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NCT06572033 · ClinicalTrials.gov registry record
Transference of Established Simulated Skills (TEST) Trial
A clinical trial of Neonatal Respiratory Distress, sponsored by University of Texas Southwestern Medical Center.
- Recruiting
- Registry status
- 120
- Enrollment target
- 1
- Study location
NCT06572033: Recruiting study of Neonatal Respiratory Distress, sponsored by University of Texas Southwestern Medical Center.
NCT06572033 is a study of Neonatal Respiratory Distress that is actively recruiting participants, run by University of Texas Southwestern Medical Center. The registered enrollment target is 120 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06572033, a study of Neonatal Respiratory Distress, is actively recruiting participants, sponsored by University of Texas Southwestern Medical Center.
- RECRUITING
- Registry status
- 120 participants
- Enrollment target
- 1
- Study location
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.
Primary Outcome
Correlation between the percentage of mask leak observed during positive pressure ventilation (PPV) on a mannequin in the simulation laboratory and the percentage of mask leak observed during PPV on a newborn infant in the delivery room.
Conditions Studied
Interventions
- BEHAVIORAL Simulation
Study Locations (1)
Texas
- Parkland Memorial Hospital - Dallas
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2024-08-12 |
| Est. Completion | 2025-12-29 |
What NCT06572033 shows while recruiting
NCT06572033 is an observational study that tracks outcomes without assigning an intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap.
The record links to 1 condition, with Neonatal Respiratory Distress appearing as the primary indexed condition, and to 1 intervention - of which Simulation is the first listed.
NCT06572033 reports a single indexed study location in Texas.
Frequently Asked Questions
What is clinical trial NCT06572033 about?
NCT06572033 is a clinical study titled "Transference of Established Simulated Skills (TEST) Trial". 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 newbo...
What is the current status of trial NCT06572033?
This trial is currently recruiting. The enrollment target is 120 participants. The study started on 2024-08-12. Estimated completion is 2025-12-29.
What conditions does trial NCT06572033 study?
This clinical trial studies the following conditions: Neonatal Respiratory Distress.
What interventions are being tested in trial NCT06572033?
The interventions under investigation include: Simulation (BEHAVIORAL).
Who is sponsoring clinical trial NCT06572033?
This trial is sponsored by University of Texas Southwestern Medical Center, which has 837 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06572033 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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