Healing, Equity, Advocacy and Respect for Mamas
ConditionPostpartum Complication
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age16-49
SponsorMedical University of South Carolina
About this trial
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
Qualifiers
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.
Disqualifiers
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.
Trial design
Treatments tested in this trial
- H.E.A.R. for Mamas
Treatment groups
2,894 Participants
are divided into 2 treatment groupsSponsors and collaborators
Medical University of South Carolina
Lead sponsor
Patient-Centered Outcomes Research Institute
Collaborator
Source ClinicalTrials.gov