Transference of Established Simulated Skills (TEST) Trial

Phase

N/A

Condition

Lung Injury

Respiratory Failure

Treatment

Simulation

Clinical Study ID

NCT06572033

STU 2023-1099

All Genders
Accepts Healthy Volunteers

Study Summary

This study aims to determine if skills learned in the simulation lab, specifically in managing mask leak during positive pressure ventilation (PPV), translate effectively to the delivery room. By comparing the performance of healthcare providers on mannequins in the lab to their performance on newborns in the delivery room, the study seeks to establish a Ventilation Performance Score (VPS) based on data from a respiratory function monitor. The primary hypothesis is that a provider's ability to minimize mask leak on a mannequin correlates with their ability to do so with a newborn. The prospective observational TEST Trial will use the Monivent Neo100 to collect and analyze PPV data, comparing key parameters like mask leak and VQS between the two settings to assess correlations. Secondary analysis will explore individual aspects of PPV, such as PIP, PEEP, and eVT.

Eligibility Criteria

Inclusion

Inclusion and Exclusion Criteria for Respiratory Therapists (RTs)

Inclusion Criteria:

Respiratory Therapists who are employed in the Neonatal Intensive Care Unit (NICU)at Parkland Hospital.
RTs who actively participate in neonatal deliveries.

Exclusion

Exclusion Criteria:

Respiratory Therapists classified as "float" RTs, meaning those who do not have apermanent assignment in the NICU.
RTs who intend to leave the institution within the upcoming year.

Inclusion and Exclusion Criteria for Newborn Infants

Inclusion Criteria:

Newborn infants who require positive pressure ventilation (PPV) immediately afterbirth in the delivery room.
Infants of various gestational ages and birth weights, representing a broad spectrumof neonatal resuscitation scenarios.

Exclusion Criteria:

Newborns who do not require PPV after birth.
Infants for whom the use of the respiratory function monitor (RFM) is not feasibledue to medical or technical reasons.

Study Design

Simulation

August 12, 2024

May 29, 2025

Study Description

Objectives: The aim of this study is to establish evidence that supports the transfer of skills learned in the simulation lab to the delivery room. The objective of this study is to compare the performance of positive pressure ventilation (PPV) in the simulation lab to the performance of the same individual in the delivery room. Our goal is to establish a comparison between parameters measured on the simulator and those obtained from real newborn infants, specifically looking at mask leak. Our approach hopes to develop a ventilation performance score (VPS) in the process that will be based on objective data collected using a respiratory function monitor (RFM). The primary hypothesis is that the quality of a qualified provider's ability to circumvent mask leak on a mannequin correlates with the ability of the same provider to circumvent mask leak observed on a newborn infant.

Design and outcomes: TEST Trial is a prospective observational study to assess differences in the participants ability to avoid mask leak while performing PPV and in the process allow the investigators to develop a ventilatory performance score in the simulation lab and the delivery room. We will use the RFM Monivent Neo100 to gather PPV data in both the simulation lab from the mannequins and newborns in the delivery room. The study will compare mask leak as well as VPS in the simulation room to mask leak and VPS in the delivery room to assess for correlations. In addition, the investigators will conduct secondary analysis on each individual domain of positive pressure ventilation, such as PIP, PEEP, eVT, etc.

Connect with a study center

Parkland Memorial Hospital
Dallas, Texas 75235
United States
Active - Recruiting

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