline, 8 weeks, 16 weeks
Social Self-identification Scale
4-item measure to assess the relevancy of the intervention to the participant's life. The higher score indicates that intervention was more relevant to the participant's life indicating a better score.
Time frame: 8 weeks, 16 weeks
Bystander Efficacy Scale
The Bystander Efficacy Scale measures the effectiveness of sexual violence prevention programs based on preventing antecedents to sexual violence by increasing prosocial bystander behavior. On this measure, participants are asked to indicate their confidence, on an 11-point scale, in performing each of the listed 14 bystander behaviors. Higher average scores are better scores indicating a person's greater bystander self-efficacy (higher confidence in one's ability to intervene).
Time frame: Baseline, 8 weeks, 16 weeks
Updated Illinois Rape Myth Acceptance Scale,
The Updated Illinois Rape Myth Acceptance Scale, is a 22-item instrument designed to measure contemporary, often subtle, rape-supportive beliefs. It updates the original 45-item scale to reflect modern language and attitudes, aiming to reduce social desirability bias, featuring a 5-point Likert scale (1 = Strongly Agree, 5 = Strongly Disagree). The higher the score is the worse score indicating that the participants holds negative rape myth scores.
Time frame: Baseline, 8 weeks, 16 weeks
Intent to Help Friends-Stranger Scale
Intent to Help Friends-Stranger Scale is a psychometric instrument designed to measure a bystander's intention to intervene in situations involving interpersonal violence (sexual assault, dating violence) depending on their relationship to the victim. The higher the score is the better score indicating participants are more willing to help a friend or stranger in a probably dangerous situation.
Time frame: Baseline, 8 weeks, 16 weeks
Alcohol Expectancies Regarding Sex, Aggression, and Sexual Vulnerability Questionnaire
The Alcohol Expectancies Regarding Sex, Aggression, and Sexual Vulnerability Questionnaire is used too assess three types of sex-related alcohol expectancies: sexual affect, sexual drive, and vulnerability to sexual coercion. A higher score is worse than a lower score.
Time frame: Baseline, 8 weeks, 16 weeks
Plan to share: Yes — The research team will retain and share aggregated quantitative and qualitative data (after all identifying information is redacted), if users commit to the following: (1) using the data only for research purposes and not to identify any individual participant; (2) securing the data using appropriate computer technology (for example, using a secure firewall-protected server to store datasets and transcriptions); and (3) destroying or returning the data after analyses are completed. If the researcher agrees to these stipulations, the PI will send him/her the data set prepared using Statistical Package for Social Sciences 29 and/or the de-identified transcriptions from focus groups. Research participants will be identified by number. All data, including focus group transcriptions, will not include identifying information from any participant. Any information that could potentially identify a participant will be removed from the data set.
Supporting information: Study protocol, Statistical analysis plan, Informed consent form
Time frame: The scientific data will be made available to other users no later than time of an associated publication or end of the performance period, whichever comes first and for how long data will be available.
Access criteria: Upon completion of the proposed study, we will work with the program officer to access how to share the data and will follow their direction.
Started Sep 2026 (actual). Primary completion is estimated for May 2027, 7 months after the start.
How these figures are worked out, and which studies are left out of them.
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
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University of New Hampshire