A 12-minute video could save new mothers' lives – can it teach them to spot danger?
NCT ID NCT06310720
First seen Aug 21, 2026 · Last updated Aug 21, 2026
Summary
This trial tests whether a 12-minute educational video, shown at hospital discharge, improves new mothers' knowledge of warning signs for severe postpartum complications like hemorrhage, infection, and high blood pressure. Participants – who are Black, Latinx, multiracial, Medicaid, or uninsured – are randomly assigned to receive the video plus standard written instructions, or standard care alone. They complete questionnaires to measure knowledge before and after the education. The goal is to see if video education can empower mothers to recognize danger signs in the first week after delivery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A 12-minute educational video covering postpartum warning signs for hemorrhage, infection, hypertension, and depression.
- What this could lead to
- If effective, this approach could become a standard tool to help new mothers recognize dangerous symptoms early, potentially reducing severe postpartum complications.
- What could go wrong
- The trial is small (50 participants) and measures knowledge improvement, not actual health outcomes. Video education may not translate into real-world recognition or action, and results may not apply to broader populations.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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50 people
The number who actually took part.
- Started
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May 2024
- Finished
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Sep 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Alexandra Cohen Hospital for Women and Newborns
New York, New York, 10065, United States
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