[{"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,3,0,[8,46,76],{"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":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":17,"sex":18,"minAge":54,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":24,"phases":57,"briefSummary":58,"conditions":59,"keywords":62,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":75},"100533234","optimizing-the-floreciendo-sexual-and-reproductive-health-workshop-for-latina-teens-and-female-caregivers-a-pilot-100533234","NCT06223165","Optimizing the Floreciendo Sexual and Reproductive Health Workshop for Latina Teens and Female Caregivers: A Pilot","Evidence-based Sexual and Reproductive Health Intervention Using a Multiphase Optimization Strategy","Floreciendo","Inclusion criteria for teens:\n\n1. Identify as Latina\n2. Be 14-18 years old\n3. Speak English and\u002For Spanish\n4. Be available and have a female caregiver who is available for the workshop and research activities.\n5. Be living with or in daily contact with the female caregiver.\n\nInclusion criteria for female caregivers:\n\n1. Be the mother or a female caregiver (e.g., aunt, sister, grandmother) of a Latina teen (aged 14-18 years old)\n2. Be 19 years old or older\n3. Speak English and\u002For Spanish\n4. Be available and have a teen who is available for the workshop and research activities.\n5. Be living with or in daily contact with the Latina teen.\n\nLatina teens and female caregivers must agree to participate as a dyad, and teens' refusal will supersede parental consent.\n\nExclusion Criteria:\n\nTeens and caregivers will be excluded if they are unable to understand the consent\u002Fassent process and provide informed consent\u002Fassent or if they already received the intervention in a previous phase of the research. Teens may or may not be sexually active; this will not be an exclusion criterium. Information about teens' sexual activity will not be shared with caregivers to reduce consent\u002Fassent barriers. If there is more than one eligible adolescent in the family, we will randomly select one to maintain independent observations. Teens or caregivers who become pregnant during the study may continue to participate. Prisoners will be excluded.","14 Years",{"count":56,"type":23},184,[26],"Floreciendo is a sexual and reproductive health workshop for Latina teens (ages 14-18 years) and their female caregivers (e.g., mothers, sisters, grandmothers). This study involves conducting a pilot optimization trial of Floreciendo using the multiphase optimization strategy (MOST) framework. The feasibility of using a 2 x 2 x 2 factorial trial design and the acceptability of the intervention components of Floreciendo will be examined. Effectiveness and implementation outcomes will be explored. This work will be conducted in partnership with community-based organizations in the Chicagoland area.",[60,31,61],"Sexual Risk Behavior","Unplanned Pregnancy",[63,64,65],"Sexual and reproductive health","Latina teens","Mother-daughter intervention","2025-02-25",{"date":68,"type":37},"2025-02-27",{"date":70,"type":37},"2024-03-09",{"date":72,"type":23},"2026-08",{"name":74,"class":44},"University of Illinois at Chicago",4,{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":80,"acronym":81,"eligibilityCriteria":82,"healthyVolunteers":17,"sex":83,"minAge":54,"maxAge":19,"enrollmentInfo":84,"targetDuration":4,"studyType":24,"phases":86,"briefSummary":87,"conditions":88,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"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",{"count":85,"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.",[89,90,91,31],"Health Behavior","Health Care Utilization","Unprotected Sex","2023-11-17",{"date":94,"type":37},"2023-11-21",{"date":96,"type":37},"2023-06-12",{"date":98,"type":23},"2026-09-29",{"name":100,"class":44},"Child Trends"]