[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"infant-death\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:infant-death":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,45,114,144,175,201,223,236,260],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":5},"100054167","comparative-outcomes-related-to-delivery-room-cord-milking-in-low-resourced-kountries--preterm-100054167",false,"NCT06240715","Comparative Outcomes Related to Delivery-room Cord Milking In Low-resourced Kountries- PreTerm","A Cluster Randomized Clinical Trial of Umbilical Cord Milking Compared to Early Cord Clamping in Preterm Infants Who Are Non-vigorous at Birth","CORDMILK-PT","Inclusion Criteria:\n\n* Preterm infants born between 30 0\u002F7 weeks to 34 6\u002F7 weeks of gestation\n* Non-vigorous at birth\n\nExclusion Criteria:\n\n* Infants with congenital malformation\n* Major chromosomal abnormalities\n* Complete placental abruption\u002Fcutting through the placenta at the time of delivery\n* Cord conditions (umbilical knots, inadequate cord length, cord rupture, non-reducible nuchal cord)\n* Mono-chorionic twins,\n* Twins with no information on amnion\u002Fchorion\n* Multiple gestation \\>2","ALL","0 Minutes","10 Minutes",{"count":21,"type":22},800,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this multicenter, cluster-randomized, crossover trial is to determine if umbilical cord milking compared to early cord clamping will reduce in-hospital mortality in non-vigorous preterm infants born between 30 weeks and 34 weeks of gestation.",[28,29],"Preterm","Infant Death",[28,31,32],"Umbilical cord milking","Placental transfusion","RECRUITING","2026-07-09",{"date":36,"type":37},"2026-07-13","ACTUAL",{"date":39,"type":37},"2024-07-01",{"date":41,"type":22},"2027-03-30",{"name":43,"class":44},"Nemours Children's Clinic","OTHER",{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":53,"sex":17,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":23,"phases":58,"briefSummary":59,"conditions":60,"keywords":77,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":113},"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":57,"type":22},600,[25],"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.",[61,62,63,64,65,66,67,68,69,70,29,71,72,73,74,75,76],"Sudden Unexplained Infant Death","Apnea of Newborn","Newborn Morbidity","Newborn Asphyxia","Birth Outcome, Adverse","Birth Asphyxia","Pregnancy Related","Newborn; Vitality","ECG Electrode Site Reaction","Infant ALL","Infant, Newborn, Diseases","Infant Apnea","Infant Conditions","Parents","Delivery Problem for Fetus","Delivery Complication",[78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103],"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":106,"type":37},"2026-05-08",{"date":108,"type":37},"2025-04-08",{"date":110,"type":22},"2027-12-30",{"name":112,"class":44},"Guilherme Sant'Anna, MD",5,{"id":115,"slug":116,"hasResults":11,"nctId":117,"briefTitle":118,"officialTitle":118,"acronym":119,"eligibilityCriteria":120,"healthyVolunteers":53,"sex":17,"minAge":121,"maxAge":4,"enrollmentInfo":122,"targetDuration":4,"studyType":23,"phases":124,"briefSummary":125,"conditions":126,"keywords":4,"overallStatus":132,"whyStopped":4,"lastUpdateSubmitDate":133,"lastUpdatePostDateStruct":134,"startDateStruct":136,"completionDateStruct":138,"leadSponsor":140,"locationsCount":143},"100593861","walk-with-me-wwm-for-perinatal-grief-100593861","NCT07011940","Walk With Me (WWM) for Perinatal Grief","PeriGrief-II","Inclusion Criteria:\n\n* Within the first month of pregnancy or early infant loss\n* Reside in the United State\n* Speak and read either English or Spanish at a 6th grade reading level\n* 15 or older\n\nExclusion Criteria:\n\n* Not pregnant or has not experienced an early infant loss\n* Does not reside in the United State\n* Does not speak and read either English or Spanish at a 6th grade reading level\n* 14 or younger","15 Years",{"count":123,"type":22},300,[25],"The goal of this clinical trial is to learn if the Along With Me web-based intervention works to decrease posttraumatic stress symptoms and suicidal ideation among bereaved parents following pregnancy and early infant loss. It will also learn whether peer guides provide additional improvements on these outcomes.\n\nThe main questions it aims to answer are:\n\n• Do people who receive Along With Me or Along With Me plus a Peer Guide compared to services as usual have lower posttraumatic stress symptoms and suicidal ideation than those who do not receive the intervention?