Actively Recruiting
Comparing Standard of Care Versus a Technology-Based Approach To Reduce Postpartum Emergency Department Visits
Led by Medical University of South Carolina · Updated on 2026-02-17
2894
Participants Needed
1
Research Sites
69 weeks
Total Duration
On this page
Sponsors
M
Medical University of South Carolina
Lead Sponsor
P
Patient-Centered Outcomes Research Institute
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying postpartum women to compare two methods of delivering safety and health monitoring: traditional in-person care versus a technology-based program using text messages and phone calls. The aim is to improve early detection and timely care for complications during the first six weeks after giving birth, especially for women facing health disparities. This study is supported by the Medical University of South Carolina and focuses on reducing emergency department visits postpartum. Participants will be assigned randomly to either usual in-person postpartum care or usual care plus the H.E.A.R. for Mamas program. The H.E.A.R. program uses simple text or phone screenings to regularly check for signs of postpartum complications, chronic conditions, and social factors affecting health. If concerns arise, a nurse advocate will follow up by phone to discuss care options and referrals. The study includes surveys completed via cell phone or email at enrollment and three additional times throughout the year. Women will be followed for one year after delivery, completing surveys at enrollment, 3, 6, and 12 months postpartum. Researchers will monitor emergency department visits within six weeks after delivery as the main outcome. Participant-reported outcomes will also be collected through surveys. The study tracks health and social needs using phone and text technology, with participants receiving payment for completing surveys.
CONDITIONS
Brief Title
Healing, Equity, Advocacy and Respect for Mamas
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Postpartum woman within approximately 2 weeks of delivering a baby of gestational age 6 weeks in South Carolina
- Aged 16 to 49 years old
- Insured by Medicaid
- Obstetric providers or hospital administrators working at delivery hospitals in South Carolina involved in postpartum care (for provider/administrator participants)
You will not qualify if you...
- Plans to relocate outside of South Carolina during the postpartum year
- Plans to discontinue Medicaid insurance during the postpartum year
- Speaks a language other than English or Spanish
- Is incarcerated or pending incarceration during the peripartum period
- Currently institutionalized
- Enrolled in current MUSC study funded by PCORI (#Pro00123833)
- Does not have or does not wish to use a personal cell phone for the study
- Obstetric providers or hospital administrators with less than one month of H.E.A.R. for Mamas experience at the recruiting hospital
- Unable or unwilling to complete surveys or interviews
- Speaks a language other than English (for providers/administrators)
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 screening and enrollment visit (can be completed via cell-phone or email)
Duration - Up to 6 weeks postpartum
Participants receive usual in-person postpartum care with or without the addition of a text message-based program that monitors for signs and symptoms of postpartum complications and provides feedback and recommendations.
Ongoing text message screenings with nurse advocate follow-up calls as needed during this period
Duration - Up to 12 months postpartum
Participants complete surveys at 3, 6, and 12 months postpartum to report on their health status and outcomes after delivery.
3 surveys completed via cell-phone or email at 3, 6, and 12 months postpartum
Trial Site Locations
Total: 1 location
1
Medical University of South Carolina
Charleston, South Carolina, United States, 29425
Actively Recruiting
Research Team
C
Constance Guille, MD
E
Ellen H Gomez, MA
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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