Actively Recruiting
Evaluation of a Health System Integrated Model for Postpartum Education and Support in Rural Populations - NEST-Rural
Led by Wake Forest University Health Sciences · Updated on 2025-10-28
1300
Participants Needed
1
Research Sites
130 weeks
Total Duration
On this page
Sponsors
W
Wake Forest University Health Sciences
Lead Sponsor
T
The Duke Endowment
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating the Nurse Education and Support Team (NEST) Program for postpartum women living in five rural counties in North Carolina. This randomized control trial compares the NEST-Rural care model to usual postpartum care to see if mothers and infants receive more coordinated care, experience fewer hospital readmissions and emergency visits, and have better adherence to recommended postpartum and infant care guidelines. The study enrolls about 1,300 mother-infant pairs who deliver at the Atrium Health Wake Forest Baptist Birth Center. Participants are randomly assigned to either the NEST-Rural group or usual care. The NEST-Rural program includes 3-5 nurse visits, remote blood pressure monitoring using a device connected to a smartphone app, breastfeeding support, infant weight checks, social work visits if needed, and coordination with healthcare providers. Usual care includes standard postpartum visits and a follow-up call. During the study, participants will have nurse or social worker visits at home or via telehealth, remote monitoring of maternal blood pressure, and follow-up phone calls. Researchers will track hospital readmissions, emergency care visits, attendance at postpartum and infant well-child visits, breastfeeding rates, and immunizations. Safety and healthcare utilization will be monitored over periods ranging from 21 days to two years postpartum, with data collected through medical records and nurse reports.
CONDITIONS
Brief Title
Evaluation of a Health System Integrated Model for Postpartum Education and Support in Rural Populations
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women who deliver an infant(s) at The Birth Center at Atrium Health Wake Forest Baptist and currently live in Davidson, Davie, Stokes, Wilkes, or Yadkin County, North Carolina
- Women who delivered an infant(s) at home, were transported to Atrium Health Wake Forest Baptist, and currently live in Davidson, Davie, Stokes, Wilkes, or Yadkin County, North Carolina
- Women aged 18 years or older
You will not qualify if you...
- Women who delivered an infant(s) but did not receive postpartum care at The Birth Center at Atrium Health Wake Forest Baptist
- Women who currently live outside Davidson, Davie, Stokes, Wilkes, or Yadkin County, North Carolina
- Women under 18 years of age
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 6 weeks postpartum
Participants randomized to the NEST-Rural Program will receive 3 to 5 nurse encounters and up to 3 social work encounters with mothers and their infants, postpartum remote blood pressure monitoring, breastfeeding support, infant weight checks, and linkage to needed social, behavioral, and health-related resources. Services start in the postpartum hospital unit with a coordinator introduction and include home or telehealth nurse visits and follow-ups.
3 to 5 nurse visits and up to 3 social work visits (home or telehealth), plus a coordinator phone call at 6 weeks postpartum
Duration - Up to 6 weeks postpartum
Participants randomized to usual care receive standard postpartum care from their obstetrics provider with a follow-up phone call from a coordinator at about 6 weeks postpartum, along with information about community services and resources.
1 follow-up phone call at about 6 weeks postpartum
Trial Site Locations
Total: 1 location
1
Atrium Health Wake Forest Baptist
Winston-Salem, North Carolina, United States, 27157
Actively Recruiting
Research Team
E
Elizabeth T. Jensen, MPH PhD
D
David M. Stamilio, MD, MSCE
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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