SUSPENDED

Postpartum Video Education in High Risk Populations

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

You Matter: Using Video Education to Improve Patient Knowledge of Severe Maternal Morbidity Warning Signs in High Risk Populations

Quick Facts

Study Start:2024-05-09
Study Completion:2027-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:SUSPENDED

Study ID

NCT06310720

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age \>18 years
  2. * Speaks English or Spanish
  3. * Informed and written consent
  4. * Delivered at WCM
  5. * Received prenatal, and will receive postpartum, care through a WCM-affiliated obstetric and/or midwifery practice
  6. * Self-identified as Black, Latinx, other and/or Medicaid or Uninsured
  1. * Patients who do not plan to receive postpartum care within the WCM system
  2. * Patients who experience an intrauterine fetal demise
  3. * Patients who speak a primary language other than English or Spanish

Contacts and Locations

Principal Investigator

Heather Lipkind, MD, MSce
PRINCIPAL_INVESTIGATOR
Weill Medical College of Cornell University

Study Locations (Sites)

Alexandra Cohen Hospital for Women and Newborns
New York, New York, 10065
United States

Collaborators and Investigators

Sponsor: Weill Medical College of Cornell University

  • Heather Lipkind, MD, MSce, PRINCIPAL_INVESTIGATOR, Weill Medical College of Cornell University

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

Study Start Date2024-05-09
Study Completion Date2027-12

Study Record Updates

Study Start Date2024-05-09
Study Completion Date2027-12

Terms related to this study

Additional Relevant MeSH Terms

  • Postpartum Hemorrhage
  • Postpartum Depression
  • Postpartum Sepsis
  • Postpartum Preeclampsia
  • Patient Empowerment
  • Patient Education
  • Postpartum Care