\n\nResearchers will compare Along With Me and Along With Me plus a Peer Guide to services as usual (referrals made in the hospital setting) to see if Along With Me works to prevent and address posttraumatic stress symptoms and suicidal ideation.\n\nParticipants will:\n\n* Receive access to a mobile app with approximately 10 therapeutic modules about how to manage grief and other symptoms.\n* Receive check-ins with a Peer Guide (in the Peer Guide condition only)",[127,128,129,130,131,29],"Grief","Post Traumatic Stress Disorder","Suicidal Ideation","Miscarriage","Stillbirth","NOT_YET_RECRUITING","2026-03-04",{"date":135,"type":37},"2026-03-06",{"date":137,"type":22},"2026-07-01",{"date":139,"type":22},"2027-08-31",{"name":141,"class":142},"Oregon Research Behavioral Intervention Strategies, Inc.","INDUSTRY",1,{"id":145,"slug":146,"hasResults":11,"nctId":147,"briefTitle":148,"officialTitle":148,"acronym":149,"eligibilityCriteria":150,"healthyVolunteers":53,"sex":151,"minAge":4,"maxAge":4,"enrollmentInfo":152,"targetDuration":4,"studyType":23,"phases":154,"briefSummary":155,"conditions":156,"keywords":160,"overallStatus":132,"whyStopped":4,"lastUpdateSubmitDate":166,"lastUpdatePostDateStruct":167,"startDateStruct":169,"completionDateStruct":171,"leadSponsor":173,"locationsCount":143},"100619581","determining-the-effect-of-midwife-led-safe-infant-care-training-for-pregnant-women-on-awareness-of-sudden-infant-death-syndrome-and-home-accidents-100619581","NCT07346482","Determining the Effect of Midwife-Led Safe Infant Care Training for Pregnant Women on Awareness of Sudden Infant Death Syndrome and Home Accidents","Infant Care","Inclusion Criteria:\n\n* Volunteering to participate in the research\n* Being able to speak and understand Turkish\n* Being literate\n* Being a primiparous pregnant woman (due to the greater need for information) ≥36th week of pregnancy (because it is close to delivery and there is sufficient time to translate what they have learned into behavior)\n\nExclusion Criteria:\n\n* Diagnosed high-risk pregnancy\n* Diagnosed mental health condition\n* Having previously received training\u002Fcourse in safe infant care","FEMALE",{"count":153,"type":22},120,[25],"This project is a pioneering study in determining the impact of midwife-led safe infant care training for pregnant women on awareness of sudden infant death syndrome (SIDS) and home accidents. Raising awareness and improving women's knowledge about SIDS and home accidents is expected to help reduce preventable infant deaths. If the effectiveness of this training is proven, integrating it into prenatal care programs would be a significant step towards improving maternal and child health.",[29,149,157,158,159],"Midwifery","Education","Accident at Home",[161,162,163,164,165],"infant","infant death","midwifery care","accident","education","2026-01-16",{"date":168,"type":37},"2026-01-20",{"date":170,"type":22},"2026-02-16",{"date":172,"type":22},"2027-01-20",{"name":174,"class":44},"Cukurova University",{"id":176,"slug":177,"hasResults":11,"nctId":178,"briefTitle":179,"officialTitle":180,"acronym":181,"eligibilityCriteria":182,"healthyVolunteers":11,"sex":151,"minAge":4,"maxAge":4,"enrollmentInfo":183,"targetDuration":4,"studyType":23,"phases":185,"briefSummary":186,"conditions":187,"keywords":190,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":193,"lastUpdatePostDateStruct":194,"startDateStruct":196,"completionDateStruct":198,"leadSponsor":199,"locationsCount":143},"100498238","support-via-online-social-networks-to-promote-safe-infant-care-practices-100498238","NCT05767658","Support Via Online Social Networks to Promote Safe Infant Care Practices","Support Via Online Social Networks to Promote Safe Infant Care Practices Toward Reducing Racial Disparities in Infant Mortality","SUPERSONIC","Inclusion Criteria:\n\n* Currently enrolled in WIC, or it not, then have either Medicaid or no health insurance\n* Must be English speaking\n* Must be pregnant and less than 30 weeks gestation\n* Must live in the United States\n* Must have regular access to Facebook and short message service (SMS) texting (mobile phone)\n\nExclusion Criteria:\n\n* Not planning to live in same home as infant after birth.\n* Prenatal diagnosis expected to impact on infant care practices in a manner not compatible with study goals, including contraindications to feeding any breastmilk or supine infant sleep positioning.