Healing, Equity, Advocacy and Respect for Mamas
Recruiting
N/A
Interventional Study
Postpartum Complication
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 16 – 49
- Sex
- Female
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 2,894 (estimated)
- Sponsor
- Medical University of South Carolina · Other
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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.
Trial Locations
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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…
Contacts