[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"sudden-infant-death\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:sudden-infant-death":24},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,39,92,125],{"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":4,"eligibilityCriteria":45,"healthyVolunteers":11,"sex":46,"minAge":47,"maxAge":4,"enrollmentInfo":48,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":50,"conditions":51,"keywords":70,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":91},"100345304","fetal-electrophysiologic-abnormalities-in-high-risk-pregnancies-associated-with-fetal-demise-100345304","NCT03775954","Fetal Electrophysiologic Abnormalities in High-Risk Pregnancies Associated With Fetal Demise","Fetal Electrophysiologic Abnormalities in High-risk Pregnancies Associated With Fetal Demise","Inclusion Criteria:\n\n* Current pregnancy complicated by one of the five diagnostic categories\n\n  * prior unexplained Stillbirth at\u002Fafter 20 weeks gestation\n  * fetal major congenital heart defect\n  * fetal hydrops\n  * fetal gastroschisis\n  * monochorionic twin pregnancy\n* Subject must be 18 years of age or older\n* Subject must be English speaking and must be able to read and sign the consent form in English\n* Subject must be able to recline comfortably for 1-3 hours\n* Subject must be willing to complete all three procedures (fMCG, fMCG, nECG) as per protocol, unless medically unable\n* Subject must be willing to allow us to review her and her infants prenatal, deliver, and post-natal records to verify diagnosis, and clinical findings.\n\nExclusion Criteria:\n\n* Severe claustrophobia not reduced by taking breaks, or by having the light on, or by having someone in the room with them.\n* Active labor\n* Acute illness\n* Unable to recline comfortably with a pillow for more than 1-3 hours (assuming some breaks are provided)\n* Weight over 450 lbs\n* An electric stimulation device (TENS unit, pacemaker, or nerve stimulator) that could produce electric or magnetic noise.\n\n  * Note that the Tristan 624 Magnetometer does not pose a risk to the subject's device, (since fMCG does not produce any energy or magnetism), but stimulators themselves can cause interference for our recordings. Some devices may still qualify, and discussion with study nurse may be useful if subject has a pacemaker or similar device.\n\nThe subject will have a single 2-3 hour fetal magnetocardiogram at approximately 20 and 27 weeks GA, and again, if medical condition allows, between 30 and 37 weeks GA, then her infant will have an ECG between 0 and 4 weeks of age. Subjects will be paid a nominal fee for their participation each time, as well as transportation reimbursement if \\>25 miles. For subjects traveling a long distance, the ECG may be performed locally or at home.","FEMALE","18 Years",{"count":49,"type":20},30,"Each year world-wide, 2.5 million fetuses die unexpectedly in the last half of pregnancy, 25,000 in the United States, making fetal demise ten-times more common than Sudden Infant Death Syndrome. This study will apply a novel type of non-invasive monitoring, called fetal magnetocardiography (fMCG) used thus far to successfully evaluate fetal arrhythmias, in order to discover potential hidden electrophysiologic abnormalities that could lead to fetal demise in five high-risk pregnancy conditions associated with fetal demise.",[52,53,54,55,56,57,58,59,60,61,24,62,63,64,65,66,67,68,69],"High Risk Pregnancy","Congenital Heart Disease","Fetal Hydrops","Twin Monochorionic Monoamniotic Placenta","Gastroschisis","Fetal Demise","Stillbirth","Fetal Arrhythmia","Long QT Syndrome","Intrauterine Fetal Death","Pregnancy Loss","Twin Twin Transfusion Syndrome","Birth Defect","Fetal Cardiac Anomaly","Fetal Cardiac Disorder","Fetal Death","Brugada Syndrome","Fetal Tachycardia",[71,58,72,73,74,52,75,76,77,78,79,80,81],"Fetal Magnetocardiography","Intrauterine Fetal Demise","Fetal Heart Rate Variability","Fetal Arrhythmias","Pregnancy","Fetal Anomaly","Fetal Echocardiography","Non-Stress Testing","New Technology","Birth Defects","Fetal Research","2026-03-02",{"date":84,"type":30},"2026-03-04",{"date":86,"type":30},"2018-07-01",{"date":88,"type":20},"2028-11-30",{"name":90,"class":37},"Medical College of Wisconsin",2,{"id":93,"slug":94,"hasResults":11,"nctId":95,"briefTitle":96,"officialTitle":97,"acronym":4,"eligibilityCriteria":98,"healthyVolunteers":99,"sex":17,"minAge":100,"maxAge":101,"enrollmentInfo":102,"targetDuration":4,"studyType":104,"phases":105,"briefSummary":107,"conditions":108,"keywords":109,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":115,"lastUpdatePostDateStruct":116,"startDateStruct":118,"completionDateStruct":120,"leadSponsor":122,"locationsCount":124},"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",true,"3 Days","75 Years",{"count":103,"type":20},350,"INTERVENTIONAL",[106],"NA","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],[110,111,112,113,114],"Counseling","Motivational Interviewing","Medical Informatics","Clinical Decision Support","Electronic Medical Record","2025-12-08",{"date":117,"type":30},"2025-12-09",{"date":119,"type":30},"2022-09-30",{"date":121,"type":20},"2027-02-28",{"name":123,"class":37},"Johns Hopkins University",1,{"id":126,"slug":127,"hasResults":11,"nctId":128,"briefTitle":129,"officialTitle":130,"acronym":131,"eligibilityCriteria":132,"healthyVolunteers":99,"sex":46,"minAge":4,"maxAge":4,"enrollmentInfo":133,"targetDuration":4,"studyType":104,"phases":135,"briefSummary":136,"conditions":137,"keywords":139,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":142,"lastUpdatePostDateStruct":143,"startDateStruct":145,"completionDateStruct":147,"leadSponsor":149,"locationsCount":124},"100563624","get-social-media-and-risk-reduction-training-100563624","NCT06618586","Get Social Media and Risk-Reduction Training","Get Social Media and Risk-Reduction Training (GET SMART)","GETSMART","Inclusion Criteria:\n\n* Must speak English or Spanish\n* Must live in the United States\n* Must have given birth to a healthy, term infants (37 weeks or greater) and be discharged within 7 days of birth\n* Must plan to care for infant and live in the same household as infant after birth\n* Must enroll in the TodaysBaby program by the time their infant is 7 days of age\n\nExclusion Criteria:\n\n* A prenatal diagnosis expected to have impact on infant care practices not compatible with study goals, such as supine infant sleep positioning.",{"count":134,"type":20},10000,[106],"This study examines the implementation of the TodaysBaby™ mobile safe sleep intervention program in US hospitals. The main aims of this study are to examine: 1) differences in program penetration and the equity of penetration according to income and race\u002Fethnicity; 2) differences in feasibility, acceptability, sustainability and fidelity top the intervention; and 3) the effectiveness of the intervention.",[138,24],"Infant Death",[140,141],"Safe Sleep","Mobile Messaging","2025-06-05",{"date":144,"type":30},"2025-06-11",{"date":146,"type":30},"2025-05-01",{"date":148,"type":20},"2028-06-01",{"name":150,"class":37},"University of Virginia"]