\n* Known or reported mental health or other issues that would preclude custody of the infant or being able to participate in the informed consent process.\n* Meets the definition of a minor according to applicable state law.\n* Participants who consent to participation in the study, must complete the Agile Onboarding process before they reach 30+0 weeks gestation.\n* Currently or previously received a TodaysBaby educational program (randomized to a TodaysBaby program through either the SMARTER, or SUPERSONIC study), either in their current or a previous pregnancy.",{"count":184,"type":22},3000,[25],"This study aims to improve adherence to American Academy of Pediatrics safe sleep (SS) recommendations and improve rates of initiation and duration of partial and exclusive breastfeeding (BF); and reduce Black\u002FWhite disparities in these practices through the use of private Facebook groups providing a) evidence-based education through videos and other multi-media supporting best practices and b) an online community and social network of other pregnant WIC clients and new parents.",[188,29,189],"Breastfeeding","Sudden Infant Death Syndrome Without Mention of Autopsy",[191,188,192],"Safe Sleep","Social Media","2026-01-09",{"date":195,"type":37},"2026-01-12",{"date":197,"type":37},"2024-03-01",{"date":137,"type":22},{"name":200,"class":44},"University of Virginia",{"id":202,"slug":203,"hasResults":11,"nctId":204,"briefTitle":205,"officialTitle":205,"acronym":4,"eligibilityCriteria":206,"healthyVolunteers":53,"sex":17,"minAge":207,"maxAge":4,"enrollmentInfo":208,"targetDuration":4,"studyType":210,"phases":4,"briefSummary":211,"conditions":212,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":214,"lastUpdatePostDateStruct":215,"startDateStruct":217,"completionDateStruct":219,"leadSponsor":221,"locationsCount":143},"100543856","the-happiest-baby-inc-snoo-postmarket-surveillance-study-100543856","NCT06361303","The Happiest Baby, Inc. SNOO Postmarket Surveillance Study","Inclusion Criteria:\n\nInfant\u002Fcaregiver dyads meeting the following inclusion criteria will be eligible for study enrollment:\n\n* Respondent must identify as a primary caregiver of the infant.\n* Purchase or rental of SNOO shipped to a U.S. residence during the defined enrollment period.\n* Caregivers must be English speakers ages 18 or older residing in the United States.\n* Infants must use SNOO during the intended use period (i.e., birth to 6 months).\n* Infants must meet at least one of the following criteria for high risk for SUID:\n\n  * Infant race: Black or African American; and\u002For American Indian or Alaskan Native\n  * Maternal education: 12 years or less\n  * Low birth weight: \\\u003C5 pounds 8 ounces (\\\u003C2500 grams)\n  * Last menstrual cycle (LMP) or obstetrical estimate (OE) Gestational age at time of birth: \\\u003C37 weeks (preterm)\n  * Maternal age at time of birth: \\\u003C25 years\n  * Smoking status: Any self-reported maternal smoking during pregnancy\n\nExclusion Criteria:\n\n* Not primary caregiver\n* Does not speak English\n* Is not a US resident\n* Is not 18 years old or older\n* Infant did not use SNOO during the intended use period (i.e., birth to 6 months).\n* Infants does NOT meet at least one of the below risk criteria:\n\n  * Infant race: Black or African American; and\u002For American Indian or Alaskan Native\n  * Maternal education: 12 years or less\n  * Low birth weight: \\\u003C5 pounds 8 ounces (\\\u003C2500 grams)\n  * LMP or OE Gestational age at time of birth: \\\u003C37 weeks (preterm)\n  * Maternal age at time of birth: \\\u003C25 years\n  * Smoking status: Any self-reported maternal smoking during pregnancy","18 Years",{"count":209,"type":22},1000,"OBSERVATIONAL","This postmarket surveillance study will evaluate the safety of the SNOO Smart Sleeper Bassinet when used for infants who are at high risk for Sudden Unexpected Infant Death (SUID). This study will survey 1000 caregivers of high-risk infants to examine the frequency of death or serious injury occurring in the SNOO Bassinet.",[29,213],"Serious Injury","2025-09-04",{"date":216,"type":37},"2025-09-05",{"date":218,"type":37},"2023-11-29",{"date":220,"type":22},"2026-05",{"name":222,"class":142},"Happiest