NCT06273436 Healing, Equity, Advocacy and Respect for Mamas
| NCT ID | NCT06273436 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Medical University of South Carolina |
| Condition | Postpartum Complication |
| Study Type | INTERVENTIONAL |
| Enrollment | 2,894 participants |
| Start Date | 2024-05-28 |
| Primary Completion | 2028-11-30 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 2,894 participants in total. It began in 2024-05-28 with a primary completion date of 2028-11-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief 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.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06273436 clinical trial?
This trial is open to female participants only, aged 16 Years or older, up to 49 Years, studying Postpartum Complication. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06273436 currently recruiting?
Yes, NCT06273436 is actively recruiting participants. Contact the research team at guille@musc.edu for enrollment information.
Where is the NCT06273436 trial being conducted?
This trial is being conducted at Charleston, United States.
Who is sponsoring the NCT06273436 clinical trial?
NCT06273436 is sponsored by Medical University of South Carolina. The trial plans to enroll 2,894 participants.