[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"sudden-unexplained-infant-death\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:sudden-unexplained-infant-death":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,39,110],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":27,"lastUpdatePostDateStruct":28,"startDateStruct":31,"completionDateStruct":33,"leadSponsor":35,"locationsCount":38},"100534869","identification-of-genetic-variants-associated-with-unexpected-infant-death-syndrome-100534869",false,"NCT06244433","Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome","Risk Stratification of Sudden Unexpected Death in Infant Based on Biomarkers - Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome","BIOMINRISK","Child Inclusion Criteria\n\n* Death of a child between 0 and 2 years of age due to sudden unexpected death in infant\n* Child included in the French SUDI registry with effective participation in the biocollection\n* Children who also meet the inclusion criteria for the BIOMINRISK-NEUROBIO (axis 2) and BIOMINRISK-RADIO-ANAT (axis 3) studies in the overall BIOMINRISK project.\n\nParents Inclusion Criteria\n\n* Biological parents of the child included in the BIOMINRISK study\n* Parents who have both signed the consent form for blood collection and inclusion of their samples in the biocollection\n* parents beneficiaries of a social security or similar scheme\n\nChild Exclusion Criteria:\n\n* Presence of a known metabolic, genetic or syndromic pathology at the time of death\n\nParents Exclusion Crtiteria:\n\n* Parent under guardianship\n* Presence of a known metabolic, genetic or syndromic pathology","ALL",{"count":19,"type":20},650,"ESTIMATED","OBSERVATIONAL","This is a multicenter genetic study aimed at identifying new genes\u002Fvariants associated with sudden infant death syndrome (SIDS) based on whole-genome sequencing of family trios",[24,25],"Sudden Infant Death","Sudden Unexplained Infant Death","RECRUITING","2026-06-16",{"date":29,"type":30},"2026-06-18","ACTUAL",{"date":32,"type":30},"2024-08-27",{"date":34,"type":20},"2027-10-27",{"name":36,"class":37},"Nantes University Hospital","OTHER",18,{"id":40,"slug":41,"hasResults":11,"nctId":42,"briefTitle":43,"officialTitle":44,"acronym":45,"eligibilityCriteria":46,"healthyVolunteers":47,"sex":17,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":52,"phases":53,"briefSummary":55,"conditions":56,"keywords":73,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":109},"100569405","advanced-wireless-sensors-for-neonatal-care-in-the-delivery-room-100569405","NCT06693817","Advanced Wireless Sensors for Neonatal Care in the Delivery Room","Advanced Wireless Sensors for Neonatal Care in the Delivery Room: the AWARD Prospective Multicenter International Study","AWARD","Inclusion criteria:\n\n1. Newborns ≥35 weeks (gestational age)\n2. Newborns determined to be clinically stable at delivery\n3. Newborns with no skin abnormalities\n\nExclusion criteria:\n\n1. Newborns ≤ 35 weeks (gestational age)\n2. Newborns determined to not be clinically stable at delivery\n3. Newborns with Skin abnormalities",true,"35 Weeks","42 Weeks",{"count":51,"type":20},600,"INTERVENTIONAL",[54],"NA","The goals of this observational study is to assess whether a new advanced wireless skin sensor vital sign monitoring system can effectively monitor the vital signs of healthy newborn infants (≥ 35 weeks gestational age). The main aims of this Study are to:\n\n1. Assess feasibility\n2. Evaluate safety\n3. Determine accuracy of the wireless monitoring system, compared to the standard of care wired vital sign monitoring system, immediately after delivery and for the first 2h of age in the obstetrical center under unsupervised parents' care. The newborn infants participating in the Study will have both vital sign monitoring systems placed on their chest and limb. Their vital signs will be monitored for 2h consecutively.",[25,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72],"Apnea of Newborn","Newborn Morbidity","Newborn Asphyxia","Birth Outcome, Adverse","Birth Asphyxia","Pregnancy Related","Newborn; Vitality","ECG Electrode Site Reaction","Infant ALL","Infant Death","Infant, Newborn, Diseases","Infant Apnea","Infant Conditions","Parents","Delivery Problem for Fetus","Delivery Complication",[74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99],"Delivery Room","Newborn","Neonatal Resuscitation","Wireless Technology","Vital Sign Monitoring","Sudden Unexplained Post-Natal Collapse","SUPC","Obstetrical Center","Obstetrics","Neonate","Birth","Birthing Center","C-Section","Vaginal Delivery","Sensors","Heart Rate (HR)","Respiratory Rate (RR)","Blood Oxygen Saturation (SpO2)","Skin Temperature (Tskin)","Pulse Rate (PR)","International","Low-Income","Middle-Income","High-Income","Golden Hour","Post-Birth","2026-05-05",{"date":102,"type":30},"2026-05-08",{"date":104,"type":30},"2025-04-08",{"date":106,"type":20},"2027-12-30",{"name":108,"class":37},"Guilherme Sant'Anna, MD",5,{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":115,"acronym":4,"eligibilityCriteria":116,"healthyVolunteers":47,"sex":17,"minAge":117,"maxAge":118,"enrollmentInfo":119,"targetDuration":4,"studyType":52,"phases":121,"briefSummary":122,"conditions":123,"keywords":124,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":130,"lastUpdatePostDateStruct":131,"startDateStruct":133,"completionDateStruct":135,"leadSponsor":137,"locationsCount":139},"100477961","improving-pediatrician-counseling-about-infant-safe-sleep-using-the-electronic-medical-record-100477961","NCT05503771","Improving Pediatrician Counseling About Infant Safe Sleep Using the Electronic Medical Record","Health IT to Reduce Disparities in Risks for Sleep-related Infant Deaths, (SAFE Start 2.0 Project)","Inclusion Criteria:\n\n* English and Spanish-speaking parents and legal guardians bringing their infants to the Harriet Lane Clinic (pediatric primary care clinic) for any of their early well baby visits (between 3-5 days up to 4 weeks of age)\n* Maryland recognizes teen parents as emancipated minors, so they will be eligible to provide consent and participate.\n\nExclusion Criteria:\n\n* Infant is considered medically complex (e.g., serious congenital anomaly, requires cardiorespiratory monitoring, etc.)\n* Assigned resident is not enrolled in the study","3 Days","75 Years",{"count":120,"type":20},350,[54],"The study team will evaluate the impact of an Infant Sleep Assessment (ISA) tool with motivational interviewing (MI) communication training on clinician-parent communication during 2-month Well Baby Visits (WBV) and parent reported and observed infant sleep practices. The study team's hypotheses are that 1) clinicians who utilize the ISA with MI training will more effectively communicate safe sleep information to their patients' parents, and 2) these parents will have safer infant sleep practices than parents whose clinicians are in a standard of care control group.",[24,25],[125,126,127,128,129],"Counseling","Motivational Interviewing","Medical Informatics","Clinical Decision Support","Electronic Medical Record","2025-12-08",{"date":132,"type":30},"2025-12-09",{"date":134,"type":30},"2022-09-30",{"date":136,"type":20},"2027-02-28",{"name":138,"class":37},"Johns Hopkins University",1]