Clinical trial Recruiting at 1 site Observational Ages 18 to 60

An app to help mothers understand premature infant resuscitation

Official title: Impact of an Interactive Maternal Resuscitation Navigation Application (MARINA) on Mothers' Experience During and After Premature Infant Resuscitation in the Delivery Room

Run by University of Iowa · NCT05243043 · Data updated 2026-11-12

This study is testing a new app that helps mothers understand what happens during resuscitation for premature infants before delivery.

More Cardiopulmonary Resuscitation trials

Quick facts

Study typeObservational
Ages18 Years to 60 Years
SexAll
Enrollment80 (estimated)
SponsorUniversity of Iowa
Academic / other
Locations1 site (Iowa City, Iowa)
StatusRecruiting
StartedAugust 31, 2022
Main results expectedDecember 2027
Study endsDecember 2027
Registry record updatedAugust 12, 2025
Trial IDNCT05243043 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are English-speaking mothers aged 18 or older who have delivered a premature infant at the University of Iowa Hospitals and Clinics between 24 and 32 weeks of gestation.

Probably not a fit

Patients who may not benefit from this study include those whose infants did not survive, mothers who required general anesthesia during delivery, and those involved in active investigations by the Department of Human Services.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to design and pilot test an interactive application called MARINA, which provides mothers with information and guidance about premature infant resuscitation before delivery. The app will feature high-fidelity simulation videos that depict the delivery environment and explain the roles of medical team members during resuscitation. Input from mothers who have experienced premature infant resuscitation will be used to ensure the app addresses their key concerns. The pilot testing will evaluate the app's functionality, usability, and feasibility for future clinical use.

Why it matters

Potential benefit: If successful, this app could significantly reduce maternal anxiety and improve the overall experience for mothers during the stressful time of premature infant resuscitation.

How similar studies have gone: While similar applications have been developed for patient education, this specific approach focusing on premature infant resuscitation is novel and has not been extensively tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Control group: English-speaking mothers, age 18 or older, delivered a premature infant at UIHC between 24- and 32-weeks and their infant born during this most recent gestation.

Exclusion Criteria:

* control group: Infant death, mothers who required general anesthesia at the time of delivery, active investigation by Department of Human Services, prisoners, twin gestation

Where it's running

  • University of Iowa Stead Family Children's Hospital
    Iowa City, Iowa, United States
    Recruiting

Study contacts

  • Principal investigator: Stephanie Stewart, PhD — University of Iowa Stead Family Children's Hospital
  • Study coordinator: Stephanie Stewart, PhD
  • Email: stephanie-stewart@uiowa.edu
  • Phone: 3193537999

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.