[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"breastfeeding-duration\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:breastfeeding-duration":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,66,104,131],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":44,"overallStatus":53,"whyStopped":4,"lastUpdateSubmitDate":54,"lastUpdatePostDateStruct":55,"startDateStruct":58,"completionDateStruct":60,"leadSponsor":62,"locationsCount":65},"100636706","improved-child-nutrition-and-development-through-social-transfers-100636706",false,"NCT07569172","Improved Child Nutrition and Development Through Social Transfers","Taabo Enhanced Nutrition and Development Through Economic Rewards","TENDER","Inclusion Criteria:\n\n1. Are enrolled in the Taabo multigenerational birth cohort (MGC)\n2. Completed the postpartum interview of the Taabo MGC\n3. Have a child who is within two weeks of their 12-month birthday,\n4. are breastfeeding at time of recruitment,\n5. live in the Taabo HDSS, Côte d'Ivoire\n6. have no illnesses that contraindicates breastfeeding,\n7. had a healthy singleton infant with a birth weight of at least 2500 grams, and\n8. agree to participate and sign an informed consent; if underage (12-17 years), a legal representative will also have to agree to sign the informed consent\n\nExclusion Criteria:\n\n1. Plans to move permanently outside study area\n2. Has a medical, intellectual or psychological disability\n3. Contraindication for breastfeeding\n4. Children born with \\\u003C 2500 grams","FEMALE","12 Years",{"count":20,"type":21},1040,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to learn if a conditional social transfer works to improve rates of complementary breastfeeding. It will also learn about the impacts of social transfers on maternal and child health and development. The main questions it aims to answer are:\n\n* Does the social transfer increase complementary breastfeeding rates at 24-months postpartum?\n* Does the social transfer increase complementary breastfeeding duration?\n* Does the social transfer impact child health and development?\n* Does the social transfer impact maternal physical and mental health?\n\nResearchers will compare a conditional social transfer to a control group that only receives education about breastfeeding recommendations to see if a conditional social transfers works to increase complementary breastfeeding.\n\nParticipants will:\n\nReceive a pamphlet explaining the current recommendations of breastfeeding Receive instructions that if they meet the recommendation to breastfeed until 24-months postpartum they receive a social transfer or receive no additional information Complete home visits at 12- and 24-months postpartum Complete detailed questionnaire",[27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43],"Breastfeeding","Breastfeeding Education","Breastfeeding Duration","Breastfeeding Continuation","Child Growth","Stress","Infectious Diseases","Anemia","Child Development","Weight Loss","Blood Pressure","Mental Health","Diarrhea","Coughing","Eczema","Allergies","Antibiotic Use",[45,46,47,48,49,50,51,52],"breastfeeding","cash transfer","child health","maternal health","mental health","child growth","child development","education","NOT_YET_RECRUITING","2026-04-28",{"date":56,"type":57},"2026-05-06","ACTUAL",{"date":59,"type":21},"2026-06-01",{"date":61,"type":21},"2028-02-28",{"name":63,"class":64},"Swiss Tropical & Public Health Institute","OTHER",1,{"id":67,"slug":68,"hasResults":11,"nctId":69,"briefTitle":70,"officialTitle":71,"acronym":72,"eligibilityCriteria":73,"healthyVolunteers":11,"sex":17,"minAge":74,"maxAge":4,"enrollmentInfo":75,"targetDuration":4,"studyType":22,"phases":77,"briefSummary":78,"conditions":79,"keywords":89,"overallStatus":53,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":65},"100616738","effectiveness-of-a-counseling-program-on-exclusive-breastfeeding-rates-in-a-primary-care-center-100616738","NCT07309510","Effectiveness of a Counseling Program on Exclusive Breastfeeding Rates in a Primary Care Center","Effectiveness of a Counseling Program on Exclusive Breastfeeding Rates in a Primary Care Center in A Coruña.Randomized Controlled Clinical Trial","ALM-AP","Inclusion Criteria:\n\n* Mothers who express a desire to breastfeed during a follow-up consultation with the Obstetric and Gynecological Nursing specialist at 36 weeks of gestation.