[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"sexual-assault\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:sexual-assault":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,49,82,116,138,161],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100635827","usafeus-app-pilot-testing-100635827",false,"NCT07557745","uSafeUS+ App Pilot Testing","Expanding the uSafeUS Mobile App to Reduce Alcohol-Involved Sexual Assault on College Campuses","Inclusion Criteria:\n\n* Participants must be between the ages of 18 and 25 years old;\n* Currently enrolled as a residential undergraduate student at a participating university;\n* Intend to reside on or near (in the same town) campus over the two-month study period\n* Own a smartphone\u002Fmobile device;\n* Have consumed at least one alcoholic beverage per week or engaged in dating or social behaviors where alcohol is present at least once a week over the past 30 days;\n* Intend to drink or go out at the same frequency (at least weekly) over the two-month study period\n\nExclusion Criteria:\n\n* Unable or unwilling to provide informed consent",true,"ALL","18 Years","25 Years",{"count":21,"type":22},90,"ESTIMATED","INTERVENTIONAL",[25],"NA","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\u002Farm) 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.\n\nSpecifically, the investigators aim to answer the following research questions:\n\n1. Do students like the app (overall and specific features)?\n2. How frequently do students use the app within the 1-month exposure period?\n3. What barriers and facilitators impact app use?\n4. Is there evidence of increased use of protective behaviors on drinking days and over time?\n5. Is there evidence of decreased drinking (amount, frequency) or SA risk on drinking days and over time?\n\nParticipants will complete:\n\n* A baseline assessment\n* A 1-month app exposure period with daily surveys about app use on the weekends\n* Follow-up surveys at 1- and 2-months post-intervention.",[28,29],"Alcohol Consumption","Sexual Assault",[31,32,33,34,35],"Alcohol harm reduction","Sexual Assault Risk Reduction","Protective Behavioral Strategy Use","College students","MHealth","RECRUITING","2026-06-11",{"date":39,"type":40},"2026-06-15","ACTUAL",{"date":42,"type":40},"2026-05-11",{"date":44,"type":22},"2026-08-31",{"name":46,"class":47},"University of Florida","OTHER",2,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":16,"sex":17,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":23,"phases":59,"briefSummary":60,"conditions":61,"keywords":63,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":81},"100583625","evaluating-a-digital-intervention-to-improve-adolescent-condom-use-and-communication-100583625","NCT06878755","Evaluating a Digital Intervention to Improve Adolescent Condom Use and Communication","Inclusion Criteria:\n\n* 14-17 years old\n* lives in the U.S.\n* identifies as a queer teen guy or sexual minority male\n\nExclusion Criteria:\n\n* younger than 14\n* older than 17\n* does not live in U.S.\n* does not identify as a queer teen guy or sexual minority male","14 Years","17 Years",{"count":58,"type":22},300,[25],"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.",[62,29],"Condomless Sex",[64,65,66,67,68,69,70],"online intervention","digital health","sexual consent","condom use","condom negotiation","LGBTQ health","adolescents","NOT_YET_RECRUITING","2026-03-24",{"date":74,"type":40},"2026-03-30",{"date":76,"type":22},"2026-06",{"date":78,"type":22},"2028-01",{"name":80,"class":47},"North Carolina Agriculture & Technical State University",1,{"id":83,"slug":84,"hasResults":11,"nctId":85,"briefTitle":86,"officialTitle":87,"acronym":88,"eligibilityCriteria":89,"healthyVolunteers":11,"sex":90,"minAge":18,"maxAge":91,"enrollmentInfo":92,"targetDuration":4,"studyType":23,"phases":94,"briefSummary":95,"conditions":96,"keywords":102,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":107,"lastUpdatePostDateStruct":108,"startDateStruct":110,"completionDateStruct":112,"leadSponsor":114,"locationsCount":81},"100619593","the-bear-program-for-women-with-trauma-who-have-suicidal-thoughts-100619593","NCT07346638","The BEAR Program for Women With Trauma Who Have Suicidal Thoughts","A Pilot Study of the Building Empowerment and Resilience Program for Suicidal Ideation","BEAR-SI","Inclusion Criteria:\n\n* Women ages 18-75\n* History of physical, sexual, and\u002For sexual emotional violence, with subsequent interpersonal or psychological distress (e.g., depression or anxiety) related to this history.\n* Current suicidal thinking\n\nExclusion Criteria:\n\n* Active, significant substance abuse, which could interfere with participation\n* Significant medical conditions that would preclude safe participation in the study\n* No history of interpersonal trauma\n* Acute psychiatric instability\n* History of assaultive behavior or is judged to be a potential risk to assault others.