Trial · NCT07888153
Study of Cross-Cutting E-Health Prevention Approaches
NCT07888153, Phase 2, Recruiting, University of New Hampshire
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Study of Cross-Cutting E-Health Prevention Approaches. Trials, record NCT07888153. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07888153
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Study of Cross-Cutting E-Health Prevention Approaches
- NCT number
- NCT07888153
- Status
- Recruiting
- Phases
- Phase 2
- Enrollment
- 350 participants, estimated
- Lead sponsor
- University of New Hampshire
- Conditions
- Alcohol Misuse Prevention, Sexual Violence Prevention
- Interventions
- Cross Cutting e-health Prevention Program Individual Interventions
- First posted
- 2026-10-22
- Last updated
- 2026-10-22
Source ClinicalTrials.gov
Registered outcomes11
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Sexual Experiences Survey-Short Form Victimization | Baseline, 8 weeks, 16 weeks | 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. |
| Primary | Sexual Experiences Survey-Short Form Perpetration | Baseline, 8 weeks, 16 weeks | 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. |
| Primary | Alcohol Use Disorders Identification Test-Concise | Baseline, 8 weeks, 16 weeks | 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. |
| Primary | Drinking Behavior Questionnaire | Baseline, 8 weeks, 16 weeks | 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. |
| Secondary | Bystander Attitudes Scale Revised | Baseline, 8 weeks, 16 weeks | 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. |
| Secondary | Barriers to Sexual Assault Bystander Intervention Scale | Baseline, 8 weeks, 16 weeks | 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. |
| Secondary | Social Self-identification Scale | 8 weeks, 16 weeks | 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. |
| Secondary | Bystander Efficacy Scale | Baseline, 8 weeks, 16 weeks | 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). |
| Secondary | Updated Illinois Rape Myth Acceptance Scale, | Baseline, 8 weeks, 16 weeks | 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. |
| Secondary | Intent to Help Friends-Stranger Scale | Baseline, 8 weeks, 16 weeks | 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. |
1 to 10 of 11Source ClinicalTrials.gov
See all 11 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers15
The papers the trial lists on ClinicalTrials.gov.
Grants1
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years |
|---|---|---|---|---|---|
| R15AA031809 | A pilot study of cross-cutting e-health prevention approaches to address campus sexual assault and alcohol misuse | POTTER, SHARYN J | UNIVERSITY OF NEW HAMPSHIRE | NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM | 2025 |
Source NIH RePORTER
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07888153
GET https://conductscience.org/api/trials/v1/NCT07888153/registered