Visual Perception Exploration Using Eye-tracking Technology in a Cannot Intubate/Cannot Oxygenate Simulation
1 other identifier
observational
14
0 countries
N/A
Brief Summary
Using eye-tracking technology, the aim of this observational study is to compare the visual interests between attending physicians and residents watching a Cannot Intubate/Cannot Oxygenate (CICO) scripted and simulated scenario
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Jul 2016
Shorter than P25 for all trials
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 Start
First participant enrolled
July 1, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2017
CompletedFirst Submitted
Initial submission to the registry
February 7, 2017
CompletedFirst Posted
Study publicly available on registry
February 15, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2017
CompletedMay 2, 2017
May 1, 2017
7 months
February 7, 2017
May 1, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Difference between Time to First Fixation and Total View Duration of areas of interests.
The screen was equipped with TobiiEyeX®, an eye-tracking system that automatically aggregates gaze data. The display was divided in seven Areas of Interest (AOI). Data were collected using the Tobii Studio® program to obtain the total view duration (TVD) of the various AOIs.
The primary endpoint is collected during 15 minutes, throughout the viewing of the video by the participant
Study Arms (2)
Residents
Anesthesia residents from University of Montreal Anesthesia Department who were watching the video
Attending Physicians
Attending physicians from University of Montreal Anesthesia Department who were watching the video
Interventions
A 13-minute video based on a suggested CICO algorithm from the Difficult Airway Society that was produced at the University of Montreal Simulation Centre using high-fidelity settings.
Eligibility Criteria
Residents and attending physicians from University of Montreal Anesthesia Department
You may qualify if:
- Residents and attending physicians from University of Montreal Anesthesia Department
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Issam Tanoubi, Dr
Université de Montreal
- PRINCIPAL INVESTIGATOR
Komi Sodoke, Msc
Université de Montreal
- PRINCIPAL INVESTIGATOR
Mathieu Tourangeau, Dr
Université de Montreal
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Université de Montreal
Study Record Dates
First Submitted
February 7, 2017
First Posted
February 15, 2017
Study Start
July 1, 2016
Primary Completion
February 1, 2017
Study Completion
April 1, 2017
Last Updated
May 2, 2017
Record last verified: 2017-05
Data Sharing
- IPD Sharing
- Will not share