[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"reproductive-behavior\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:reproductive-behavior":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,46,74,113,141,169,191],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100627625","vasectomy-right-for-me-decision-support-tool-100627625",false,"NCT07451067","\"Vasectomy: Right for Me?\" Decision Support Tool","Addressing Factors Related to Disparities in Vasectomy","Inclusion Criteria:\n\n* Are assigned male at birth\n* 21-55 years of age\n* Comfortable reading in English or Spanish\n* Live in the United States\n* Are considering vasectomy\n* Have not had a vasectomy\n\nExclusion Criteria:\n\n* Are not assigned male at birth\n* Are less than 21 or more than 55 years of age\n* Is not comfortable reading English nor Spanish\n* Do not live in the United States\n* Are not considering vasectomy\n* Have had a vasectomy\n* Once a racial or economic sub-group recruitment number has been reached, no other subjects fitting that ethnicity or income group will be enrolled.","MALE","21 Years","55 Years",{"count":20,"type":21},750,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this trial is to learn if a web-based decision aid designed to provide evidence-based information about vasectomy and other birth control options helps improve users' decision-making about birth control. The main questions it aims to answer are:\n\n* Do people who use the decision aid have better knowledge about vasectomy?\n* Do people who use the decision aid have lower conflict with their decision?\n\nParticipants will:\n\n* Use the decision aid (if they are assigned to the intervention arm).\n* Answer survey questions about their knowledge, decision-making, interest in vasectomy, and healthcare navigation experiences.",[27,28,29,30],"Vasectomy","Contraception","Contraception Behavior","Reproductive Behavior",[27,32],"Decision aid","RECRUITING","2026-06-29",{"date":36,"type":37},"2026-07-01","ACTUAL",{"date":39,"type":37},"2026-06-20",{"date":41,"type":21},"2027-08",{"name":43,"class":44},"University of Pittsburgh","OTHER",2,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":53,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":22,"phases":58,"briefSummary":59,"conditions":60,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":73},"100634473","the-reach-out-trial-100634473","NCT07540143","The REACH-OUT Trial","A Technology-based, Primary Care Strategy to Optimize Blood Pressure Before Pregnancy: The REACH-OUT Trial","Inclusion Criteria:\n\n* biologically female\n* age 18-44\n* English or Spanish-speaking\n* prescribed an antiHTN\n* have a systolic BP \\>140 or diastolic BP\\>90 at their index visit\n* have access to the internet\n\nExclusion Criteria:\n\n* not pregnant or within 3 months postpartum\n* severe, uncorrectable vision, hearing, or cognitive impairment that would preclude study consent or participation","FEMALE","18 Years","44 Years",{"count":57,"type":21},350,[24],"Test the effectiveness of a technology-enabled strategy to optimize blood pressure among reproductive-aged women with hypertension receiving care in Federally Qualified Health Centers.",[61,30,62,63],"Hypertension","Primary Health Care","Electronic Health Record","2026-06-18",{"date":66,"type":37},"2026-06-22",{"date":68,"type":37},"2026-06-16",{"date":70,"type":21},"2030-06-30",{"name":72,"class":44},"Northwestern University",1,{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":4,"eligibilityCriteria":80,"healthyVolunteers":81,"sex":82,"minAge":54,"maxAge":4,"enrollmentInfo":83,"targetDuration":4,"studyType":85,"phases":4,"briefSummary":86,"conditions":87,"keywords":91,"overallStatus":103,"whyStopped":4,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":73},"100635380","womens-reproductive-choices-and-mental-health-during-pregnancy-and-after-birth-in-wartime-ukraine-100635380","NCT07551934","Women's Reproductive Choices and Mental Health During Pregnancy and After Birth in Wartime Ukraine","Integrative Model of Factors Influencing Reproductive Behavior and Perinatal Mental Health of Women Amidst War","Inclusion Criteria:\n\n* able and willing to provide informed consent;\n* aged 18 years or older.