[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"breastfeeding-support\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:breastfeeding-support":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,49,77,103],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":29,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100606533","pregnancy-and-postpartum-breastfeeding-support-for-patients-with-gestational-diabetes-100606533",false,"NCT07176793","Pregnancy and Postpartum Breastfeeding Support for Patients With Gestational Diabetes","Preventing Type 2 Diabetes Following Gestational Diabetes: Implementation Mapping for a Multilevel Breastfeeding Support Strategy","Inclusion Criteria:\n\n* ≥18 years old and able to communicate in English\n* Fits into one of the following:\n\n  1. patients with GDM who are recently pregnant and\u002For postpartum;\n  2. health care providers (nurses, physicians, lactation consultants, etc.) who would implement the strategy\n  3. executive leadership\n\nExclusion Criteria:\n\n* Subjects not meeting the inclusion criteria will be considered ineligible for participation",true,"ALL","18 Years",{"count":20,"type":21},10,"ESTIMATED","OBSERVATIONAL","The investigators will use implementation methods to develop better breastfeeding support for patients with gestational diabetes as a way to prevent type 2 diabetes.",[25,26,27,28],"Gestational Diabetes Mellitus (GDM)","Diabetes Type 2","Breastfeeding Continuation","Breastfeeding Support",[30,31,32,33,34,35],"Gestational Diabetes","Preventing Diabetes Type 2 after GDM","Breastfeeding","Focus Groups","Implementation mapping","Breastfeeding support strategy","RECRUITING","2026-04-01",{"date":39,"type":40},"2026-04-07","ACTUAL",{"date":42,"type":40},"2026-03-23",{"date":44,"type":21},"2026-06-30",{"name":46,"class":47},"University of California, Davis","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":16,"sex":57,"minAge":18,"maxAge":4,"enrollmentInfo":58,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":60,"conditions":61,"keywords":64,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":48},"100631345","peer-support-breastfeeding-program-for-mothers-in-severe-socioeconomic-deprivation-feasibility-study-100631345","NCT07499466","Peer-Support Breastfeeding Program for Mothers in Severe Socioeconomic Deprivation: Feasibility Study","Feasibility Study of a Peer-Support Breastfeeding Resource and Support Program for Mothers Experiencing Severe Socioeconomic Deprivation","PARTAGE","Inclusion Criteria:\n\n* Mother with at least one infant hospitalized in the maternity or neonatal unit at the Hôpital Femme Mère Enfant (HFME)\n* Who Intents to breastfeed\n* Who is in a severe socioeconomic deprivation\n* Having sufficient proficiency in French or in one of the languages spoken by the available peer supporters to allow communication\n* Aged 18 years or older\n* Given verbal consent to participate in the study\n\nExclusion Criteria:\n\n* \\- Having a medical contraindication to breastfeeding\n* Having an infant with a known congenital condition with life-threatening prognosis\n* Having a severe psychiatric condition considered incompatible with participation in the peer-support intervention\n* Being under legal guardianship","FEMALE",{"count":59,"type":21},50,"Breastfeeding provides well-established and \"irreplaceable\" health benefits for both mothers and infants. However, breastfeeding rates in France remain among the lowest in Europe and are strongly associated with socioeconomic status. Mothers experiencing severe socioeconomic deprivation, including those facing housing instability or migration-related challenges, may encounter additional barriers to breastfeeding, such as social isolation, limited access to health information, and linguistic or cultural obstacles.\n\nPeer and community support have been shown to positively influence breastfeeding initiation and continuation. The Relais Allaitement Program (PRALL) is a peer-support program designed to promote breastfeeding and support early parenting through trained volunteer mothers. The PARTAGE project aims to adapt and pilot the PRALL program for mothers experiencing severe socioeconomic deprivation receiving care at the maternity unit of the Hôpital Femme Mère Enfant (HFME), in Bron, France.\n\nThis prospective, interventional, non-comparative feasibility study will evaluate the acceptability and feasibility of a peer-support breastfeeding program delivered by trained experienced mothers (peer supporters).\n\nThe intervention includes:\n\n* the adaptation of PRALL educational materials and training to the needs of vulnerable populations using participatory approaches and accessible communication principles,\n* the recruitment and training of two nursery nurses from the maternity unit to become network coordinators of the peer-support network,\n* the recruitment of experienced mothers who will be trained by the 2 network coordinators, to become breastfeeding peer supporters,\n* and the implementation of breastfeeding support by peer supporters for eligible mothers.\n\nEligible mothers experiencing severe socioeconomic deprivation will be offered support from a trained peer supporter during the postpartum period.\n\nThe primary outcome is the number of completed support interventions, defined as to have at least two in-person mother\u002Fpeer supporter contacts and to last at least one month, unless breastfeeding cessation or infant death occurs earlier. Qualitative interviews with participating mothers and peer supporters will also be conducted to explore barriers and facilitators to breastfeeding support in this population.