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Healing, Equity, Advocacy and Respect for Mamas
RecruitingMentions payment for participants
Comparing Standard of Care Versus a Technology-Based Approach To Reduce Postpartum Emergency Department Visits
Who can join
Ages 16 to 49 · Women
Full eligibility criteria
Inclusion Criteria for Postpartum Women * Postpartum woman within approximately 2 weeks of delivering a baby of gestational age ≥ 26 weeks in South Carolina. * Aged 16-49 years old. * Insured by Medicaid. Exclusion Criteria for Postpartum Women * Plans to relocate outside of SC anytime during the postpartum year. * Plans to discontinue Medicaid health insurance during the postpartum year. * Speaks a language other than English or Spanish. * Incarcerated/pending incarceration during peripartum period. * Currently institutionalized. * Enrolled in current MUSC study funded by PCORI (#Pro00123833) * Does not have and/or does not wish to use their personal cell phone for the study. Inclusion Criteria for Obstetric Providers and Hospital Administrators \- OB provider working at a delivery hospital in SC and directly involved in the care of postpartum women; or hospital administrator working in a delivery hospital in SC and job responsibilities relate to the postpartum unit. Exclusion Criteria for Obstetric Providers and Hospital Administrators * Less than 1 month of HEAR 4 Mamas experience if involved in the hospital where participants are recruited from. * Unable or unwilling to commit to completing surveys or an interview. * Speaking a language other than English.
About the study
The goal of the proposed research is to test the comparative effectiveness of AIM safety bundles for post-partum women delivered in-person vs. via text/phone to improve early detection of and timely care for complications during the first six weeks postpartum for women experiencing significant health disparities.
What is being tested
- H.E.A.R. for Mamas (other)
Sponsor: Medical University of South Carolina · Participants: 2,894 · Started: May 28, 2024
Contact the study team
- Constance Guille, MD · Phone: 843-792-6489
- Edie Douglas · Phone: 8439985635
Official record on ClinicalTrials.gov — NCT06273436
Locations in the U.S.
| South Carolina | Medical University of South Carolina, Charleston |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.