\n\nExclusion Criteria:\n\n* younger than 18 years;\n* unable to provide informed consent;\n* do not have sufficient language proficiency to complete the study procedures;\n* at the time of recruitment, they have an acute medical or psychological condition that would make participation unsafe, inappropriate, or unduly burdensome (e.g., obstetric emergencies, immediate postoperative or critical care status, or severe acute distress requiring urgent clinical care);\n* participation or the handling of personal data could reasonably pose a risk to the safety of the participant or their family.",true,"ALL",{"count":84,"type":21},328,"OBSERVATIONAL","The goal of this observational study is to learn how war affects reproductive decisions and perinatal mental health in Ukrainian women.\n\nThe main questions it aims to answer are: (1) how are wartime stress and trauma related to women's decisions about pregnancy and childbirth?; (2) what mental health symptoms and psychological difficulties are experienced during the perinatal period under wartime conditions? (3) which demographic, obstetric, and psychological factors are linked to poorer mental health and childbirth experiences?\n\nResearchers will survey at least 300 women.\n\nParticipants will: (1) complete questionnaires about their mental health and psychological well-being; (2) answer questions about their reproductive choices, pregnancy, and\u002For childbirth experiences; (3) report on the impact of war, social support, maternal care, and postpartum trauma; (4) provide demographic and obstetric information.\n\nThe findings will be used to develop an evidence-based model of the factors influencing reproductive behavior and perinatal mental health during war.",[88,30,89,90],"Perinatal Mental Health","Women","Cohort Studies",[92,93,94,95,96,97,98,99,100,101,102],"perinatal psychology","mental health","reproductive behavior","psychological trauma","PTSD","CB-PTSD","postpartum depression","pregnancy","sexual health","Ukraine","war-affected population","NOT_YET_RECRUITING","2026-05-04",{"date":106,"type":37},"2026-05-08",{"date":108,"type":21},"2026-06",{"date":110,"type":21},"2028-11",{"name":112,"class":44},"Taras Shevchenko National University of Kyiv",{"id":114,"slug":115,"hasResults":11,"nctId":116,"briefTitle":117,"officialTitle":118,"acronym":4,"eligibilityCriteria":119,"healthyVolunteers":11,"sex":53,"minAge":54,"maxAge":120,"enrollmentInfo":121,"targetDuration":4,"studyType":22,"phases":123,"briefSummary":124,"conditions":125,"keywords":126,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":132,"lastUpdatePostDateStruct":133,"startDateStruct":135,"completionDateStruct":137,"leadSponsor":139,"locationsCount":73},"100563366","the-impact-of-vaginal-washing-on-cervical-inflammation-100563366","NCT06615232","The Impact of Vaginal Washing on Cervical Inflammation","The Impact of Vaginal Washing on Cervical Inflammation: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Reports vaginal washing beyond the introitus in the past week\n* Female, aged 18-50\n* Presence of a cervix\n* Informed consent obtained and form signed\n* HIV-seronegative\n* Non-pregnant (urine β-hCG negative)\n* Willing to abstain from sex for 14 days after biopsy\n* Post-menarche and pre-menopause\n\nExclusion Criteria:\n\n* \\\u003C3 months postpartum or current breastfeeding\n* Current menstruation (can enroll after menses)\n* History of bleeding disorder\n* Visible cervical abnormality requiring evaluation\n* Medical contraindication to study protocol\n* Visible cervicovaginal ulcers or lesions\n* Positive test for gonorrhea, chlamydia, trichomonas, or wet preparation and examination findings indicating vulvovaginal candidiasis","50 Years",{"count":122,"type":21},122,[24],"Vaginal washing is a common practice that many women perceive as hygienic. However, vaginal washing has been linked to adverse reproductive health outcomes including increased HIV acquisition risk. The mechanism linking vaginal washing to HIV risk remains unknown, but may be related to increased inflammation caused by intravaginal washing practices. The primary objective of this study is to test the hypothesis that a vaginal washing cessation intervention will reduce concentrations of soluble inflammatory mediators in cervicovaginal fluid and total