\n* No current suicidal ideation or behaviors\n* Unable to commit to the group for 12 weeks in-person","FEMALE","75 Years",{"count":93,"type":22},30,[25],"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\u002Fneglect) 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.",[97,98,99,100,101,29],"Interpersonal Trauma","Depression","PTSD","Anxiety","Suicidal Ideations",[103,104,105,106],"interpersonal trauma","sexual assault","suicidal ideation","self-defense","2026-02-18",{"date":109,"type":40},"2026-02-20",{"date":111,"type":40},"2026-02-17",{"date":113,"type":22},"2028-08",{"name":115,"class":47},"Stanford University",{"id":117,"slug":118,"hasResults":11,"nctId":119,"briefTitle":120,"officialTitle":121,"acronym":4,"eligibilityCriteria":122,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":19,"enrollmentInfo":123,"targetDuration":4,"studyType":23,"phases":124,"briefSummary":125,"conditions":126,"keywords":4,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":129,"lastUpdatePostDateStruct":130,"startDateStruct":132,"completionDateStruct":134,"leadSponsor":136,"locationsCount":81},"100610244","improving-hiv-prevention-and-substance-use-post-sexual-assault-services-100610244","NCT07225062","Improving HIV Prevention and Substance Use Post-Sexual Assault Services","Improving HIV Prevention and Substance Use Post-Sexual Assault Services for Adolescents and Young Adults","Inclusion Criteria:\n\n* experienced a sexual assault within the last 72 hours\n* speak English\n* not planning to move out of the metro area during the study.\n\nExclusion Criteria:\n\n* noticeably intoxicated or under the influence\n* are overtly having severe, untreated mental illness symptoms",{"count":21,"type":22},[25],"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\u002Fpilot 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).",[127,128,29],"HIV Infections","Substance Use","2025-11-03",{"date":131,"type":40},"2025-11-05",{"date":133,"type":22},"2027-01-04",{"date":135,"type":22},"2027-06-30",{"name":137,"class":47},"The University of Texas Health Science Center, Houston",{"id":139,"slug":140,"hasResults":11,"nctId":141,"briefTitle":142,"officialTitle":143,"acronym":144,"eligibilityCriteria":145,"healthyVolunteers":16,"sex":17,"minAge":56,"maxAge":146,"enrollmentInfo":147,"targetDuration":4,"studyType":23,"phases":149,"briefSummary":150,"conditions":151,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":152,"lastUpdatePostDateStruct":153,"startDateStruct":155,"completionDateStruct":157,"leadSponsor":159,"locationsCount":5},"100520583","an-evaluation-of-an-online-sexual-assault-resistance-program-idea3-100520583","NCT06058455","An Evaluation of an Online Sexual Assault Resistance Program (IDEA3)","A Randomized Controlled Trial of the Efficacy of IDEA3 - An Evidence-based Sexual Assault Resistance Intervention for Undergraduate Women Adapted for Internet Delivery","IDEA3","Inclusion Criteria:\n\n* 1st- and 2nd-year university students at one of the 4 sites\n* female-identifying students\n* students between ages of 17-24\n* able to attend one of the scheduled program groups\n* able and willing to be matched with another eligible student\n\nExclusion Criteria:\n\n\\- None","24 Years",{"count":148,"type":22},1920,[25],"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.\n\nParticipants 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.\n\nResearchers will compare sexual assault victimization between the groups in the one year following the intervention.",[29],"2025-10-18",{"date":154,"type":40},"2025-10-21",{"date":156,"type":40},"2023-10-02",{"date":158,"type":22},"2027-12-31",{"name":160,"class":47},"University of Maryland, College Park",{"id":162,"slug":163,"hasResults":11,"nctId":164,"briefTitle":165,"officialTitle":166,"acronym":4,"eligibilityCriteria":167,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":168,"targetDuration":4,"studyType":23,"phases":170,"briefSummary":171,"conditions":172,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":174,"lastUpdatePostDateStruct":175,"startDateStruct":177,"completionDateStruct":179,"leadSponsor":181,"locationsCount":81},"100523849","code-of-respect-x-core-trial-of-a-multi-level-sexual-assault-and-sexual-harassment-prevention-intervention-for-active-duty-airmen-100523849","NCT06101056","Code of Respect (X-CoRe): Trial of a Multi-level Sexual Assault and Sexual Harassment Prevention Intervention for Active Duty Airmen","Code of Respect (X-CoRe): a Randomized Controlled Trial of a Multi-level Sexual Assault and Sexual Harassment Prevention Intervention for Active Duty Airmen","Inclusion Criteria:\n\n* Active Duty, stationed at JBMDL\n* assigned to one of the 26 Air Force squadrons within the three Air Force Wings at JBMDL (87 Air Base Wing (ABW), 305 Air Mobility Wing (ABM), and 621 Contingency Response Wing (CRW))\n* English speaking\n* access to an electronic device with internet capabilities\n\nExclusion Criteria:\n\n* being in service branches other than Air Force (e.g., Army or Navy)\n* Airmen not ranked E1-E4 at JBMDL",{"count":169,"type":22},1200,[25],"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\u002Fdisrespectful 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.",[29,173],"Sexual Harassment","2025-01-24",{"date":176,"type":40},"2025-01-28",{"date":178,"type":40},"2024-12-17",{"date":180,"type":22},"2027-05-31",{"name":137,"class":47}]