\n* Mothers who plan to give birth at HMI of CHUAC, referred from the C.S. Ventorrillo.\n* Women who are fluent in Spanish or Galician.\n\nExclusion Criteria:\n\n* Maternal age under 18 years - Maternal use of drugs or medication that prevent breastfeeding .\n* Maternal infection with HIV or Human T-cell Leukemia Virus.\n* Mothers of newborns with cow's milk protein allergy, galactosemia, or congenital primary lactase deficiency.","18 Years",{"count":76,"type":21},160,[24],"Introduction: Evidence supports that exclusive breastfeeding (EBF) is the most beneficial method of infant feeding up to 6 months of age. The practice confers numerous advantages for the infant and the mother. Many breasfeeding are abandoned early due difficulties experienced after dischargue and after returning to work. Development specific early breastfeeding support programs in the community is necessary to avoid unwanted abandonment.\n\nObjective: To analyse the differences in BF rates at six month of birth in healthy full-term newborns between the study groups.\n\nMethodology: Pilot study of a randomised clinical trial carried out in a Paediatric Nursing clinic at the Ventorrillo Health Centre in A Coruña. The study population will be mothers of healthy full-term newborns who wish to give BF at the time of delivery and whose reference health centre is the one of the study. The mother- newborn dyads in the control group (CG) will receive the usual care described in the child health Program of the Galician Health Service, and the dyads included in the intervention group (IG) will also receive specific advice on breastfeeding during the first 6 months of life. A study sample of 80 participants is estimated for each group. The study will be approved by the Research Ethics Committee of A Coruña-Ferrol. The variables under study will be collected in a data collection notebook for later statistical analysis. A significant value of p \\\u003C 0.05 being considered.",[80,81,82,29,83,84,85,86,87,88],"Growth & Development","Breastfeeding Satisfaction","Breastfeeding Consultancy Training","Breastfeeding After Discharge From Hospital Following Childbirth, Yes\u002Fno","Breastfeeding, Exclusive","Breastfeeding Attitude","Breastfeeding Support System","Breastfeeding Rate","Breastfeeding Outcomes",[27,90,91,92,93,94],"Infant","Human Milk","Health Education","Primary Health Care","Postpartum Period","2026-01-07",{"date":97,"type":57},"2026-01-08",{"date":99,"type":21},"2026-01",{"date":101,"type":21},"2027-01",{"name":103,"class":64},"Fundacion Profesor Novoa Santos",{"id":105,"slug":106,"hasResults":11,"nctId":107,"briefTitle":108,"officialTitle":108,"acronym":4,"eligibilityCriteria":109,"healthyVolunteers":110,"sex":111,"minAge":112,"maxAge":4,"enrollmentInfo":113,"targetDuration":4,"studyType":22,"phases":115,"briefSummary":116,"conditions":117,"keywords":4,"overallStatus":120,"whyStopped":4,"lastUpdateSubmitDate":121,"lastUpdatePostDateStruct":122,"startDateStruct":124,"completionDateStruct":126,"leadSponsor":128,"locationsCount":130},"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.",true,"ALL","5 Days",{"count":114,"type":21},170,[24],"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.",[118,30,29,119],"Breastfeeding Self-Efficacy","Breastfeeding Support","RECRUITING","2025-08-04",{"date":123,"type":57},"2025-08-08",{"date":125,"type":57},"2025-03-17",{"date":127,"type":21},"2027-06-30",{"name":129,"class":64},"University of North Carolina, Greensboro",2,{"id":132,"slug":133,"hasResults":11,"nctId":134,"briefTitle":135,"officialTitle":135,"acronym":136,"eligibilityCriteria":137,"healthyVolunteers":110,"sex":17,"minAge":74,"maxAge":4,"enrollmentInfo":138,"targetDuration":4,"studyType":140,"phases":4,"briefSummary":141,"conditions":142,"keywords":148,"overallStatus":120,"whyStopped":4,"lastUpdateSubmitDate":150,"lastUpdatePostDateStruct":151,"startDateStruct":153,"completionDateStruct":155,"leadSponsor":157,"locationsCount":65},"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":139,"type":21},1628,"OBSERVATIONAL","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.",[27,143,29,144,145,146,147],"Breastfeeding Initiation","Birth","Birth Practices","Gestational Diabetes Mellitus (GDM)","Preeclampsia",[149,45],"Birth, birth practices, gestational diabetes, preeclampsia","2025-05-22",{"date":152,"type":57},"2025-05-28",{"date":154,"type":57},"2025-01-06",{"date":156,"type":21},"2028-01",{"name":158,"class":64},"Herlev Hospital"]