[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"weight-gain-trajectory\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:weight-gain-trajectory":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,43,76,113],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":4},"100525913","learning-early-infant-feeding-cues-100525913",false,"NCT06127914","Learning Early Infant Feeding Cues","A Multiphase Project to Improve Use of Responsive Feeding Among Vulnerable Mother-Infant Dyads","LEIFc","Maternal Inclusion Criteria\n\n* Pregnant mother in the 3rd trimester (28 weeks or beyond)\n* Enrolled in a government-funded maternal-child home visiting program\n* Maternal age 18 years or older\n* English or Spanish speaking\n* Anticipated to have custody of infant after birth\n* Healthy pregnancy, no complications that are anticipated to result in a preterm birth or extended hospital stay for mother or infant\n\nMaternal Exclusion Criteria\n\n* Gave birth to multiple fetuses\n* Age less than 18 years\n* Not fluent in English or Spanish\n* Expected to not have custody of the infant after birth\n\nInfant inclusion criteria\n\n* Born as a singleton (not a twin, triplet, etc.) to a mother enrolled in a maternal-child home visiting program\n* Born full term (37 weeks or beyond)\n\nInfant exclusion criteria\n\n* Congenital anomaly that may interfere with infant feeding or growth after birth (i.e., Down Syndrome, cleft lip\u002Fpalate)\n* Born preterm (born prior to 37 weeks)\n* NICU stay beyond 48 hours\n* Infant diagnosis of failure to thrive\n* Supplemental oxygen\n* Enteral feeding device used for feedings",true,"FEMALE","2 Weeks",{"count":21,"type":22},39,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this clinical trial is to learn more about responsive infant feeding (recognizing baby's signs of hunger and fullness) in mothers and infant enrolled in government-funded maternal-child home visiting programs. The main questions it aims to answer are:\n\n* What are the contributors and barriers to use of responsive infant feeding?\n* How can we refine an intervention focused on responsive infant feeding (the Learning Early Infant Feeding Cues intervention) so that mothers will like it and learn skills to help their baby be healthy.\n* Will the refined intervention improve use of responsive feeding and be feasible and acceptable to mothers and home visiting programs?\n\nParticipants will be asked to:\n\n* Participate in focus groups to talk about their experiences feeding their baby.\n* Participate in a study to learn about responsive feeding and how to use it with their baby. This study will start when mothers are in their final month of pregnancy and finish when their baby is 6 months old. Participation will include:\n\n  * Having someone come to the family home during a time when the baby is eating (either from the breast or the bottle). The mother will receive information on the baby's signs from an experienced coach.\n  * Agreeing to be video recording during the session when the baby is eating.\n  * Completing surveys online.",[28,29,30],"Responsive Feeding","Infants","Weight Gain Trajectory","NOT_YET_RECRUITING","2026-04-22",{"date":34,"type":35},"2026-04-27","ACTUAL",{"date":37,"type":22},"2027-07-01",{"date":39,"type":22},"2029-06-30",{"name":41,"class":42},"Florida State University","OTHER",{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":17,"sex":51,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":23,"phases":56,"briefSummary":57,"conditions":58,"keywords":63,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":75},"100630932","evaluating-care-integration-between-pediatric-primary-care-providers-and-wic-nutritionists-100630932","NCT07494097","Evaluating Care Integration Between Pediatric Primary Care Providers and WIC Nutritionists","Evaluating Care Integration Between Pediatric Primary Care Providers and WIC Nutritionists for Early Obesity Prevention Among WIC Mothers and Children","WEE Baby","Inclusion Criteria:\n\n* People who are a) pregnant and \\>34 weeks' gestation or b) who have an infant \\\u003C2 months old\n* 18-40 years old\n* English and\u002For Spanish speaking and reading\n* Access to a smartphone or internet-connected device\n* Not planning to move out of Pennsylvania within 2 years\n* Not planning to change health care providers outside of Geisinger within 2 years\n* Custody of and lives with (or will live with) the child enrolled in the study\n* Child must have a Geisinger PCP and be a WIC participant or eligible for WIC at enrollment\n\nExclusion Criteria:\n\n* Mother is not interested (or willing) to enroll in WIC\n* Child has a genetic or developmental disorder (e.g., cleft palate) that impacts weight or feeding\n* Child has a terminal condition","ALL","18 Years","40 Years",{"count":55,"type":22},380,[25],"This study looks at whether using secure digital systems to share information between pediatric health care providers (during regular well-child visits) and social care providers (during regular visits with WIC nutritionists) can help mothers receive consistent guidance on responsive parenting to support healthy child growth and development. Responsive parenting means learning how to respond to a baby's needs in ways that support healthy eating, sleep, activity, and emotion regulation habits. The main questions this study aims to answer are:\n\n1. Does using secure digital systems to share information between pediatric health care providers and social care providers help mothers receive consistent guidance on responsive parenting to support healthy growth from birth to 24 months?\n2. Does using secure digital systems to share information between pediatric health care providers and social care providers help mothers receive consistent guidance on responsive parenting, improve responsive parenting practices and child diet quality?