The Effect of Identification Badge on Situation Awareness During High Fidelity Simulation
1 other identifier
interventional
28
1 country
1
Brief Summary
The purpose of this study is to evaluate if the use of identification badge (role and place) during high-fidelity simulation as an impact on situation awareness.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Apr 2014
Shorter than P25 for not_applicable
1 active site
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
First Submitted
Initial submission to the registry
March 25, 2014
CompletedStudy Start
First participant enrolled
April 1, 2014
CompletedFirst Posted
Study publicly available on registry
April 7, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2014
CompletedDecember 2, 2014
December 1, 2014
4 months
March 25, 2014
December 1, 2014
Conditions
Outcome Measures
Primary Outcomes (1)
Situation awareness
Subjects answer a 4 questions survey on situation awareness with 7 answers choices (1-strongly disagree... 7-strongly agree) 1. I know where I was in the beginning of the scenario 2. I know where I was during the scenario 3. I know the role of each participant in the beginning of the scenario 4. I Know the role of each participant during the scenario
2 days
Secondary Outcomes (1)
Subject's engagement in high-fidelity simulation
2 days
Study Arms (2)
Scenario C (control)
NO INTERVENTIONno badge
Scenario B (badge)
ACTIVE COMPARATORUse of Identification badge during scenarios (roles and places)
Interventions
Eligibility Criteria
You may qualify if:
- anesthesiology residents (university of montreal) who participate to simulation course on crisis resources management
You may not qualify if:
- none
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CAAHC
Montreal, Quebec, H3T 1J4, Canada
Study Officials
- STUDY DIRECTOR
Issam Tanoubi, MD
Université de Montréal
- PRINCIPAL INVESTIGATOR
Marie-Eve Belanger, MD
Université de Montréal
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Université de Montréal
Study Record Dates
First Submitted
March 25, 2014
First Posted
April 7, 2014
Study Start
April 1, 2014
Primary Completion
August 1, 2014
Study Completion
August 1, 2014
Last Updated
December 2, 2014
Record last verified: 2014-12