Reducing Adverse Delivery Outcomes Through Teleneonatology: A Feasibility Study

The University of Alabama at Birmingham

Status: Completed

Conditions: Newborn Morbidity

Treatments: Other: Resuscitation Personnel

Study type: Interventional

Funder types: Other

Identifiers

NCT04258722

IRB-300004483

Details and patient eligibility

About

Teleneonatology, the use of audio-video communication to facilitate neonatal-perinatal care, may bridge the resuscitation quality gap by connecting centers with lower level care to experienced care providers. Using randomized trial design, this investigation will compare teleneonatal resuscitation facilitated by a neonatologist to standard resuscitation within a simulated environment.

Full description

Multiple studies have evaluated telemedicine using simulation, but the level of evidence for the use of telemedicine to improve neonatal resuscitation is low.

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.

Enrollment: 51 patients

Sex: All

Ages: 18 to 75 years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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51 participants in 2 patient groups

Trainee + Teleneonatologist

Experimental group

Description:

Trainee, teleneonatologist, nurse, and respiratory therapist will perform resuscitation

Treatment:

Other: Resuscitation Personnel

Trainee

Active Comparator group

Description:

Trainee, nurse, and respiratory therapist will perform resuscitation.

Treatment:

Other: Resuscitation Personnel