[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"sexually-transmitted-infections\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:sexually-transmitted-infections":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,46],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100497164","gathering-online-for-dialogue-and-discussion-to-enhance-social-support-100497164",false,"NCT05753683","Gathering Online for Dialogue and Discussion to Enhance Social Support","GODDESS (Gathering Online for Dialogue and Discussion to Enhance Social Support): Engaging Young African American Women in a Virtual Group App to Address Alcohol Misuse, Sexual Risk, and Pre-exposure Prophylaxis (PrEP) in North Carolina (NC)","GODDESS","Selected Inclusion Criteria:\n\n* identify as Black\u002FAfrican American\n* identify as female\n* be between 18 and 30 years old\n* recent substance use\n* HIV negative and not currently on PrEP\n* have an Android or iOS-based smartphone\n\nSelected Exclusion Criteria:\n\n* test positive for HIV\n* participated in the previous study activities of the current study or previous related studies",true,"ALL","18 Years","30 Years",{"count":22,"type":23},500,"ESTIMATED","INTERVENTIONAL",[26],"NA","The goal of this trial is to test a modified mobile health intervention (with a group component) relative to a mobile health intervention in a two-arm randomized trial with up to 500 young women who are human immunodeficiency virus (HIV)-negative and who misuse alcohol.\n\nThe expected outcomes are to: (1) determine the efficacy of the virtual group component in reducing alcohol use and sexual risk and increasing pre-exposure prophylaxis (PrEP) utilization; and (2) understand selected outcomes for implementation.\n\nParticipants will be randomized to receive either the mHealth app or the mHealth app plus the group component, and followed up at 3- and 6-months post-enrollment.",[29,30,31,32],"Alcohol Misuse","HIV","Sexually Transmitted Infections","Pre-exposure Prophylaxis","RECRUITING","2026-05-15",{"date":36,"type":37},"2026-05-19","ACTUAL",{"date":39,"type":37},"2025-04-07",{"date":41,"type":23},"2027-11",{"name":43,"class":44},"RTI International","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":17,"sex":53,"minAge":54,"maxAge":19,"enrollmentInfo":55,"targetDuration":4,"studyType":24,"phases":57,"briefSummary":58,"conditions":59,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":45},"100519442","evaluation-of-the-safespace-app-intervention-100519442","NCT06043596","Evaluation of the SafeSpace App Intervention","SafeSpace","Inclusion Criteria:\n\n* Participants must be assigned female or intersex at birth\n* Participants must be youth in the U.S. (14-18 years old)\n* Participants must have daily access to an iPhone\n\nExclusion Criteria:\n\n\\- Participants must not be currently pregnant or currently trying to become pregnant\n\nOther Criteria:\n\n\\- The study's priority\u002Fpreference population is for Black and\u002For Latine youth, LGBTQ+ youth, youth from geographic areas with high teen birth rates, and youth living in rural areas.","FEMALE","14 Years",{"count":56,"type":23},1000,[26],"The goal of this study is to evaluate the impact of SafeSpace Sexual Health App, an innovative sexual health promotion program focused on reducing sexual risk factors and promoting sexual and reproductive health and wellbeing among young people assigned female or intersex at birth, particularly Black and\u002For Latine youth, LGBTQ+ youth, youth in states with high teen birth rates and youth who live in rural communities. This study utilizes a two-arm randomized control trial design to measure impacts of receiving the SafeSpace Sexual Health program compared to receiving a similar-length control app program, SafeSpace General Health that focuses on general health.\n\nThe investigators will ask participants to:\n\n* Keep the SafeSpace app downloaded to their device and visit the app regularly over the course of 10 weeks.\n* Provide contact information.\n* Receive and open app push notifications for 10 weeks (up to 3 per week).\n* Complete 3 online surveys over a year: baseline, short-term follow-up (10 weeks after baseline), and long-term follow up (9 months after short-term follow-up).\n* Receive occasional text messages from the study team.",[60,61,62,31],"Health Behavior","Health Care Utilization","Unprotected Sex","2023-11-17",{"date":65,"type":37},"2023-11-21",{"date":67,"type":37},"2023-06-12",{"date":69,"type":23},"2026-09-29",{"name":71,"class":44},"Child Trends"]