[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"maternal-satisfaction\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:maternal-satisfaction":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,41,73],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100624805","impact-of-patient-choice-for-epidural-potency-on-maternal-satisfaction-100624805",false,"NCT07414407","Impact of Patient Choice for Epidural Potency on Maternal Satisfaction","Inclusion Criteria:\n\n* Planned vaginal delivery\n* Patient requesting epidural labor analgesia\n* Gestational age \\>34 weeks\n\nExclusion Criteria:\n\n* Any contraindication to neuraxial block\n* History of chronic pain, anxiety or depression\n* Intolerance or allergy to local anesthetic or opioids\n* Cesarean delivery within 2 hours of epidural initiation","FEMALE","18 Years","50 Years",{"count":19,"type":20},150,"ESTIMATED","INTERVENTIONAL",[23],"NA","This clinical trial will compare two different approaches to epidural analgesia during labor to see which approach leads to higher patient satisfaction after delivery.\n\nPrimary aim: determine whether one approach produces greater postpartum maternal satisfaction.\n\nSecondary aims: compare pain control and side effects.\n\nParticipants are people in labor who receive epidural analgesia. They will receive routine clinical epidural care and complete brief, in-hospital questionnaires about pain and satisfaction.\n\nAll care is provided by the clinical team and safety practices remain unchanged.",[26,27],"Epidural Analgesia, Obstetric","Maternal Satisfaction","NOT_YET_RECRUITING","2026-02-10",{"date":31,"type":32},"2026-02-17","ACTUAL",{"date":34,"type":20},"2026-04-01",{"date":36,"type":20},"2030-12-31",{"name":38,"class":39},"Stanford University","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":48,"sex":15,"minAge":16,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":21,"phases":52,"briefSummary":53,"conditions":54,"keywords":61,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":40},"100614469","effect-of-a-respectful-maternity-care-based-action-plan-in-postpartum-care-on-maternal-and-neonatal-outcomes-100614469","NCT07280000","Effect of a Respectful Maternity Care-Based Action Plan in Postpartum Care on Maternal and Neonatal Outcomes","The Effect of the Action Plan Developed Within the Framework of Respectful Maternity Care in Postpartum Care on Maternal and Neonatal Outcomes","Inclusion Criteria:\n\n* Postpartum women aged 18 years and older\n* Gave birth at 37-42 gestational weeks (vaginal or cesarean)\n* Have a single, healthy newborn\n* No chronic medical conditions\n* No history of high-risk pregnancy or fetal complications\n* No communication barriers (e.g., visual or hearing impairment)\n* Able to speak and understand Turkish\n* Literate and able to read and write in Turkish\n\nExclusion Criteria:\n\n* Development of maternal or neonatal complications during the postpartum follow-up period\n* Inability to reach the mother at the 8-week postpartum follow-up",true,"49 Years",{"count":51,"type":20},500,[23],"This study will examine whether a Respectful Maternity Care-based action plan can improve the quality of postpartum care and maternal and newborn outcomes. Nurses and midwives will receive a three-day interactive training about respectful, evidence-based postpartum care. After training, a unit-level action plan will be implemented, including supportive visits, educational materials, and feedback meetings. Women receiving routine postpartum care before the intervention will be compared with women receiving care after implementation. Outcomes will include respectful maternity care experiences, maternal satisfaction, exclusive breastfeeding at 6-8 weeks, maternal mental health, mother-infant bonding, and postpartum complications. The goal of this study is to promote respectful, high-quality postpartum care and improve the health and well-being of mothers and newborns.",[55,56,57,58,59,60,27],"Postpartum Care","Maternal Health Care","Newborn Health","Postpartum Depression (PPD)","Breastfeeding","Quality of Care",[62,55,63,57],"Respectful Maternity Care","Maternal Health","2025-12-01",{"date":66,"type":32},"2025-12-12",{"date":68,"type":20},"2025-12-10",{"date":70,"type":20},"2026-12-01",{"name":72,"class":39},"ilayda sel",{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":79,"eligibilityCriteria":80,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":81,"targetDuration":4,"studyType":21,"phases":83,"briefSummary":84,"conditions":85,"keywords":4,"overallStatus":91,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":40},"100592961","pushing-using-real-time-sonographic-ultrasound-education-100592961","NCT07000240","Pushing Using Real-time Sonographic Ultrasound Education","Pushing Using Real-time Sonographic Ultrasound Education (PURSUE)","PURSUE","Inclusion Criteria:\n\n1. Nulliparous women in their second trimester (approximately 14-28 weeks of gestation).\n2. Willingness to participate in the preparation training program on pushing techniques.\n3. Singleton pregnancy.\n4. Age 18 years or older.\n5. Ability to understand and provide informed consent in Italian.\n6. Plan to deliver at the Fondazione Policlinico Agostino Gemelli IRCCS.\n\nExclusion Criteria:\n\n1. Multifetal (e.g., twins, triplets) pregnancies.\n2. Known obstetric complications or conditions that contraindicate a vaginal delivery (e.g., placenta previa).\n3. Medical or psychiatric conditions that would prevent participation in the educational program or adherence to study protocols.\n4. History of pelvic floor surgery or severe pelvic floor dysfunction that might affect participation or outcomes.\n5. Inability to understand study requirements or provide informed consent.\n6. Participants already enrolled in conflicting clinical trials or interventions that could influence the study's outcomes.",{"count":82,"type":20},136,[23],"The study aims to assess whether the use of ultrasound during a pushing lesson can facilitate easier and safer childbirth. The research will be conducted at a single hospital and will involve pregnant women in their second trimester who enroll in an online childbirth course. Participants will be randomly assigned to one of two groups:\n\nOne group will receive standard pushing instructions from a midwife.\n\nThe other group will receive the same instructions along with a brief ultrasound session to visually support correct pushing techniques.\n\nThe primary outcome is a potential reduction in the duration of the second stage of labor (when the baby is being delivered). Secondary outcomes include improved coordination of pelvic floor muscles, fewer perineal tears, a higher rate of vaginal births, reduced postnatal urinary incontinence, and greater maternal satisfaction.\n\nApproximately 136 women will be enrolled in the study (accounting for potential dropouts). The expectation is that this integrated teaching approach will enhance the effectiveness, safety, and overall experience of pushing during labor for both mothers and their newborns.",[86,87,88,89,27,90],"Transperineal Ultrasound","Midwife-led Pushing Training Program","Duration of the Second Stage","Coactivation Rates of Pelvic Floor Muscles","Perineal Tear Rates","RECRUITING","2025-08-18",{"date":94,"type":32},"2025-08-22",{"date":96,"type":32},"2025-07-19",{"date":98,"type":20},"2026-05-27",{"name":100,"class":39},"Fondazione Policlinico Universitario Agostino Gemelli IRCCS"]