Effect of Anesthesia Equipment Position on Anesthesiologists' Performance

April 2, 2026 updated by: Jason Hayes, The Hospital for Sick Children

The Effect of Anesthesia Equipment Position on Anesthesiologists' Crisis Management and Bag-valve-mask Ventilation Using Full Scale Simulation.

The purpose of this study is to determine if the position of the anesthesia machine affects the ability of anesthesiologists to manage a crisis situation and perform critical tasks. Participants will be asked to manage a simulated crisis situation using a manikin in the operating room. The anesthesia machine will be positioned either in an "optimal" or "awkward" manner for the anesthesiologist. The session will be video recorded and then analysed for various outcomes that reflect the anesthesiologist's performance. Participants will also perform a critical task, bag-valve-mask ventilation, on a manikin with the anesthesia machine in the optimal and awkward positions. The effectiveness of ventilation in each position will be compared. The results of this study may have implications for patient safety.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • All Department of Anesthesia residents (PGY4 or 5), fellows and staff are eligible to participate.

Exclusion Criteria:

  • Unwillingness to complete the simulated crisis and complete study questionnaires

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Preferred/optimal position group
Anesthesia machine is placed on the preferred side and optimal position for the anesthesiologist
An acute laryngospasm scenario will be simulated in a pediatric manikin
Active Comparator: Non-preferred/awkward position group
Anesthesia machine is placed on the non-preferred side and awkward position for the anesthesiologist
An acute laryngospasm scenario will be simulated in a pediatric manikin

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Crisis performance
Time Frame: Measured during the crisis scenario, average time is 5 minutes
A composite performance score defined as the mean of standardized MEPA checklist score and standardized time to scenario completion.
Measured during the crisis scenario, average time is 5 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Time metrics
Time Frame: Measured during the crisis scenario, average time is 5 minutes
Time from change in vital signs to intervention
Measured during the crisis scenario, average time is 5 minutes
Case management score
Time Frame: Measured during the crisis scenario, average time is 5 minutes
Performance of predefined key tasks in the treatment of the simulated crisis
Measured during the crisis scenario, average time is 5 minutes
Ergonomic/motor metrics
Time Frame: Measured during the crisis scenario, average time is 5 minutes
  1. Number of times the hand(s) cross the midline and touches the machine or equipment
  2. Number of times the anesthesiologist makes an adjustment to optimize BVM ventilation attempts:
  3. Total number of degrees the anesthesiologist's head turns during the scenario
  4. Total distance the anesthesiologist's hand travels during the scenario
Measured during the crisis scenario, average time is 5 minutes
Workload measurement metrics
Time Frame: Questionnaire is completed after the participation in the crisis scenario is completed. The questionnaire will take an average of 10 minutes to complete.
National Aeronautics and Space Administration Task Load questionnaire
Questionnaire is completed after the participation in the crisis scenario is completed. The questionnaire will take an average of 10 minutes to complete.
Minute ventilation
Time Frame: Measured during the crisis scenario, average time is 5 minutes
Measurement of the minute ventilation during performance of bag-valve-mask ventilation on a manikin with the anesthesia machine in both the preferred and non-preferred positions.
Measured during the crisis scenario, average time is 5 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

June 1, 2026

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2026

Study Registration Dates

First Submitted

March 26, 2026

First Submitted That Met QC Criteria

April 2, 2026

First Posted (Actual)

April 9, 2026

Study Record Updates

Last Update Posted (Actual)

April 9, 2026

Last Update Submitted That Met QC Criteria

April 2, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • 4200

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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