[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"maternal-nutrition\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:maternal-nutrition":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,50,76,100],{"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":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":4},"100644157","mms-ifa-and-mmsifa-supplementation-in-pregnant-women-100644157",false,"NCT07665957","MMS, IFA, and MMS+IFA Supplementation in Pregnant Women","Comparative Effectiveness of Multiple Micronutrient Supplementation (MMS), Iron-Folic Acid (IFA), and Combined MMS+IFA on Maternal Hemoglobin Levels and Neonatal Outcomes Among Pregnant Women: An Open-Label Randomized Controlled Trial","Inclusion Criteria:\n\n* Pregnant women aged 18 years or older\n* Gestational age ≤20 weeks at enrollment\n* Singleton pregnancy\n* Hemoglobin concentration ≥10 g\u002FdL at baseline\n* Willing and able to provide informed consent\n* Willing to comply with study procedures and follow-up visits\n\nExclusion Criteria:\n\n* Severe anemia requiring injectable treatment (hemoglobin \\\u003C7 g\u002FdL)\n* Pre-existing diabetes mellitus\n* Pre-existing hypertension\n* Renal disease\n* Current therapeutic iron or micronutrient supplementation beyond routine antenatal supplementation\n* Known fetal congenital anomalies\n* Any medical condition that, in the opinion of the investigator, would interfere with study participation or outcome assessment",true,"FEMALE","18 Years",{"count":20,"type":21},402,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study aims to compare the effectiveness of Multiple Micronutrient Supplementation (MMS), Iron-Folic Acid (IFA) supplementation, and combined MMS+IFA supplementation among pregnant women. Maternal anemia and micronutrient deficiencies are common during pregnancy and can adversely affect both maternal and neonatal health outcomes.\n\nA total of 402 pregnant women with gestational age of 20 weeks or less will be randomly assigned to receive MMS, IFA, or combined MMS+IFA supplementation. Participants will be followed throughout pregnancy until delivery. Maternal hemoglobin levels, maternal compliance with supplementation, and neonatal outcomes including birth weight, preterm birth, APGAR scores, and congenital anomalies will be assessed.\n\nThe findings of this study will provide evidence to guide antenatal nutrition policies and practices in Pakistan.",[27,28,29,30],"Maternal Anemia","Micronutrient Deficiency","Pregnancy Outcomes","Maternal Nutrition",[32,33,34,35,36,27,37,30],"Multiple Micronutrient Supplementation","MMS","Iron Folic Acid","IFA","Pregnancy","Maternal Hemoglobin","NOT_YET_RECRUITING","2026-06-27",{"date":41,"type":42},"2026-07-01","ACTUAL",{"date":44,"type":21},"2026-06-25",{"date":46,"type":21},"2027-01-25",{"name":48,"class":49},"Sindh Institute of Child Health and Neonatology","OTHER",{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":56,"eligibilityCriteria":57,"healthyVolunteers":16,"sex":17,"minAge":58,"maxAge":59,"enrollmentInfo":60,"targetDuration":4,"studyType":22,"phases":62,"briefSummary":63,"conditions":64,"keywords":4,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":75},"100633081","social-networks-for-improving-maternal--child-health-100633081","NCT07522047","Social Networks for Improving Maternal & Child Health","Improving the Health and Nutritional Status of Mothers and Children Using Indigenous Community Structure in Northwest Ethiopia","SoNIMCH","Inclusion Criteria:\n\nPregnant women residing in the selected study clusters (kebeles)\n\nPregnant women who are in their first trimester (gestational age less than 16 weeks) at the time of recruitment.\n\nPregnant women who intend to reside in the study area for the duration of the pregnancy and at least six months postpartum.\n\nExclusion Criteria:\n\nPregnant women with known pre-existing chronic medical conditions (e.g., chronic hypertension, diabetes mellitus, or cardiac disease) that require specialized medical management.\n\nPregnant women who are unable to communicate or undergo the interview process due to severe illness or cognitive impairment.\n\nPregnant women who are already participating in another clinical trial or health intervention study.","15 Years","49 Years",{"count":61,"type":21},700,[24],"Brief Summary: Improving Maternal and Child Health via Indigenous Structures\n\nThe goal of this cluster randomized controlled community trial is to assess the effect of community-based interventions using indigenous community structures on the improvement of health and nutritional status in pregnant women (recruited before 16 weeks of gestation) and their children in Northwest Ethiopia. The main questions it aims to answer are:\n\n* Does a community-based intervention using indigenous structures significantly improve the uptake of maternal health services (ANC, delivery, and PNC)?\n* Does the intervention effectively reduce the prevalence of maternal depression during the pregnancy and postpartum periods?\n* To what extent does the intervention improve the nutritional status (reducing thinness and stunting) of mothers and their children? Researchers will compare a group of women receiving counseling from trained indigenous social support groups to a control group receiving only the routine health and nutrition education provided by the standard healthcare system to see if the indigenous approach leads to better health and nutritional outcomes.