Baby, Inc.",{"id":224,"slug":4,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":225,"targetDuration":4,"studyType":23,"phases":226,"briefSummary":26,"conditions":227,"keywords":228,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":229,"lastUpdatePostDateStruct":230,"startDateStruct":232,"completionDateStruct":233,"leadSponsor":235,"locationsCount":5},"100534583",{"count":21,"type":22},[25],[28,29],[28,31,32],"2025-07-08",{"date":231,"type":37},"2025-07-11",{"date":39,"type":37},{"date":234,"type":22},"2026-12-30",{"name":43,"class":44},{"id":237,"slug":238,"hasResults":11,"nctId":239,"briefTitle":240,"officialTitle":241,"acronym":242,"eligibilityCriteria":243,"healthyVolunteers":53,"sex":151,"minAge":4,"maxAge":4,"enrollmentInfo":244,"targetDuration":4,"studyType":23,"phases":246,"briefSummary":247,"conditions":248,"keywords":250,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":252,"lastUpdatePostDateStruct":253,"startDateStruct":255,"completionDateStruct":257,"leadSponsor":259,"locationsCount":143},"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":245,"type":22},10000,[25],"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.",[29,249],"Sudden Infant Death",[191,251],"Mobile Messaging","2025-06-05",{"date":254,"type":37},"2025-06-11",{"date":256,"type":37},"2025-05-01",{"date":258,"type":22},"2028-06-01",{"name":200,"class":44},{"id":261,"slug":262,"hasResults":11,"nctId":263,"briefTitle":264,"officialTitle":264,"acronym":265,"eligibilityCriteria":266,"healthyVolunteers":11,"sex":151,"minAge":207,"maxAge":4,"enrollmentInfo":267,"targetDuration":4,"studyType":210,"phases":4,"briefSummary":269,"conditions":270,"keywords":274,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":279,"lastUpdatePostDateStruct":280,"startDateStruct":282,"completionDateStruct":284,"leadSponsor":286,"locationsCount":288},"100536644","increasing-neonatal-hiv-test-and-treat-to-maximize-the-long-term-impact-on-infant-health-and-novel-infant-antiretroviral-treatment-100536644","NCT06267508","Increasing Neonatal HIV Test and Treat to Maximize the Long-Term Impact on Infant Health and Novel Infant Antiretroviral Treatment","LIFE2Scale","Inclusion Criteria:\n\n1. Voluntary and informed consent of the mother for her own study participation (if applicable);\n2. Voluntary and informed consent of the legal guardian of the child for participation of the child in the study;\n3. Mothers\u002Flegal guardians ≥18 years of age;\n4. Documented maternal HIV infection;\n5. Willingness to consent to HIV testing for the child and herself (or just her child); and\n6. Willingness to consent to active tracing including home tracing.\n\n   Exclusion Criteria:\n7. Deficiency in the mother, rendering it difficult, if not impossible, for her or her infant to take part in the study or understand the information provided to her.\n8. Having delivered more than 72h (3 days) ago;\n9. Prisoners;\n10. Women presenting with an emergency requiring immediate medical assistance if not resolved at study inclusion;\n11. Stillbirths;\n12. Infant requiring emergency care (e.g. immediate or rapid occurring life threatening conditions, resuscitation, prolonged obstetric related intensive care, severe jaundice) or born with severe malformation;\n13. If within the discretion of the investigator based on recommendation of the gynaecologist or paediatrician in charge study participation would possibly add not acceptable risk or burden to the mother or infant (e.g. significant congenital malformation, health deficiencies, very low birth weight less than 1500g); or\n14. Unlikely to comply with protocol as judged by the principal investigator or his designate",{"count":268,"type":22},6000,"This study aims to improve HIV healthcare services for mothers living with HIV and their newborns in Tanzania and Mozambique. The main questions it aims to answer are: 1) does enhancing screening with maternal HIV viral load monitoring at delivery identify more mother-child pairs at high-risk for HIV vertical transmission? and 2) are high-risk infants linked to appropriate prevention and care? The study will expand access to HIV testing services to more rural settings using a hub-and-spoke referral system.",[271,272,29,273,71],"Vertical Human Immunodeficiency Virus Transmission","HIV Infection Pediatric","Infant Morbidity",[275,276,277,278],"Prevention of Vertical HIV Transmission (PVHT)","Infant HIV Prophylaxis","Early Infant HIV Diagnosis","Infant Antiretroviral Treatment","2024-11-14",{"date":281,"type":37},"2024-11-18",{"date":283,"type":37},"2024-04-30",{"date":285,"type":22},"2025-12",{"name":287,"class":44},"Michael Hoelscher",2]