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Recruiting
NCT06273436
Healing, Equity, Advocacy and Respect for Mamas
Conditions: Postpartum Complication
Sex: Female
Ages: 16 Years – 49 Years
Healthy volunteers: No
Phase: NA
Enrollment: 2894
Sponsor: Medical University of South Carolina
Location: Medical University of South Carolina Charleston South Carolina
Summary
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.
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.
Source: ClinicalTrials.gov (NCT06273436). StuddyBuddy aggregates publicly available trial information.