\n\nParticipants will:\n\n* Receive four counseling sessions during pregnancy (starting before 16 weeks of gestation) and four additional sessions during the lactation period, conducted in their homes by trained social support groups.\n* Receive educational leaflets containing core health and nutrition messages and appropriate pictures.\n* Participate in two rounds of surveys (baseline, and endline) involving interviewer-administered questionnaires.\n* Undergo physical measurements, specifically mid-upper arm circumference (MUAC), to assess nutritional status.",[65,30],"Maternal and Child Health","2026-04-03",{"date":68,"type":42},"2026-04-13",{"date":70,"type":21},"2026-04-01",{"date":72,"type":21},"2028-06-30",{"name":74,"class":49},"Bahir Dar University",1,{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":83,"targetDuration":4,"studyType":85,"phases":4,"briefSummary":86,"conditions":87,"keywords":4,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":75},"100629625","longitudinal-prospective-study-of-maternal-and-child-nutrition-in-arkansas-100629625","NCT07477106","Longitudinal Prospective Study of Maternal and Child Nutrition in Arkansas","Longitudinal Prospective Study of Maternal and Child Nutrition in Arkansas - The Thrive Study","Inclusion Criteria:\n\n* At least 30 weeks pregnant\n* Ability to engage in study procedures throughout the first 12 months postpartum\n\nExclusion Criteria:\n\n* None",{"count":84,"type":21},125,"OBSERVATIONAL","The investigators want to learn how women's diets may impact breastfeeding outcomes. This study will help the investigators learn more about how diet and social factors like food access may impact mothers' health, breastfeeding, and their baby's health. Participants will attend a visit before birth, then 11 visits as their baby grows up. All visits will be remote using RedCap, phone or video call, text messaging or any other communication modalities of preference to the participant. The investigators will ask for personal information about participants' family, home, and finances, health literacy, medical history, current medications, pregnancy complications, mental health (depression, quality of life), confidence in breastfeeding, eating habits, and plan to feed their baby. After childbirth, the investigators will ask about participants' delivery and child's health, and request access to their child's medical records. Across all visits, the investigators will ask participants to measure their weight, height, blood pressure, activity and sleep, and child's length; the investigators will also ask them to ship urine, stool, and breast milk samples. The investigators will obtain a 24-hour feeding log for the child, as well as a log of what the mother ate and drank over 24 hours.",[30,88,89,90],"Infant Nutrition","Pediatric Nutrition","Maternal Health","2026-03-13",{"date":93,"type":42},"2026-03-17",{"date":95,"type":21},"2026-05",{"date":97,"type":21},"2029-06",{"name":99,"class":49},"Arkansas Children's Hospital Research Institute",{"id":101,"slug":102,"hasResults":11,"nctId":103,"briefTitle":104,"officialTitle":105,"acronym":4,"eligibilityCriteria":106,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":107,"enrollmentInfo":108,"targetDuration":4,"studyType":22,"phases":110,"briefSummary":111,"conditions":112,"keywords":114,"overallStatus":118,"whyStopped":4,"lastUpdateSubmitDate":119,"lastUpdatePostDateStruct":120,"startDateStruct":122,"completionDateStruct":124,"leadSponsor":126,"locationsCount":128},"100561765","healthy-baby-healthy-mother-toolkit-100561765","NCT06594419","Healthy Baby Healthy Mother Toolkit","Efficacy of the Healthy Mother Healthy Baby Toolkit for Maternal and Child Nutrition in Ethiopia","Inclusion Criteria:\n\n* \\\u003C20 weeks gestation as determined by maternal report of last menstrual period\n* Intending to breastfeed and provide age-appropriate complementary feeding\n* Intend to continue services at the health center where they enrolled until their infant is at least 10 months old\n\nExclusion Criteria:\n\n* Women who participated in the formative phase of the HMHBT project\n* Women with an existing medical condition that merits precautions for a high-risk pregnancy and may affect study outcomes independently of the intervention. These include for example, uncontrolled or advanced diabetes, advanced kidney disease (stage 3 or higher); thyroid disease, autoimmune disorders such as lupus, moderate to severe rheumatoid arthritis, organ transplant; blood clotting or bleeding disorders, multiple sclerosis.\n* Women with a history of previous preterm delivery (\\\u003C32w) or very low birth weight babies (\\\u003C1.5kg)\n* Known history of serious obstetric complications that place the mother at increased risk for subsequent adverse events or complications. These include for example multiple miscarriages or stillbirths (\\>2); eclampsia, hemorrhage, placenta previa, placental abruption, uterine rupture\n* Women experiencing pregnancy loss, and neonatal or infant mortality will be excluded from further follow-up. Women who give birth to multiples will be retained but their data will be analyzed separately","35 Years",{"count":109,"type":21},594,[24],"The objective of the research is to test whether integrating a mother-baby nutrition toolkit into routine antenatal care service can improve maternal and infant nutrition in Amhara, Ethiopia",[30,113],"Child Nutrition",[115,116,117],"Healthy Mother Healthy Baby Toolkit","Maternal nutrition","Health Belief Model","RECRUITING","2025-03-20",{"date":121,"type":42},"2025-03-24",{"date":123,"type":42},"2024-11-27",{"date":125,"type":21},"2026-04",{"name":127,"class":49},"Emory University",2]