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The Goal is to Examine the Impact of Doula-delivered, Nurse-coordinated Postpartum Care Among Individuals With Preterm Births <34 Weeks' Gestation Requiring NICU Admission.

RecruitingNAAges 18 Years - anyFemaleUniversity of South Carolina
NCT07787845 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The primary objective of this research is to conduct a randomized clinical trial to examine the impact of nurse-coordinated, doula-delivered postpartum support (intervention arm) on postpartum health care utilization, health outcomes, and patient-reported experiences compared with standard postpartum care (control arm) among individuals with preterm births \<34 weeks' gestation requiring neonatal intensive care unit (NICU) admission.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Age above 18 at time of delivery of infant * English-speaking * Medicaid insurance coverage at the time of delivery, either as primary or secondary coverage * Delivery before 34 weeks' gestation * Infant admitted to the NICU, 10 days old or less Exclusion Criteria: * Stillbirth * Infant death in the delivery room * Infant with severe congenital anomalies expected to result in death shortly after birth * Inability to provide informed consent * Inability to visit the infant in the NICU at least once per week * More than 10 days postpartum
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What it tests

  • Doula-delivered, Nurse-coordinated postpartum support
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Where

1 site
Prisma Health Richland
Columbia, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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