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Evaluation of a Health System Integrated Model for Postpartum Education and Support in Rural Populations

Study acronym: NEST-Rural
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 3 months later Jun 2027 → Oct 2027
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Record History

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  1. Primary endpoints: details revised at 1 of 11 entries Show 5 more changesShow less
    • Primary completion pushed from Jun 2027 to Oct 2027
    • Study completion moved earlier from Dec 2029 to Oct 2029
    • Eligibility criteria expanded, about 6 words
    • Secondary endpoints: details revised at 2 of 17 entries
    • Study description revised
  2. Site contact updatedv5
  3. Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Start date changed from estimate of Dec 2024 to Dec 4, 2024
    v4
  4. Re-verified, no change to tracked fieldsv3
  5. Start date: Nov 2024 to Dec 2024v2
  6. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This study was designed to evaluate the implementation of the Nurse Education and Support Team (NEST) Program for postpartum women who reside in 5 rural counties in North Carolina. Overarching Hypothesis: Mothers and infants residing in rural communities, randomized to the NEST-Rural care model over the 3-year course of the project will: 1. Receive more coordinated care for addressing social, mental and physical health needs. 2. Experience fewer postpartum hospital readmissions and decreased utilization of emergency departments (ED) for healthcare. 3. Experience higher adherence to American College of Obstetricians and Gynecologists (ACOG) and American Academy of Pediatrics (AAP) guidelines for preventive care, including recently updated ongoing postpartum care, serial well-child visits and vaccinations compared to those assigned to usual care. This group will be compared to those assigned to usual care,
Trial Details
NCT Number NCT06682520
Lead Sponsor Wake Forest University Health Sciences
Collaborators: The Duke Endowment
Conditions
(from sponsor)		 Health Care Utilization
Related terms Patient Acceptance of Health Care
Enrollment 1,300 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov