[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100596965":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":23,"centralContacts":28,"locations":33,"responsibleParty":50,"collaborators":52,"id":57,"slug":58,"hasResults":59,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":63,"eligibilityCriteria":64,"healthyVolunteers":59,"sex":65,"minAge":66,"maxAge":18,"enrollmentInfo":67,"targetDuration":18,"studyType":70,"phases":71,"briefSummary":73,"conditions":74,"keywords":79,"overallStatus":35,"whyStopped":18,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":93},{"fullName":5,"class":6},"Vibwife AG","INDUSTRY",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Birth Mobility System","EXPERIMENTAL","Participants receive standard obstetric care and have access to a birth mobility system installed on the birthing bed. Use of the system is voluntary and guided by medical professionals. Participants view a video explaining the system's operation. Birth mobility data is collected passively.",[13],"Device: Birth Mobility System",{"label":15,"type":16,"description":17,"interventionNames":18},"Standard obstetric care","NO_INTERVENTION","Participants receive standard obstetric care using a conventional birthing bed. No access is given to the birth mobility system. Birth mobility data is collected passively.",null,[20],{"type":21,"name":9,"description":11,"armGroupLabels":22,"otherNames":18},"DEVICE",[9],[24],{"name":25,"affiliation":26,"role":27},"Prof. Dr. med. Leonhard Schäffer","Kantonsspital Baden","PRINCIPAL_INVESTIGATOR",[29],{"name":25,"role":30,"phone":31,"phoneExt":18,"email":32},"CONTACT","+41 56 486 35 07","leonhard.schaeffer@ksb.ch",[34],{"facility":26,"status":35,"city":36,"state":37,"zip":38,"country":39,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"RECRUITING","Baden","Canton of Aargau","5404","Switzerland","CH",{"type":42,"coordinates":43},"Point",[44,45],8.30592,47.47333,{"lat":45,"lon":44},[48,49],{"name":25,"role":30,"phone":31,"phoneExt":18,"email":32},{"name":25,"role":27,"phone":18,"phoneExt":18,"email":18},{"type":51,"investigatorFullName":18,"investigatorTitle":18,"investigatorAffiliation":18,"oldNameTitle":18,"oldOrganization":18},"SPONSOR",[53,55],{"name":26,"class":54},"OTHER",{"name":56,"class":54},"Fachhochschule Nordwestschweiz","100596965","the-moby-study-efficacy-of-birth-mobility-100596965",false,"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","FEMALE","18 Years",{"count":68,"type":69},714,"ESTIMATED","INTERVENTIONAL",[72],"NA","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.",[75,76,77,78],"Labor Duration","Cesarean Section Rate","Maternal Mobility","Healthy",[80,81,82,83],"Birth mobility","Maternal satisfaction","Labor and delivery","Neonatal outcomes","2025-12-16",{"date":86,"type":87},"2025-12-23","ACTUAL",{"date":89,"type":87},"2025-07-25",{"date":91,"type":69},"2028-08",{"name":5,"class":6},1]