[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"breastfeeding-initiation\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:breastfeeding-initiation":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,55,83],{"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":35,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":49,"leadSponsor":51,"locationsCount":54},"100648425","breastfeeding-education-integrated-with-web-portal-and-mobile-application-supported-counseling-100648425",false,"NCT07721311","Breastfeeding Education Integrated With Web Portal and Mobile Application-Supported Counseling","The Effect of Breastfeeding Education Integrated With Web Portal and Mobile Application-Supported Counseling on Perceived Insufficient Milk Supply, Breastfeeding Intention, and Breastfeeding Adaptation: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Pregnant women at 37-39 weeks of gestation.\n* Being 18 years of age or older.\n* Planning to give birth at the study hospital.\n* Planning to breastfeed their newborn.\n* Having a singleton pregnancy.\n* Having a healthy pregnancy without conditions requiring high-risk pregnancy management.\n* Being able to communicate verbally and understand the study procedures.\n* Having access to a smartphone and\u002For internet connection to use the web portal and mobile application (for participants assigned to the intervention group).\n* Voluntarily agreeing to participate in the study and providing written informed consent.\n\nExclusion Criteria:\n\n* Having a medical condition that contraindicates breastfeeding.\n* Having a pregnancy complication requiring intensive medical follow-up or early delivery.\n* Multiple pregnancy (e.g., twins or higher-order pregnancies).\n* Planned cesarean delivery due to medical indications that may interfere with the breastfeeding initiation process (if applicable according to your protocol).\n* Having a newborn requiring neonatal intensive care admission after birth.\n* Previous participation in a structured breastfeeding education or digital breastfeeding counseling program during the current pregnancy.\n* Inability to complete study questionnaires or participate in follow-up assessments.\n* Not having access to the required digital tools for the intervention group.\n* Withdrawal of informed consent at any stage of the study.",true,"FEMALE","18 Years","49 Years",{"count":21,"type":22},62,"ESTIMATED","INTERVENTIONAL",[25],"NA","Breastfeeding provides significant benefits for maternal and infant health; however, perceived insufficient milk supply is one of the most common factors associated with early breastfeeding discontinuation. Although the World Health Organization recommends exclusive breastfeeding for the first six months of life, breastfeeding continuation rates remain suboptimal in many countries, including Türkiye.\n\nThis randomized controlled trial aims to evaluate the effect of breastfeeding education combined with a web portal and mobile application-supported breastfeeding counseling on perceived insufficient milk supply, breastfeeding intention, and breastfeeding adaptation among pregnant women.\n\nWomen at 37-39 weeks of gestation will be randomly assigned to an intervention group or a control group. Participants in the intervention group will receive individualized breastfeeding education during pregnancy, educational materials, postpartum breastfeeding support, and web portal- and mobile application-supported breastfeeding counseling. Participants in the control group will receive routine hospital care.\n\nData will be collected during pregnancy (baseline), immediately after birth, and at 1-, 3-, and 6-month postpartum follow-ups using validated scales assessing perceived insufficient milk supply, breastfeeding intention, and breastfeeding adaptation. Digital platform usage data, including the counseling topics accessed and the frequency of use, will also be evaluated in the intervention group.\n\nThis study is supported as a research project and aims to develop an accessible digital breastfeeding support model that may improve breastfeeding confidence, reduce perceived insufficient milk supply, and promote breastfeeding adaptation and continuation.",[28,29,30,31,32,33,34],"Breastfeeding","Breastfeeding Attitudes","Breastfeeding Education","Breastfeeding Initiation","Breastfeeding Support","Breastfeeding Consultancy Training","Breastfeeding Outcomes",[36,37,38,39,40,41],"Breastfeeding education","Breastfeeding Counseling","Perception of Insufficient Milk Supply","Web Portal Support","Breastfeeding Adaptation","Mobile Application","RECRUITING","2026-08-19",{"date":45,"type":46},"2026-08-20","ACTUAL",{"date":48,"type":46},"2026-07-20",{"date":50,"type":22},"2027-02-20",{"name":52,"class":53},"Aydin Adnan Menderes University","OTHER",1,{"id":56,"slug":57,"hasResults":11,"nctId":58,"briefTitle":59,"officialTitle":60,"acronym":61,"eligibilityCriteria":62,"healthyVolunteers":16,"sex":17,"minAge":63,"maxAge":19,"enrollmentInfo":64,"targetDuration":4,"studyType":66,"phases":4,"briefSummary":67,"conditions":68,"keywords":70,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":4},"100618775","breastfeeding-influencing-determinants-knowledge-and-self-efficacy-100618775","NCT07336004","Breastfeeding: Influencing Determinants, Knowledge and Self-efficacy","Breastfeeding: Influencing Determinants, Knowledge and Self-efficacy Among Lactating Mothers in Sohag Governorate","feeding","Inclusion criteria:\n\n• The study will include lactating mothers with children from day zero to 24 months.\n\nExclusion criteria:\n\n* Mothers with absolute contraindications to breastfeeding as the infant having classic galactosemia\n* The mother having human immunodeficiency virus (HIV) will be excluded from the study.","15 Years",{"count":65,"type":22},380,"OBSERVATIONAL","Our study will assess the prevalence of exclusive breastfeeding and the determinants and assess knowledge and self efficacy of lactating mothers towards breastfeeding",[69,31],"Breastfeeding, Exclusive",[71,72],"breastfeeding","Beastfeeding exclusivness","NOT_YET_RECRUITING","2026-01-10",{"date":76,"type":46},"2026-01-13",{"date":78,"type":22},"2026-01-01",{"date":80,"type":22},"2027-03-01",{"name":82,"class":53},"Sohag University",{"id":84,"slug":85,"hasResults":11,"nctId":86,"briefTitle":87,"officialTitle":87,"acronym":88,"eligibilityCriteria":89,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":90,"targetDuration":4,"studyType":66,"phases":4,"briefSummary":92,"conditions":93,"keywords":99,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":54},"100580954","birth--breastfeeding-support-study-100580954","NCT06844019","Birth & Breastfeeding Support Study","BABSS","Inclusion Criteria: 18 years, intention to breastfeed, single gestation, reads and understands Danish -\n\nExclusion Criteria: Twin gestation, less than 18 years, no intention to breastfeed, does not read and understand Danish\n\n\\-",{"count":91,"type":22},1628,"The goal of this observational study is to learn about the effects of birth practices such as cesarean section and vacuum assisted birth and diseases such as gestational diabetes and preeclampsia on exclusive breastfeeding. The main question it aims to answer is:\n\n• Does cesarean section, vacuum assisted birth, gestational diabetes and preeclampsia affect exclusive breastfeeding three months after birth? Participants answer eight online survey questions. One survey is distributed before birth and the remaining seven surveys are distributed after birth at three, seven and four-teen days, as well as one, three, six and twelve months after birth.",[28,31,94,95,96,97,98],"Breastfeeding Duration","Birth","Birth Practices","Gestational Diabetes Mellitus (GDM)","Preeclampsia",[100,71],"Birth, birth practices, gestational diabetes, preeclampsia","2025-05-22",{"date":103,"type":46},"2025-05-28",{"date":105,"type":46},"2025-01-06",{"date":107,"type":22},"2028-01",{"name":109,"class":53},"Herlev Hospital"]