[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"postpartum-recovery\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:postpartum-recovery":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,53],{"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":4,"briefSummary":23,"conditions":24,"keywords":28,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100640532","labor-epidural-analgesia-and-mother-infant-bonding-after-vaginal-delivery-100640532",false,"NCT07582289","Labor Epidural Analgesia and Mother-Infant Bonding After Vaginal Delivery","Association Between Postpartum Recovery Quality Measured by ObsQoR-10 and Mother-Infant Bonding After Vaginal Delivery: The Role of Labor Epidural Analgesia","Inclusion Criteria:\n\n* Female participants aged 18 to 40 years\n* Term singleton pregnancy (≥37 weeks)\n* Planned vaginal delivery\n* ASA physical status II\n* Ability to understand Turkish\n* Written informed consent\n\nExclusion Criteria:\n\n* Contraindications to epidural analgesia including coagulopathy, anticoagulant use, infection, or increased intracranial pressure\n* Cesarean delivery\n* High-risk pregnancy\n* Neonatal intensive care unit requirement\n* Major depressive disorder\n* Anxiety disorder\n* Current psychotropic medication use","FEMALE","18 Years","40 Years",{"count":20,"type":21},140,"ESTIMATED","OBSERVATIONAL","This prospective observational cohort study aims to evaluate the association between postpartum recovery quality and mother-infant bonding in women undergoing vaginal delivery. Postpartum recovery quality will be assessed using the Obstetric Quality of Recovery-10 (ObsQoR-10) questionnaire, and mother-infant bonding will be evaluated using the Postpartum Bonding Questionnaire (PBQ).\n\nParticipants will be grouped according to routine clinical labor analgesia preference: women receiving labor epidural analgesia and women not receiving epidural analgesia. Additional assessments will include postpartum pain intensity, anxiety, depressive symptoms, and birth satisfaction.\n\nBaseline psychological assessments will be performed before delivery. The primary postpartum evaluation will be conducted between 6 and 24 hours after delivery. Exploratory follow-up assessments will be performed by telephone during postpartum week 2.\n\nThe study aims to better understand the relationship between labor analgesia, postpartum recovery, and early mother-infant bonding outcomes after vaginal delivery.",[25,26,27],"Postpartum Recovery","Mother-infant Bonding","Labor Pain",[29,30,31,32,33,34,35,25,36,37,38,39],"Labor Epidural Analgesia","Postpartum Bonding Questionnaire","PBQ","EPDS","STAIS-5","ObsQoR-10","Vaginal Birth","Maternal Bonding","Obstetric Anesthesia","Postpartum Anxiety","Postpartum Depression","NOT_YET_RECRUITING","2026-05-30",{"date":43,"type":44},"2026-06-03","ACTUAL",{"date":46,"type":21},"2026-05-15",{"date":48,"type":21},"2029-06-17",{"name":50,"class":51},"Ataturk University","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":57,"acronym":58,"eligibilityCriteria":59,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":60,"targetDuration":4,"studyType":62,"phases":63,"briefSummary":65,"conditions":66,"keywords":4,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":52},"100459255","delivering-empowering-conversations-about-obstetric-regional-anesthesia-for-underserved-minorities-100459255","NCT05260242","Delivering Empowering Conversations About Obstetric Regional Anesthesia for Underserved Minorities","DECORUM","Inclusion Criteria:\n\n* Parturient patients being admitted to the labor and delivery unit at The Mount Sinai Hospital.\n* Patients of age 18 or greater with a singleton fetus of at least 37 weeks of gestation that present in spontaneous labor, for induction of labor, or augmentation of labor.\n* Patients in the first stage of labor and who have consented for placement of a labor epidural.\n\nExclusion Criteria:\n\n* Patients who are in severe labor pain following verbal informed consent prohibiting them from participating in the discussion,\n* Patients who present with a coagulopathy or on anticoagulation medications that exclude them from receiving labor epidural analgesia,\n* Patients who do not consent to labor epidural placement, or if they are on a mid-wife service.\n* Patients that are converted to a cesarean delivery following trial of labor",{"count":61,"type":21},100,"INTERVENTIONAL",[64],"NA","Racial and ethnic disparities in obstetric anesthesia care remains persistent despite studies documenting its existence and calling for action. The goal of this study is to share disparity data with underserved minority groups being admitted to the labor and delivery unit for obstetric care, to reduce mistrust and misconceptions regarding obstetric anesthesia care, and to bridge the cultural gap between patient beliefs and safe anesthetic care and to empower patients through transparency and provide them with the information necessary to make informed decisions about their care, to improve health literacy, and to ultimately improve patient outcomes and satisfaction.",[25],"RECRUITING","2025-05-30",{"date":70,"type":44},"2025-06-04",{"date":72,"type":44},"2023-05-01",{"date":74,"type":21},"2026-05",{"name":76,"class":51},"Icahn School of Medicine at Mount Sinai"]