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Postpartum Video Education in High Risk Populations
This is a prospective, single-center, randomized control study to determine if video education at the time of postpartum discharge improves patient knowledge on the warning signs for the top three causes of severe maternal morbidity (infection, hemorrhage, and blood pressure disorders) in the first seven days following delivery for self-identified, Black, Latinx, other with two or more self-identified races, Medicaid, and/or uninsured postpartum individuals. Participants will be randomized to written discharge education + video education (intervention) vs standard discharge education (control). They will complete a baseline questionnaire and a post-discharge education questionnaire during their postpartum stay to assess for knowledge improvement. The investigators hypothesize that video education will improve patient's knowledge of severe maternal morbidity warning signs.
Conditions:
🦠 Postpartum Hemorrhage 🦠 Postpartum Depression 🦠 Postpartum Sepsis 🦠 Postpartum Preeclampsia 🦠 Patient Empowerment 🦠 Patient Education 🦠 Postpartum Care
🗓️ Study Start (Actual) 9 May 2024
🗓️ Primary Completion (Estimated) December 2024
✅ Study Completion (Estimated) December 2024
👥 Enrollment (Estimated) 150
🔬 Study Type INTERVENTIONAL
📊 Phase NA
Locations:
📍 New York, New York, United States

📋 Eligibility Criteria

Description

    Inclusion Criteria:

    • * Age \>18 years
    • * Speaks English or Spanish
    • * Informed and written consent
    • * Delivered at WCM
    • * Received prenatal, and will receive postpartum, care through a WCM-affiliated obstetric and/or midwifery practice
    • * Self-identified as Black, Latinx, other and/or Medicaid or Uninsured

    Exclusion Criteria:

    • * Patients who do not plan to receive postpartum care within the WCM system
    • * Patients who experience an intrauterine fetal demise
    • * Patients who speak a primary language other than English or Spanish
Ages Eligible for Study: 18 Years to N/A (ADULT, OLDER_ADULT)
Sexes Eligible for Study: FEMALE
Accepts Healthy Volunteers: Yes

🗓️ 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 7 March 2024
  • First Submitted that Met QC Criteria 7 March 2024
  • First Posted 15 March 2024

Study Record Updates

  • Last Update Submitted that Met QC Criteria 22 May 2024
  • Last Update Posted 24 May 2024
  • Last Verified May 2024
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