\n\nThe results will inform the adaptation of the PRALL program for vulnerable populations and assess the feasibility of implementing a peer-support breastfeeding intervention in this context. Findings may guide the development of a larger multicenter study to evaluate the impact of peer-support programs on breastfeeding outcomes among socially disadvantaged populations in France and potentially across Europe.",[32,28,62,63],"Health Disparities","Health Inequalities",[65,66,67],"Peer support","Breastfeeding promotion","Socially deprived mothers","2026-03-24",{"date":70,"type":40},"2026-03-30",{"date":72,"type":40},"2025-12-01",{"date":74,"type":21},"2027-12-01",{"name":76,"class":47},"Hospices Civils de Lyon",{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":16,"sex":17,"minAge":83,"maxAge":4,"enrollmentInfo":84,"targetDuration":4,"studyType":86,"phases":87,"briefSummary":89,"conditions":90,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":102},"100586899","breastfeeding-intervention-to-prevent-obesity-among-children-100586899","NCT06921382","Breastfeeding Intervention to Prevent Obesity Among Children","Mothers and infants are both participants in the study. By the time study activities start, infants will be around 5 days old.\n\nInclusion Criteria Set 1 (determined at prenatal recruitment):\n\n1. Confirmation of Hispanic origin\n2. Receives or eligible for WIC\n3. Mother is 18 years or older\n4. Singleton pregnancy\n5. Mother intends to breastfeed.\n\nInclusion Criteria Set 2 (determined after infants are born):\n\n1. Infant gestational age 37 weeks or more\n2. Normal infant birth weight (i.e., \\> 5 lbs 8 oz.)\n3. Breastfeeding has been initiated\n4. No congenital or other health issues (such as cleft palate) identified that require specific accommodations for feeding.\n\nExclusion Criteria:\n\n1. Mothers below 18 years of age.\n2. Mothers do not plan to breastfeed.\n3. Mothers not eligible to participate in the WIC program due to high household income\n4. Non-singleton pregnancy.","5 Days",{"count":85,"type":21},170,"INTERVENTIONAL",[88],"NA","The goal of this clinical trial is to learn how to improve exclusive breastfeeding rates. The main questions it aims to answer are:\n\nDo Hispanic mothers benefit from peer counseling support from peer counselors who can speak Spanish? Are mothers more likely to continue exclusive breastfeeding if additional funds are given so that the WIC exclusive breastfeeding package has the same cash value as the WIC formula feeding package?\n\nResearchers will compare participants in the intervention group (who receive peer counseling and additional funds) to a control group (who do not receive peer counseling or additional funds) to see if the intervention package improves breastfeeding rates.\n\nAll participants (intervention and control) will complete weekly surveys about their feeding experiences ($8 per week). Members of the research team will also take infant weight\u002Flength measurements at home (twice during the first month and then at 2, 4, and 6 months). Participants will be recruited during pregnancy and the study will last for the first 6 months after their babies are born. Mothers and their infants are both participants in the study.\n\nParticipants in the intervention condition will also be matched with Spanish-speaking peer counselors who will visit mothers at home regularly (weekly at the beginning of the study, monthly at the end of the study). In Month 1, mothers can choose to receive a $150 gift card or an electric breast pump. In Months 2-5, if infants are signed up for the WIC exclusive breastfeeding package, infants will receive $100 and mothers will receive $50. If infants are signed up for the WIC partial breastfeeding package, infants will receive $50 and mothers will receive $30.",[91,27,92,28],"Breastfeeding Self-Efficacy","Breastfeeding Duration","2025-08-04",{"date":95,"type":40},"2025-08-08",{"date":97,"type":40},"2025-03-17",{"date":99,"type":21},"2027-06-30",{"name":101,"class":47},"University of North Carolina, Greensboro",2,{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":108,"acronym":4,"eligibilityCriteria":109,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":110,"enrollmentInfo":111,"targetDuration":4,"studyType":86,"phases":113,"briefSummary":114,"conditions":115,"keywords":117,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":131,"locationsCount":48},"100579888","post-procedural-manual-manipulation-for-infant-ankyloglossia-100579888","NCT06830148","Post-Procedural Manual Manipulation for Infant Ankyloglossia","Effectiveness of Post-Procedural Manual Manipulation for Infant Ankyloglossia in Enhancing Breastfeeding and Reducing Revision Rates: A Prospective Randomized Trial","Inclusion Criteria:\n\n* infants less than 90 days old with ankyloglossia who undergo outpatient frenotomy using cold-steel scissors and will be exclusively or partially breastfed.\n\nExclusion Criteria:\n\n* infants older than 90 days, those who will be exclusively bottle fed, infants who undergo concomitant lip tie release, those who undergo laser frenotomy, and infants who have previously undergone a frenotomy.\n* infants with a gestational age of less than 36 weeks, those in the NICU or post-partum unit, infants who didn't receive the vitamin K injection, and those with congenital anomalies or medical conditions affecting breastfeeding","90 Days",{"count":112,"type":21},110,[88],"The goal of this randomized control trial is to determine the impact of post-frenotomy manual manipulation on revision rates and breastfeeding outcomes. We hypothesize that post-frenotomy manipulation will reduce the rate of sublingual frenulum regrowth, and subsequently frenotomy revision rates, thereby improving breastfeeding performance.\n\nInfants with ankyloglossia undergoing frenotomy will be randomized into two groups: the intervention group (post-frenotomy manipulation) and the control group (no intervention). Parents in the intervention group will be instructed to perform tongue stretching and suck \"re-training\" exercises four times daily for 2-3 weeks, beginning 24 hours post-procedure. To monitor adherence and assess any complications, investigators will conduct a follow-up phone call one week after the procedure. Parents in the control group will not be instructed to perform any post-procedural manipulation. All participants will have a mandatory in-person follow-up 2-3 weeks postoperatively, during which breastfeeding outcomes and the need for frenotomy revision will be evaluated.",[116,28],"Ankyloglossia",[118,119,120,121,122,123],"tongue tie","breastfeeding","exercises","infant","pediatric otolaryngology","frenotomy","2025-02-11",{"date":126,"type":40},"2025-02-17",{"date":128,"type":40},"2024-10-15",{"date":130,"type":21},"2025-11",{"name":132,"class":47},"Georgetown University"]