[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"maternal-health-education\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:maternal-health-education":52},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":14,"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":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":5},"100637669",false,"NCT07593716","Effect of a Self-Efficacy-Based Educational Intervention on Breastfeending in Primigravid Women: A Randomized Controlled Trial","Effect of a Self-Efficacy-Based Educational Intervention on Exclusive Breastfeeding in Primigravid Women Attending a Primary Care Center: A Randomized Controlled Trial","PROMILACT","Inclusion Criteria:\n\n* Pregnant women aged 18 years or older\n* Primigravidae in the third trimester of pregnancy\n* Receiving prenatal care at UMF No. 9, IMSS\n* Ability to attend the educational sessions\n* Willingness to participate and sign informed consent\n\nExclusion Criteria:\n\n* High-risk pregnancy\n* Medical conditions contraindicating breastfeeding\n* Cognitive impairment or communication difficulties preventing participation\n* Previous participation in breastfeeding educational programs\n* Failure to complete follow-up evaluations",true,"FEMALE","18 Years","45 Years",{"count":21,"type":22},160,"ESTIMATED","INTERVENTIONAL",[25],"NA","This randomized controlled trial aims to evaluate the effect of a self-efficacy-based educational intervention on exclusive breastfeeding among primigravid women attending a primary care center in Mexico. Participants in the intervention group will receive four weekly educational sessions focused on breastfeeding knowledge, self-efficacy, problem-solving skills, and emotional support during the third trimester of pregnancy. The control group will receive standard prenatal care. Breastfeeding self-efficacy and exclusive breastfeeding rates will be evaluated during postpartum follow-up at 1 and 3 months after delivery.",[28,29,30,31],"Exclusive Breastfeeding","Breastfeeding Self-Efficacy","Pregnancy","Maternal Health Education",[33,34,35,36,37,38,39],"Breastfeeding","Primigravid Women","Educational Intervention","Randomized Controlled Trial","BSES-SF","Primary Care","Mexico","NOT_YET_RECRUITING","2026-05-12",{"date":43,"type":44},"2026-05-18","ACTUAL",{"date":46,"type":22},"2026-05",{"date":48,"type":22},"2027-08",{"name":50,"class":51},"Instituto Mexicano del Seguro Social","OTHER_GOV",""]