[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"labor-duration\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:labor-duration":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,49,80],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100644420","integrated-intrapartum-supportive-care-and-pushing-strategies-in-women-receiving-low-dose-epidural-analgesia-100644420",false,"NCT07663500","Integrated Intrapartum Supportive Care and Pushing Strategies in Women Receiving Low-Dose Epidural Analgesia","Integrated Intrapartum Supportive Care Combined With Different Pushing Strategies Among Women Receiving Low-Dose Epidural Analgesia: A Three-Arm Non-Randomized Quasi-Experimental Study","Inclusion Criteria:low-risk pregnant women aged 18 years or older with a singleton, term pregnancy (37-42 weeks), spontaneous labor onset, and planning to receive low-dose epidural analgesia.\n\nExclusion Criteria: Exclusion Criteria: multiple gestation, non-cephalic presentation, known major fetal anomalies, planned cesarean birth, contraindications to vaginal birth, contraindications to maternal mobility or epidural analgesia, or inability to provide informed consent.","FEMALE","18 Years",{"count":19,"type":20},159,"ESTIMATED","INTERVENTIONAL",[23],"NA","This prospective, three-arm, non-randomized quasi-experimental study aims to evaluate integrated intrapartum supportive care combined with different pushing strategies among women at 37-42 weeks of gestation who receive low-dose epidural analgesia. Participants receive integrated intrapartum supportive care combined with spontaneous pushing, integrated intrapartum supportive care combined with immediate pushing, or routine intrapartum care combined with immediate pushing. The primary outcomes are the durations of the first and second stages of labor. Secondary outcomes include mode of birth, obstetric interventions, maternal outcomes, and neonatal outcomes.",[26,27,28],"Labor, Obstetric","Epidural Analgesia, Obstetric","Labor Duration",[30,31,32,33,34,35],"Integrated intrapartum supportive care","Spontaneous pushing","Immediate pushing","Low-dose epidural analgesia","Maternal mobility","Labor progression","RECRUITING","2026-06-17",{"date":39,"type":40},"2026-06-23","ACTUAL",{"date":42,"type":40},"2025-06-10",{"date":44,"type":20},"2026-07-31",{"name":46,"class":47},"National Taipei University of Nursing and Health Sciences","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":21,"phases":59,"briefSummary":60,"conditions":61,"keywords":65,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":48},"100596965","the-moby-study-efficacy-of-birth-mobility-100596965","NCT07052331","The MOBY Study: Efficacy of Birth Mobility","The MOBY Study - Efficacy of Birth Mobility: Randomized Clinical Trial Investigating the Efficacy of Birth Mobility on Birth Outcomes in Primiparous Women With and Without a Birth Mobility System.","MOBY","Inclusion Criteria:\n\n* Age ≥ 18 years\n* German- or English-speaking\n* Able to provide written informed consent with capacity of judgment\n* Low-risk singleton pregnancy\n* Primiparous woman\n* Cephalic presentation\n* Gestational age at delivery ≥ 37 + 0 weeks\n\nExclusion Criteria:\n\n* Multiparous woman\n* Not capable of understanding instructions for use of the mobility system (intervention group)\n* Scheduled (elective) cesarean section\n* Contraindication to vaginal delivery\n* Multiple pregnancy\n* Breech presentation\n* Estimated fetal weight \\\u003C 10th percentile or \\> 90th percentile\n* Relevant fetal congenital abnormalities affecting neonatal adaptation\n* Pre-existing medical conditions significantly affecting mobility (e.g., orthopedic conditions, osteoporosis, multiple sclerosis, spinal cord injury)\n* Relevant intrapartum bleeding\n* Preeclampsia or HELLP syndrome",{"count":58,"type":20},714,[23],"This randomized clinical trial investigates whether and how maternal mobility during labor influences birth outcomes in primiparous women. The study compares standard obstetric care with care that includes a birth mobility system. The primary aim is to assess whether the system helps reduce secondary cesarean section rates. Secondary objectives include evaluation of labor progression, medication use, newborn health, and user satisfaction. Participation occurs during birth and includes the collection of routine clinical data and a short questionnaire afterward.",[28,62,63,64],"Cesarean Section Rate","Maternal Mobility","Healthy",[66,67,68,69],"Birth mobility","Maternal satisfaction","Labor and delivery","Neonatal outcomes","2025-12-16",{"date":72,"type":40},"2025-12-23",{"date":74,"type":40},"2025-07-25",{"date":76,"type":20},"2028-08",{"name":78,"class":79},"Vibwife AG","INDUSTRY",{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":4,"eligibilityCriteria":86,"healthyVolunteers":87,"sex":16,"minAge":88,"maxAge":89,"enrollmentInfo":90,"targetDuration":4,"studyType":21,"phases":92,"briefSummary":93,"conditions":94,"keywords":4,"overallStatus":95,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":4},"100597044","peanut-ball-during-the-first-stage-of-labor-100597044","NCT07053371","Peanut Ball During the First Stage of Labor","Effectiveness of Peanut Ball During the First Stage of Labor on Maternal and Neonatal Outcomes","Inclusion Criteria:\n\n* Low-risk primipara in active phase of labor, aged 20 -35 years with single living fetus in cephalic presentation and full-term pregnancy which lasts between 37-42 weeks\n\nExclusion Criteria:\n\n* Women with medical or obstetric complications were excluded from the study.",true,"20 Years","35 Years",{"count":91,"type":20},104,[23],"The current study aimed to assess the effectiveness of peanut ball during first stage of labor on maternal and neonatal outcomes.",[28],"NOT_YET_RECRUITING","2025-06-27",{"date":98,"type":40},"2025-07-08",{"date":100,"type":20},"2025-07",{"date":102,"type":20},"2026-08",{"name":104,"class":47},"Mansoura University"]