immune cells in mucosal tissue, reduce cervical epithelial disruption, and increase concentrations of protective vaginal Lactobacillus spp. compared to control.",[30],[127,128,129,130,131],"sex work","hiv","vaginal washing","cervicovaginal inflammation","mucosal barrier disruption","2026-04-28",{"date":134,"type":37},"2026-05-05",{"date":136,"type":37},"2025-05-16",{"date":138,"type":21},"2029-06",{"name":140,"class":44},"University of Washington",{"id":142,"slug":143,"hasResults":11,"nctId":144,"briefTitle":145,"officialTitle":146,"acronym":4,"eligibilityCriteria":147,"healthyVolunteers":81,"sex":53,"minAge":17,"maxAge":148,"enrollmentInfo":149,"targetDuration":4,"studyType":22,"phases":151,"briefSummary":152,"conditions":153,"keywords":154,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":160,"lastUpdatePostDateStruct":161,"startDateStruct":163,"completionDateStruct":165,"leadSponsor":167,"locationsCount":73},"100538896","patient-centered-information-on-permanent-contraception-100538896","NCT06296797","Patient-centered Information on Permanent Contraception","Disseminating PCOR Findings to Reduce Racial Disparities in Surgical Sterilization","Inclusion Criteria:\n\n* Self-reported fertility\n* Have a strong desire to avoid future pregnancy\n* Speak English or Spanish\n\nExclusion Criteria:\n\n* Current pregnancy\n* The inability to speak English or Spanish\n* Prior tubal sterilization or \"Essure\" procedure\n* Menopause\n* Infertility\n* Hysterectomy","45 Years",{"count":150,"type":21},650,[24],"The goal of this study is to understand whether providing information to women with a strong desire to avoid future pregnancy about how tubal sterilization compares to long-acting reversible contraceptives improves perceived access to available contraceptives.\n\nParticipants will:\n\n* Complete a baseline survey\n* Receive access to web-based educational resources\n* Complete a brief follow up survey immediately after exploring these web-based resources\n* Complete a follow-up survey 3 months after enrolling\n\nThe investigators will compare outcomes among participants provided with access to a new website (intervention) summarizing recent patient-centered outcomes research (PCOR) comparing interval laparoscopic tubal sterilization and long-acting reversible contraception (LARC) to control participants provided with access to the existing Planned Parenthood website on tubal sterilization.",[28,30,29],[155,156,157,158,159],"tubal sterilization","permanent contraception","intrauterine device","contraceptive implant","vasectomy","2026-01-22",{"date":162,"type":37},"2026-01-26",{"date":164,"type":37},"2024-04-01",{"date":166,"type":21},"2026-08-01",{"name":168,"class":44},"University of California, San Francisco",{"id":170,"slug":171,"hasResults":11,"nctId":172,"briefTitle":173,"officialTitle":174,"acronym":175,"eligibilityCriteria":176,"healthyVolunteers":11,"sex":53,"minAge":54,"maxAge":55,"enrollmentInfo":177,"targetDuration":4,"studyType":22,"phases":179,"briefSummary":180,"conditions":181,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":183,"lastUpdatePostDateStruct":184,"startDateStruct":186,"completionDateStruct":188,"leadSponsor":190,"locationsCount":73},"100437484","promoting-preconception-care-and-diabetes-self-management-among-reproductive-aged-women-with-diabetes-100437484","NCT04976881","Promoting Preconception Care and Diabetes Self-Management Among Reproductive-Aged Women With Diabetes","Promoting Preconception Care and Diabetes Self-Management Among Reproductive-Aged Women With Diabetes: The PREPARED Trial","PREPARED","Inclusion Criteria:\n\n* female\n* age 18-44\n* English or Spanish-speaking\n* have a chart diagnosis of type 2 diabetes\n* not currently pregnant\n* not infecund, sterilized, or in a monogamous relationship with a sterilized partner\n* have a private cell phone with text messaging capability.