Sudden Infant Death

5

Review clinical trials related to Sudden Infant Death. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Improving Pediatrician Counseling About Infant Safe Sleep Using the Electronic Medical Record

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.

Participants needed: 350
Trial details
Age: 3-75Biological sex: AllType: InterventionalSponsor: Johns Hopkins UniversityUpdated: Jul 21, 2026Locations: 1
Eligibility criteria

English and Spanish-speaking parents and legal guardians bringing their infants... [+1]

Infant is considered medically complex (e.g., serious congenital anomaly, requir... [+1]

Status: Recruiting

Incorporation of Safe Sleep Education Into m-Health Technology

Sudden Unexplained Infant Death (SUID) is the leading cause of death in infants age 28 days to 1 year. Protective factors, such as supine positioning, firm sleep surface, breastfeeding, pacifier use, elimination of soft objects from the sleep space, and avoidance of tobacco, alcohol, and illicit drugs have been shown to decrease the risk. The American Academy of Pediatrics recommends that healthcare providers model and convey safe sleep practices during patient encounters. Pediatric emergency departments (PED) serve as front-line contact for populations at greatest risk for SUID, however few interventions have been tested in the PED setting. M- Health (mobile health) apps have previously demonstrated the ability to deliver safety education to parents and are well suited for use in the PED given limited clinician time and long wait times. Safety in Seconds (SIS) is a theory based, m-Health injury prevention tool focused on care seat safety and fire safety with previously demonstrated effectiveness in an NIH-funded randomized trial. This study aims to add safe sleep education into the SIS, and subsequently disseminate the app in the PED setting. Integration of safe sleep education into SIS represents an opportunity to increase safe sleep knowledge and practices through a proven effective m-Health intervention. This study addresses this potential by incorporating a previously developed, theory-driven and evidence-based safe sleep education into the SIS app and testing the feasibility of deployment in the PED.

Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Johns Hopkins UniversityUpdated: Jul 15, 2026Locations: 1
Eligibility criteria

English speaking caregivers over 18 of infants age 0-4 months [+1]

Non English speaking [+2]

Status: Recruiting

Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome

This is a multicenter genetic study aimed at identifying new genes/variants associated with sudden infant death syndrome (SIDS) based on whole-genome sequencing of family trios

Participants needed: 650
Trial details
Biological sex: AllType: ObservationalSponsor: Nantes University HospitalUpdated: Jun 18, 2026Locations: 18
Eligibility criteria

Child included in the French SUDI registry with effective participation in the b... [+4]

Presence of a known metabolic, genetic or syndromic pathology at the time of dea... [+2]

Status: Recruiting

Fetal Electrophysiologic Abnormalities in High-Risk Pregnancies Associated With Fetal Demise

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.

Participants needed: 30
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Medical College of WisconsinUpdated: Mar 4, 2026Locations: 2
Eligibility criteria

Current pregnancy complicated by one of the five diagnostic categories [+10]

Severe claustrophobia not reduced by taking breaks, or by having the light on, o... [+6]

Status: Recruiting

Get Social Media and Risk-Reduction Training

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/ethnicity; 2) differences in feasibility, acceptability, sustainability and fidelity top the intervention; and 3) the effectiveness of the intervention.

Participants needed: 10,000
Trial details
Biological sex: FemaleType: InterventionalSponsor: University of VirginiaUpdated: Jun 11, 2025Locations: 1
Eligibility criteria

Must speak English or Spanish [+4]

A prenatal diagnosis expected to have impact on infant care practices not compat...