NCT07518849

Brief Summary

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.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
4mo left

Started Jun 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress34%
Jun 2026Dec 2026

First Submitted

Initial submission to the registry

March 26, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

April 9, 2026

Completed
2 months until next milestone

Study Start

First participant enrolled

June 1, 2026

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

April 9, 2026

Status Verified

March 1, 2026

Enrollment Period

6 months

First QC Date

March 26, 2026

Last Update Submit

April 2, 2026

Conditions

Keywords

AnesthesiaErgonimcsSimulation

Outcome Measures

Primary Outcomes (1)

  • Crisis performance

    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 Outcomes (5)

  • Time metrics

    Measured during the crisis scenario, average time is 5 minutes

  • Case management score

    Measured during the crisis scenario, average time is 5 minutes

  • Ergonomic/motor metrics

    Measured during the crisis scenario, average time is 5 minutes

  • Workload measurement metrics

    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

    Measured during the crisis scenario, average time is 5 minutes

Study Arms (2)

Preferred/optimal position group

EXPERIMENTAL

Anesthesia machine is placed on the preferred side and optimal position for the anesthesiologist

Behavioral: Simualted laryngospasm crisis

Non-preferred/awkward position group

ACTIVE COMPARATOR

Anesthesia machine is placed on the non-preferred side and awkward position for the anesthesiologist

Behavioral: Simualted laryngospasm crisis

Interventions

An acute laryngospasm scenario will be simulated in a pediatric manikin

Non-preferred/awkward position groupPreferred/optimal position group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • Unwillingness to complete the simulated crisis and complete study questionnaires

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Two groups randomized to anesthesia machine in the "preferred/optimal" or "non-preferred/awkward" position while managing a short, simulated anesthesia crisis followed by 1-minute to perform bag-valve-mask ventilation.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Staff Anesthesiologist

Study Record Dates

First Submitted

March 26, 2026

First Posted

April 9, 2026

Study Start

June 1, 2026

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

April 9, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share