\n\nExclusion Criteria:\n\n* severe, uncorrectable vision, hearing, or cognitive impairments that would preclude study consent or participation",{"count":178,"type":21},840,[24],"This study is being done to investigate strategies that may improve patient's knowledge of type 2 diabetes during reproductive age and improve knowledge and engagement in self-care activities.",[182,63,62,30],"Diabetes Mellitus, Type 2","2025-11-14",{"date":185,"type":37},"2025-11-18",{"date":187,"type":37},"2022-05-06",{"date":189,"type":21},"2026-05",{"name":72,"class":44},{"id":192,"slug":193,"hasResults":11,"nctId":194,"briefTitle":195,"officialTitle":196,"acronym":197,"eligibilityCriteria":198,"healthyVolunteers":81,"sex":53,"minAge":199,"maxAge":200,"enrollmentInfo":201,"targetDuration":4,"studyType":22,"phases":203,"briefSummary":204,"conditions":205,"keywords":4,"overallStatus":103,"whyStopped":4,"lastUpdateSubmitDate":207,"lastUpdatePostDateStruct":208,"startDateStruct":210,"completionDateStruct":212,"leadSponsor":214,"locationsCount":73},"100362119","project-for-reproductive-equity-through-volunteers-and-entrepreneurship-networks-and-technology-100362119","NCT03995043","Project for Reproductive Equity Through Volunteers and Entrepreneurship, Networks and Technology","Project for Reproductive Equity Through Volunteers and Entrepreneurship, Networks and Technology: The PREVENT Project Protocol","PREVENT","Inclusion Criteria:\n\n* Women 15-19 years of age\n* Reside within the study area for the duration of the study\n* Have a personal mobile phone and be willing to provide the phone number to the researchers to receive the intervention messages\n* Report being SMS literate (ie. able to read text messages in English or Swahili)\n* Be able and willing to return for follow-up after 12 months\n* Be able and willing to give written informed consent for enrollment in the study\n\nExclusion Criteria:\n\n* Be pregnant or planning pregnancy within 12 months (assessed when obtaining consent using HCG (human chorionic gonadotropin) urine dipstick).\n* Participation in another study or intervention that may affect the outcome of this study\n* Already utilizing a long-term form of contraception such as intra-uterine device, or implantable or inject-able contraception\n* Having a non-medical condition detected through screening that hinders study participation such as developmental or cognitive delay","15 Years","19 Years",{"count":202,"type":21},198,[24],"The PREVENT Project is a multifaceted, adolescent friendly, culturally competent program aimed to address the issues surrounding unplanned pregnancies and lack of access and uptake of contraceptive services among adolescent girls. The intervention uses a mobile platform that provides educational SMS (Short Message Service) messaging, interactive voice response, and connects adolescent girls to community based AFSRH (Adolescent Friendly Sexual Reproductive Health) counselling services, as well as discreet contraceptive access points headed by female entrepreneurs. The program will be piloted for 12 months in various wards and villages in rural and urban Kilimanjaro, Tanzania.The acceptability and practicality of the intervention will be assessed using mixed methods. Questionnaires and focus groups will be conducted with the study participants, as well as the medical and non-medical volunteers at the start and end of the pilot. The study will be heavily supported by all-female non-medical social entrepreneurs and sexual reproductive health community mentors (volunteers), and, all-female medical reproductive health team. Recruitment will also take place in hair saloons (local hair braiding and styling establishments) and other female run business such as tailors and female clothing stores that have enlisted to become contraceptive access points in the study. There will be 2 intervention groups, control and case group. Both groups will receive educational SMS (text) messages on SRH (Sexual Reproductive Health) and access individually tailored educational resources through interactive voice response (IVR) services\u002Fsystem via PREVENT mobile platform. In addition to personal support to be able to contact with a SRH community peer mentor in the community for AFSRH counselling and support. The case group will then have access to contraception provided with detailed and discreet information on accessing PREVENT contraceptive access points in all communities included in the study.",[28,206,30],"Pregnancy Related","2025-03-17",{"date":209,"type":37},"2025-03-20",{"date":211,"type":21},"2026-12",{"date":213,"type":21},"2028-06-01",{"name":215,"class":44},"Dr. Karen Yeates"]