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Terminated
NCT06310720
Postpartum Video Education in High Risk Populations
Conditions: Postpartum Hemorrhage, Postpartum Depression, Postpartum Sepsis, Postpartum Preeclampsia, Patient Empowerment, Patient Education, Postpartum Care
Sex: Female
Ages: 18 Years – N/A
Healthy volunteers: Yes
Phase: NA
Enrollment: 50
Sponsor: Weill Medical College of Cornell University
Location: Alexandra Cohen Hospital for Women and Newborns New York New York
Summary
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.
Eligibility Criteria
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
Source: ClinicalTrials.gov (NCT06310720). StuddyBuddy aggregates publicly available trial information.
