Sexual Assault

6

Review clinical trials related to Sexual Assault. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

uSafeUS+ App Pilot Testing

The purpose of this study is to test the feasibility and acceptability of an innovative mobile application (uSafeUS+) to reduce college student drinking and sexual assault (SA) risk in real time. Following an initial period of app development, this study will use a pilot 3-arm randomized controlled trial (N = 90; 30/arm) to examine the acceptability, feasibility, and initial evidence of efficacy of the novel, expanded uSafeUS+ app, relative to the existing SA-only focused uSafeUS app (already in use on 24 college campuses), and an assessment-only control condition. Specifically, the investigators aim to answer the following research questions: 1. Do students like the app (overall and specific features)? 2. How frequently do students use the app within the 1-month exposure period? 3. What barriers and facilitators impact app use? 4. Is there evidence of increased use of protective behaviors on drinking days and over time? 5. Is there evidence of decreased drinking (amount, frequency) or SA risk on drinking days and over time? Participants will complete: * A baseline assessment * A 1-month app exposure period with daily surveys about app use on the weekends * Follow-up surveys at 1- and 2-months post-intervention.

Participants needed: 90
Trial details
Age: 18-25Biological sex: AllType: InterventionalSponsor: University of FloridaUpdated: Jun 15, 2026Locations: 2
Eligibility criteria

Participants must be between the ages of 18 and 25 years old; [+5]

Unable or unwilling to provide informed consent

Status: Not yet recruiting

Evaluating a Digital Intervention to Improve Adolescent Condom Use and Communication

The purpose of this study is to test the effectiveness, likability, and implementation potential of PACT, an adapted digital program to teach non-heterosexual adolescent boys about sexual consent and condom negotiation in a randomized controlled trial over 9 months.

Participants needed: 300
Trial details
Age: 14-17Biological sex: AllType: InterventionalSponsor: North Carolina Agriculture & Technical State UniversityUpdated: Mar 30, 2026Locations: 1
Eligibility criteria

14-17 years old [+2]

younger than 14 [+3]

Status: Recruiting

The BEAR Program for Women With Trauma Who Have Suicidal Thoughts

The current study aims to test the feasibility of a new form of group therapy for women who have a history of interpersonal trauma and current suicidal ideation. The Building Empowerment and Resilience (BEAR) Therapeutic group has been adapted for women who have experienced trauma and have current suicidal ideation. It incorporates psychological skills, psychoeducation about trauma and gender-based violence, and physical self-defense training, all within a therapeutic process. It will be implemented with women who have experienced interpersonal trauma (physical, sexual, or emotional abuse/neglect) and experience various mental health difficulties, including suicidal ideation. We aim to assess the feasibility to recruit and implement the BEAR group. Our ultimate aim is to assess whether the program can effect self-efficacy and suicidal ideation.

Participants needed: 30
Trial details
Age: 18-75Biological sex: FemaleType: InterventionalSponsor: Stanford UniversityUpdated: Feb 20, 2026Locations: 1
Eligibility criteria

Women ages 18-75 [+2]

Active, significant substance abuse, which could interfere with participation [+6]

Status: Not yet recruiting

Improving HIV Prevention and Substance Use Post-Sexual Assault Services

The purpose of this study is to tailor existing sexual assault nurse examiner (SANE) services with same-day HIV prophylaxis and substance use screening, brief intervention, or referral using semi-structured adolescents and young adults (AYA) survivor and key informant interviews, and iterative co-design/pilot testing of adapted strategies with the youth working group (YWG), to optimize study mechanisms and outcome measures using cognitive interviews, analysis of community partner data, and recruitment and retention strategies with the youth working group (YWG) and community advisory board (CAB), to conduct a pilot randomized controlled trial with 40 AYA to test feasibility, acceptability, and initial efficacy compared to usual care, to evaluate recruitment, randomization, and follow-up strategies; adherence to intervention dose; retention benchmarks; and acceptability and to evaluate preliminary efficacy of outcome measures (uptake of post-assault HIV prevention and substance use treatment).

Participants needed: 90
Trial details
Age: 17-25Biological sex: AllType: InterventionalSponsor: The University of Texas Health Science Center, HoustonUpdated: Nov 5, 2025Locations: 1
Eligibility criteria

experienced a sexual assault within the last 72 hours [+2]

noticeably intoxicated or under the influence [+1]

Status: Recruiting

An Evaluation of an Online Sexual Assault Resistance Program (IDEA3)

The goal of this randomized trial is to test whether the Internet-Delivered Enhanced Assess, Acknowledge, Act (IDEA3) sexual assault resistance education intervention reduces sexual violence victimization in undergraduate women. Participants in the intervention group will be asked to attend four three-hour group sessions of a sexual assault resistance program called IDEA3 with a partner, as well as fill out a number of surveys. Participants in the control group will be asked to attend a one-hour consent workshop with a partner and fill out surveys. Researchers will compare sexual assault victimization between the groups in the one year following the intervention.

Participants needed: 1,920
Trial details
Age: 17-24Biological sex: AllType: InterventionalSponsor: University of Maryland, College ParkUpdated: Oct 21, 2025Locations: 6
Eligibility criteria

1st- and 2nd-year university students at one of the 4 sites [+4]

Status: Recruiting

Code of Respect (X-CoRe): Trial of a Multi-level Sexual Assault and Sexual Harassment Prevention Intervention for Active Duty Airmen

The purpose of this study is to examine the efficacy of Code of Respect (X-CoRe) multi-level sexual assault (SA) and harassment (SH) prevention program in improving psychosocial determinants (e.g., knowledge, skills, self-efficacy, attitudes) related to respectful/disrespectful relationships, to examine the efficacy of X-CoRe in reducing SA and sexual harassment SH victimization and to examine the efficacy of X-CoRe increasing bystander behavior and improving unit cohesion and mission readiness by decreasing secondary risk and harmful behaviors (e.g., alcohol misuse, intimate partner violence, suicide ideation). The study will be conducted at at Joint Base McGuire Dix-Lakehurst (JBMDL) located in Burlington County, New Jersey, and participants will be cluster-randomized at the level of the squadron to one of two conditions: the X-CoRe program or a control condition.

Participants needed: 1,200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: The University of Texas Health Science Center, HoustonUpdated: Jan 28, 2025Locations: 1
Eligibility criteria

Active Duty, stationed at JBMDL [+3]

being in service branches other than Air Force (e.g., Army or Navy) [+1]