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.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 60 Years |
| Sex | All |
| Enrollment | 80 (estimated) |
| Sponsor | University of Iowa Academic / other |
| Locations | 1 site (Iowa City, Iowa) |
| Status | Recruiting |
| Started | August 31, 2022 |
| Main results expected | December 2027 |
| Study ends | December 2027 |
| Registry record updated | August 12, 2025 |
| Trial ID | NCT05243043 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
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Super-Early Neuroprognostication in eCPR Patients
This observational study tests whether rapid brain-status measurements taken early after ECMO initiation can help predict neurological outcomes in adults considered for eCPR.
-
Network for evaluating delivery room resuscitation practices in newborns
This study is testing how different ways of helping newborns breathe at birth can improve their chances of survival and overall care in hospitals across the U.S.
-
Examining emergency department management for out-of-hospital cardiac arrest patients
This study looks at how different treatments in the emergency department can help improve survival and brain function for adults who have had a cardiac arrest outside the hospital.
-
Pre-hospital wearable cooling after out-of-hospital cardiac arrest
This pilot test tries a battery-free CarbonCool® cooling vest applied by paramedics to adults who regain a pulse after out-of-hospital cardiac arrest but remain unconscious to see if early cooling is feasible and safe.
-
Measuring how well people estimate lengths and depths in CPR scenarios
This study tests how accurately regular people and healthcare providers can estimate lengths and depths in CPR situations to see if they need better training.
-
Improving survival rates for out-of-hospital cardiac arrest using advanced CPR techniques
This study is testing new CPR techniques and devices to see if they can help adults who have a cardiac arrest outside of the hospital survive and maintain normal brain function.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.