[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"maternal-fetal-attachment\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:maternal-fetal-attachment":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,52],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":32,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":51},"100629720","hybrid-breastfeeding-education-in-late-pregnancy-effects-on-antenatal-attachment-and-breastfeeding-100629720",false,"NCT07478341","Hybrid Breastfeeding Education in Late Pregnancy: Effects on Antenatal Attachment and Breastfeeding","The Effect of Individualized Hybrid Breastfeeding Education in Late Pregnancy on Antenatal Attachment and Breastfeeding Behaviors in Primiparous Women","Inclusion Criteria:\n\nAged 18-35 years,\n\nAt 36 weeks of gestation or later,\n\nExperiencing their first pregnancy (primiparous),\n\nHaving a singleton pregnancy,\n\nAble to read and write in Turkish and capable of communication,\n\nHaving access to a smartphone or the internet,\n\nFree from any physical or mental health problems that would prevent participation in the education,\n\nWilling to voluntarily participate in the study and provide written informed consent.\n\nExclusion Criteria:\n\nPresence of chronic physical illness or pregnancy complications (e.g., preeclampsia, gestational diabetes),\n\nMultiple pregnancy,\n\nGestation earlier than 36 weeks,\n\nInability to actively participate in the education due to communication barriers or cognitive impairment,\n\nLack of access to a smartphone or the internet,\n\nFailure to attend any stage of the educational program or voluntary withdrawal from the study,\n\nRefusal to participate in the study or failure to sign the informed consent form.",true,"FEMALE","18 Years","35 Years",{"count":21,"type":22},64,"ESTIMATED","INTERVENTIONAL",[25],"NA","This randomized controlled study aims to examine the effect of individualized hybrid breastfeeding education provided during late pregnancy on antenatal attachment and breastfeeding behaviors among first-time mothers. Participants will be randomly assigned to either the intervention or control group. Women in the intervention group will receive individualized hybrid breastfeeding education beginning at the 36th week of pregnancy. The program includes a face-to-face individual breastfeeding education session at 36 weeks of pregnancy and a reinforcement and practice session at 38 weeks. Participants will also have access to personalized digital educational materials, short educational videos, and online consultation support. In the postpartum period, participants will receive an online support session during the first week after birth and a follow-up session through online communication or telephone at the sixth postpartum week. The control group will receive routine hospital education during pregnancy. After completion of the study, the same educational materials will be provided to the control group in accordance with ethical principles. Data will be collected using the Demographic Information Form, Breastfeeding Behavior Evaluation Form, Antenatal Attachment Inventory, and Breastfeeding Self-Efficacy Scale. Written informed consent will be obtained from all participants prior to enrollment.",[28,29,30,31],"Breast Feeding","Exclusive Breast Feeding","Maternal-Fetal Attachment","Primiparity",[33,34,35,36,37,38],"Breastfeeding Education","Hybrid Education","Primiparous Women","Antenatal Attachment","Breastfeeding Self-Efficacy","Mother-Infant Bonding","RECRUITING","2026-03-13",{"date":42,"type":43},"2026-03-17","ACTUAL",{"date":45,"type":43},"2025-12-30",{"date":47,"type":22},"2026-08-01",{"name":49,"class":50},"Emel GÜÇLÜ CİHAN","OTHER",1,{"id":53,"slug":54,"hasResults":11,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":4,"eligibilityCriteria":58,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":59,"enrollmentInfo":60,"targetDuration":4,"studyType":23,"phases":62,"briefSummary":63,"conditions":64,"keywords":67,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":4},"100625034","prenatal-haptonomy-based-support-100625034","NCT07417384","Prenatal Haptonomy-Based Support","Effects of Haptonomy-Based Support Approaches in the Prenatal Period on Prenatal Attachment and Perceived Partner Support - A Randomized Controlled Study","Inclusion Criteria:\n\n* Pregnant women aged 18-45 years\n* Attending antenatal follow-up at Tokat Gaziosmanpaşa University Hospital\n* Gestational age between 20 and 32 weeks\n* Ability to communicate in Turkish\n* Willingness to participate and provide written informed consent\n\nExclusion Criteria:\n\n* High-risk pregnancy (e.g., preeclampsia, placenta previa, gestational diabetes requiring insulin)\n* Diagnosed psychiatric disorder\n* Multiple pregnancy\n* Known fetal anomaly\n* Participation in another interventional study","45 Years",{"count":61,"type":22},36,[25],"This study is a three-arm randomized controlled trial to be conducted among pregnant women attending the antenatal outpatient clinic of Tokat Gaziosmanpaşa University Hospital who meet the inclusion criteria. Data will be collected between April 1, 2026, and April 30, 2027.\n\nEligible participants will be informed about the study objectives, procedures, potential benefits and risks, and voluntary participation principles. Written informed consent will be obtained prior to enrollment. Participant confidentiality will be ensured in accordance with data protection regulations, and unique identification codes will be assigned.\n\nAt baseline (T0), participants will complete the Personal Information Form, Prenatal Attachment Inventory (PAI), and Spousal Support Scale (SSS). Following baseline assessment, participants will be randomly allocated into one of three groups:\n\nPartner-supported haptonomy group Mother-supported haptonomy group Midwife-supported haptonomy group The haptonomy-based intervention will be delivered once weekly for three consecutive weeks in a hospital-based setting. Each session will last approximately 30 minutes and will follow a standardized protocol including structured affective touch, body awareness facilitation, emotional observation, and structured session closure. All sessions will be conducted by a research assistant who completed the Prenatal Haptonomy Instructor Training (January 29-31, 2026). The principal investigator will supervise and monitor the scientific integrity of the study.\n\nOutcome assessments will be conducted at three time points:\n\nT0 (Baseline): Prior to intervention T1 (Post-session 1): 24-48 hours after the first haptonomy session T2 (Post-intervention): 24-48 hours after the third haptonomy session The Prenatal Attachment Inventory and Spousal Support Scale will be re-administered at T1 and T2. Data completeness will be checked after each assessment.",[30,65,66],"Perceived Partner Support","Haptonomy",[66,68,69,30,70,71,72,73,74],"Prenatal Haptonomy","Prenatal Attachment","Partner Support; Pregnancy","Randomized Controlled Trial","Psychosocial Intervention","Partner Support","Pregnancy","NOT_YET_RECRUITING","2026-02-27",{"date":78,"type":43},"2026-03-02",{"date":80,"type":22},"2026-04-01",{"date":82,"type":22},"2027-04-30",{"name":84,"class":50},"Hilal Özbek"]