Actively Recruiting

Age: 18Years - 60Years
All Genders
Healthy Volunteers
ID05243043

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

Led by Stephanie Stewart · Updated on 2025-08-12

80

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to develop, validate, and pilot test an interactive Maternal Resuscitation Navigation Application (MARINA) designed to provide mothers with information and guidance about what to expect during the initial resuscitation of a premature infant in the delivery room. The application includes videos simulating the delivery environment, explanations of each team member's role, and specific resuscitation activities. Content is developed with input from mothers who have experienced premature infant resuscitation to ensure it addresses key concerns and is informed by prior research. The MARINA app allows mothers to choose their preferred level of interactivity, including viewing close-up procedures like positive pressure oxygen delivery and intubation or a broader room view with narration. The app tracks which sections are accessed and the time spent, supporting evaluation of usability and engagement. Development involves iterative testing and review by parents and clinicians for functionality and content validity. Initially, the study is proceeding with a control group only; the intervention phase will begin once the completed app is approved. Participants include mothers admitted for probable premature delivery between 24 and 32 weeks gestation. Control group mothers who experienced premature infant resuscitation without the app complete demographic and trauma-related surveys. Intervention group mothers will later use the app prior to delivery and complete follow-up surveys and interviews assessing usability, distress levels, and feedback. Outcome measures include the Impact of Event Scale-Revised and the Perinatal PTSD Questionnaire-II, tracked from 24 hours to 65 days after the infant's resuscitation.

CONDITIONS

Brief Title

Interactive Resuscitation Application for Mothers About to Experience Premature Infant Resuscitation

Who Can Participate

Age: 18Years - 60Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • English-speaking mothers aged 18 to 60 years
  • Delivered a premature infant between 24 and 32 weeks gestation at the study hospital
  • Infant born during the most recent gestation
Not Eligible

You will not qualify if you...

  • Infant death prior to enrollment
  • Mothers who required general anesthesia during delivery
  • Mothers under active investigation by the Department of Human Services
  • Prisoners
  • Twin gestation pregnancies

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Participants are identified through review of neonatal intensive care unit census and contacted via email and phone for consent and enrollment.

Monitoring

Duration - Up to 65 days post-resuscitation

Participants complete demographic and research surveys after premature infant resuscitation without exposure to the MARINA application.

Surveys are completed via email or text message approximately 31 days or more after delivery.

Monitoring

Duration - From viewing the app through 65 days post-resuscitation

Participants in the intervention group view the MARINA application prior to delivery and complete post-delivery surveys and optional interviews regarding usability.

1 in-person session viewing the app for at least 30 minutes and post-delivery surveys via email or text; optional recorded interview conducted remotely.

Trial Site Locations

Total: 1 location

1

University of Iowa Stead Family Children's Hospital

Iowa City, Iowa, United States, 52242

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Research Team

S

Stephanie Stewart, PhD

T

Timothy Elgin, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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