[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100640532":3},{"organization":4,"armGroups":7,"interventions":17,"overallOfficials":22,"centralContacts":27,"locations":36,"responsibleParty":50,"collaborators":10,"id":54,"slug":55,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":10,"eligibilityCriteria":60,"healthyVolunteers":56,"sex":61,"minAge":62,"maxAge":63,"enrollmentInfo":64,"targetDuration":10,"studyType":67,"phases":10,"briefSummary":68,"conditions":69,"keywords":73,"overallStatus":84,"whyStopped":10,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":94},{"fullName":5,"class":6},"Ataturk University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Labor Epidural Analgesia",null,"Women undergoing vaginal delivery with labor epidural analgesia as part of routine clinical care. Participants will undergo postpartum recovery, mother-infant bonding, anxiety, depression, pain, and birth satisfaction assessments during the postpartum period.",[13],"Procedure: Labor Epidural Analgesia",{"label":15,"type":10,"description":16,"interventionNames":10},"No Labor Epidural Analgesia","Women undergoing vaginal delivery without labor epidural analgesia as part of routine clinical care. Participants will be evaluated for postpartum recovery quality, mother-infant bonding, anxiety, depressive symptoms, pain intensity, and birth satisfaction during the postpartum period.",[18],{"type":19,"name":9,"description":20,"armGroupLabels":21,"otherNames":10},"PROCEDURE","Epidural analgesia administered during labor as part of routine clinical care for pain management during vaginal delivery.",[9],[23],{"name":24,"affiliation":25,"role":26},"Ayşe Ceren Hilal Güven, assistant doctor","Ataturk University Department of Anesthesiology and Reanimation","STUDY_CHAIR",[28,33],{"name":29,"role":30,"phone":31,"phoneExt":10,"email":32},"Ayşenur Dostbil, Associate Professor","CONTACT","+90 533 367 66 96","adostbil@hotmail.com",{"name":24,"role":30,"phone":34,"phoneExt":10,"email":35},"+90 554 112 25 81","achg1995@gmail.com",[37],{"facility":5,"status":10,"city":38,"state":10,"zip":39,"country":40,"countryCode":10,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"Erzurum","25000","Turkey (Türkiye)",{"type":42,"coordinates":43},"Point",[44,45],41.27694,39.90861,{"lat":45,"lon":44},[48],{"name":24,"role":30,"phone":49,"phoneExt":10,"email":35},"554-112-25-81",{"type":51,"investigatorFullName":52,"investigatorTitle":53,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"PRINCIPAL_INVESTIGATOR","Aysenur Dostbil","Associate Professor as the Principal Investigator","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":65,"type":66},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.",[70,71,72],"Postpartum Recovery","Mother-infant Bonding","Labor Pain",[9,74,75,76,77,78,79,70,80,81,82,83],"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":87,"type":88},"2026-06-03","ACTUAL",{"date":90,"type":66},"2026-05-15",{"date":92,"type":66},"2029-06-17",{"name":5,"class":6},1]