Healing, Equity, Advocacy and Respect for Mamas
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.
Conditions:
🦠 Postpartum Complication
🗓️ Study Start (Actual) 28 May 2024
🗓️ Primary Completion (Estimated) 30 November 2028
✅ Study Completion (Estimated) 30 November 2028
👥 Enrollment (Estimated) 2894
🔬 Study Type INTERVENTIONAL
📊 Phase NA
Locations:
📍 Charleston, South Carolina, United States

📋 Eligibility Criteria

Description

  • Inclusion Criteria for Postpartum Women
  • * Admitted to the Roper St. Francis HealthCare Postpartum Unit following delivery
  • * Postpartum woman within approximately 2 weeks of delivering a baby of gestational age ≥ 26 weeks.
  • * Aged 18-49 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.
  • * 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.
Ages Eligible for Study: 18 Years to 49 Years (ADULT)
Sexes Eligible for Study: FEMALE
Accepts Healthy Volunteers: No

🗓️ Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

  • First Submitted 27 January 2024
  • First Submitted that Met QC Criteria 15 February 2024
  • First Posted 22 February 2024

Study Record Updates

  • Last Update Submitted that Met QC Criteria 21 July 2024
  • Last Update Posted 23 July 2024
  • Last Verified July 2024