- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07518849
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
Status
Not yet recruiting
Intervention / Treatment
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
- Name: Jason Hayes, MD
- Phone Number: 416-813-7445
- Email: jason.hayes@sickkids.ca
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
|
|
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.
Sponsor
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
Keywords
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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