Reducing Adverse Delivery Outcomes Through Teleneonatology: A Feasibility Study
NCT ID: NCT04258722
Last Updated: 2023-12-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
51 participants
INTERVENTIONAL
2020-11-30
2023-01-30
Brief Summary
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Detailed Description
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In this investigation and within a simulated environment, pediatric interns and residents will resuscitate a simulated 25 week infant at delivery assisted by a simulated nurse and respiratory therapist. Participants will be randomized to resuscitation performed either with or without telemedicine facilitated by a neonatologist. The primary outcome will be time to effective ventilation with other secondary outcomes including metrics derived from the American Academy of Pediatrics Neonatal Resuscitation Program.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
OTHER
SINGLE
Study Groups
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Trainee + Teleneonatologist
Trainee, teleneonatologist, nurse, and respiratory therapist will perform resuscitation
Resuscitation Personnel
Type of resuscitation team
Trainee
Trainee, nurse, and respiratory therapist will perform resuscitation.
Resuscitation Personnel
Type of resuscitation team
Interventions
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Resuscitation Personnel
Type of resuscitation team
Eligibility Criteria
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Inclusion Criteria
* Inclusion criteria for experienced providers include at least 3 years of pediatric and/or neonatal training, having previously performed \>10 endotracheal intubations, and may include neonatologists, pediatric fellows, and neonatal nurse practitioners. Inclusion criteria for trainees: previous exposure to NRP, an interval of \> 3 months elapsing between previous NRP applications, and may include pediatric residents, family medicine residents, nurses, respiratory therapists, neonatal fellows, and neonatal attendings.
Exclusion Criteria:
* Does not meet inclusion criteria
18 Years
75 Years
ALL
Yes
Sponsors
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University of Alabama at Birmingham
OTHER
Responsible Party
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Samuel Gentle
Assistant Professor
Principal Investigators
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Samuel Gentle, MD
Role: PRINCIPAL_INVESTIGATOR
University of Alabama at Birmingham
Locations
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Children's of Alabama at Birmingham
Birmingham, Alabama, United States
Countries
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Other Identifiers
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IRB-300004483
Identifier Type: -
Identifier Source: org_study_id