Can a smartphone app save more newborns? large study tests real-time feedback for resuscitation
NCT ID NCT05963516
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study tested whether a mobile health app called LIVEBORN can help nurse midwives improve how they support newborns who have trouble breathing right after birth. Over 14,000 newborns and their nurses took part. The app gave either real-time guidance or a summary after the event to see which worked better. The goal was to learn how to make newborn resuscitation safer and more effective.
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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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14,680 people
The number who actually took part.
- Started
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Aug 2023
- Finished
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Jun 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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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- 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.
Newborns admitted to a participating health facility who meet the following criteria: Inclusion criteria: * All in-born neonates, either liveborn or intrapartum (i.e., fresh) stillborn, regardless of multiple gestation or maternal complication. Exclusion criteria: * Less than 28 weeks completed gestation (or if gestational age is unknown, birth weight \<1,000 grams), * outborn, * known congenital anomaly, * antepartum (i.e., macerated) stillbirth. Nurse midwives employed at a participating health facility who meet the following criteria: Inclusion criteria: * All midwives and nurses functioning in the role of a midwife who care for newborns at the time of birth during the course of their regular employment. Exclusion criteria: * Unwillingness to consent
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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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Binza
Kinshasa, Democratic Republic of the Congo
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Bondo
Kinshasa, Democratic Republic of the Congo
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Kingasani
Kinshasa, Democratic Republic of the Congo
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Saint Gabriel
Kinshasa, Democratic Republic of the Congo
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Other studies related to the condition(s) this trial covers.