\n\nThe investigators will compare the group that receives secure digital systems for sharing information on responsive parenting to a group that receives standard care (does not receive this) to see if secure digital systems for sharing information on responsive parenting work to support healthy child growth and development. The goal is to see if this approach can improve early health behaviors and reduce health disparities for families in rural, low-income communities.",[30,59,60,61,62],"BMI","Responsive Parenting","Diet Quality","Implementation",[64,60,65],"Child Weight","Health Information Technologies","2026-03-19",{"date":68,"type":35},"2026-03-27",{"date":70,"type":22},"2026-08",{"date":72,"type":22},"2029-12",{"name":74,"class":42},"Penn State University",1,{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":82,"eligibilityCriteria":83,"healthyVolunteers":17,"sex":51,"minAge":84,"maxAge":4,"enrollmentInfo":85,"targetDuration":4,"studyType":23,"phases":87,"briefSummary":89,"conditions":90,"keywords":94,"overallStatus":103,"whyStopped":4,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":75},"100518251","phase-2-a-novel-obesity-prevention-program-for-high-risk-infants-in-primary-care-100518251","NCT06028113","A Novel Obesity Prevention Program for High-Risk Infants in Primary Care","A Novel Obesity Prevention Program for High-Risk Infants in Pediatric Primary Care: The THRIVE Randomized Controlled Trial","THRIVE","Inclusion Criteria:\n\n* born 2500 grams or greater\n* delivery occurring between 37 and 42 weeks gestation\n* English speaking\n* infant receiving care provided at our pediatric primary care setting\n* from a racial \u002F ethnic minority group (i.e., non-white, or Hispanic or Latinx) and\u002For economically marginalized background (i.e., household income at or below 138% of federal poverty level; qualifying for Medicaid)\n\nExclusion Criteria:\n\n* care in the Neonatal Intensive Care Unit (\\>7 days)\n* infant congenital anomaly or neonatal condition that affects feeding (e.g., cleft lip\u002Fpalate, metabolic disease)\n* infant exposure to illicit drugs in utero \\[with the exception of tetrahydrocannabinol (THC)\\]\n* diminished or impaired caregiver cognitive functioning\n* family intent to move from the area within 1 year","1 Day",{"count":86,"type":22},144,[88],"PHASE2","The goal of this clinical trial is to test a responsive parenting obesity prevention program with infants and caregivers of color (e.g., non-White; Hispanic\u002FLatinx) and\u002For who are economically marginalized (i.e., publicly insured), delivered via Integrated Behavioral Health (IBH) in pediatric primary care. The main questions it aims to answer are:\n\n* 1\\) Is the obesity prevention intervention delivered via IBH in pediatric primary care feasible and acceptable to families of color and\u002For families who are economically marginalized?\n* 2\\) Will it prevent rapid weight gain during infancy?\n\nParticipants will complete baseline (newborn), post-treatment (9 months), and follow-up assessments (12 months). Participants assigned to treatment will receive 4 prevention sessions as part of their typical well-child visit in pediatric primary care. Researchers hypothesize that infants in the obesity prevention intervention will have stable weight gain compared to infants in the control group (treatment as usual) will experience more rapid weight gain.",[91,92,93,30],"Obesity","Obesity, Childhood","Weight Gain",[95,96,97,98,99,100,101,102],"obesity prevention","infancy","integrated primary care","integrated behavioral health","responsive parenting","responsive feeding","sleep","soothing","RECRUITING","2025-03-03",{"date":106,"type":35},"2025-03-05",{"date":108,"type":35},"2023-10-05",{"date":110,"type":22},"2026-01-30",{"name":112,"class":42},"Children's Hospital Medical Center, Cincinnati",{"id":114,"slug":115,"hasResults":11,"nctId":116,"briefTitle":117,"officialTitle":118,"acronym":4,"eligibilityCriteria":119,"healthyVolunteers":17,"sex":18,"minAge":52,"maxAge":120,"enrollmentInfo":121,"targetDuration":4,"studyType":23,"phases":123,"briefSummary":124,"conditions":125,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":128,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":134,"locationsCount":75},"100532830","effects-of-monitoring-blood-pressure-during-pregnancy-100532830","NCT06217913","Effects of Monitoring Blood Pressure During Pregnancy","Effects of Monitoring Blood Pressure in High-risk Pregnant Women Using a Wearable Device","Inclusion Criteria:\n\n* Women with a single pregnancy before 12 weeks of pregnancy\n* The presence of any of the following risk factors: age \\> 30 years, a history of eclampsia, a family history of eclampsia, obesity (BMI ≥ 30 Kg\u002Fm2), and a history of gestational hyperglycemia (pregestational type 1 and type 2 diabetes; gestational manifest diabetes and gestational diabetes requiring insulin treatment), preexisting chronic hypertension, kidney disease, and autoimmune diseases such as systemic lupus erythematosus and antiphospholipid syndrome.\n* Signed the informed consent can be continuously followed up.\n* Permanent population living in the study area.\n* All subjects received routine antenatal examination and treatment.\n\nExclusion Criteria:\n\n* Termination of pregnancy before 20 weeks\n* Withdraw from the study\n* Lost visitors","60 Years",{"count":122,"type":22},400,[25],"In this study, at least 400 women with high-risk of pregnancy hypertension will use a wearable device to monitor the blood pressure during gestational age from 12 weeks to 28weeks. The observed outcomes including maternal and offspring. Participants were from three hospital including Shanghai Xinhua Hospital, Jiaxing Maternal and Child Health Hospital and Peking University Third Hospital. Pregnant women were randomly divided into control group (routine delivery examination group) and intervention group (routine delivery examination group + use of wearable blood pressure monitoring device group), 200 cases each.",[126,30],"Birth Weight","2024-01-11",{"date":129,"type":35},"2024-01-23",{"date":131,"type":22},"2024-12-01",{"date":133,"type":22},"2027-06-30",{"name":135,"class":42},"Xinhua Hospital, Shanghai Jiao Tong University School of Medicine"]