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Life sciences · Interventional Study
ClinicalTrials.gov · October 23, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Interventional Study.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
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Registry record from ClinicalTrials.gov (NCT07787845). This is a study registration, not published results. Lead sponsor: University of South Carolina. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 350 participants (ESTIMATED). Conditions: Doula Support, Postpartum, Postpartum Depression (PPD), Postpartum Anemia. Interventions: BEHAVIORAL: Doula-delivered, Nurse-coordinated postpartum support. Primary outcome measures: Rate of receipt of postpartum care within 2 weeks of delivery , From delivery of infant(s) to 2 weeks postpartum; Rate of receipt of postpartum care within 6 weeks of delivery , From delivery of infant(s) to 6 weeks postpartum. Brief summary: 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.