Virtual Reality: a Teaching-learning Strategy for Cognitive Mastery in Airway Trauma Management (AW&VR)
Primary Purpose
Education, Medical, Airway Management, Students, Medical
Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
VR-based simulation
Mannequin-based simulation
Sponsored by
About this trial
This is an interventional other trial for Education, Medical
Eligibility Criteria
Inclusion Criteria:
- Age ≥18 at time of consent
- Medical student at U of T in 1st, 2nd or 3rd year
- Able to attend two sessions a week apart
Exclusion Criteria:
- Lack of participant consent or capacity to give consent
- History of significant motion sickness (during exposure to physical, visual and virtual motion, cybersickness verbally declared by patient)
- Visual/hearing impairments that affect abilities to listen/watch videos/VR video
Sites / Locations
- Sunnybrook Health SciencesRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
VR-based Simulation (Intervention)
Mannequin-based Simulation (Control)
Arm Description
Students will receive training on traumatic airway management using VR-based simulation.
Students will receive training on traumatic airway management using mannequin-based simulation.
Outcomes
Primary Outcome Measures
Change in Traumatic Airway Injury Management Knowledge
Knowledge acquisition of traumatic airway injury management as assessed by the written Key Features Decision Making Checklist, Change from baseline (pre-training) knowledge to after practice session knowledge (post-training).
Application of Traumatic Airway Injury Management Knowledge
Application of decision making concepts surrounding traumatic airway injury management as assessed by the Airway Injury Checklist of Core Decision Making Steps completed during participant performance of a simulated crisis assessment scenario.
Secondary Outcome Measures
Number of Required Practice Sessions
Identify whether VR or mannequin-based simulation practice require fewer practice sessions to achieve learning objectives.
Full Information
NCT ID
NCT04451590
First Posted
November 12, 2019
Last Updated
September 12, 2022
Sponsor
Sunnybrook Health Sciences Centre
1. Study Identification
Unique Protocol Identification Number
NCT04451590
Brief Title
Virtual Reality: a Teaching-learning Strategy for Cognitive Mastery in Airway Trauma Management
Acronym
AW&VR
Official Title
Virtual Reality: a Teaching-learning Strategy for Cognitive Mastery in Airway Trauma
Study Type
Interventional
2. Study Status
Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
August 1, 2021 (Actual)
Primary Completion Date
September 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sunnybrook Health Sciences Centre
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Airway injury in patients is a high risk and complex medical crisis. Unfortunately, training for airway management in injured patients is challenging. The most effective way of practicing airway management is using mannequins. However, mannequin training is expensive and only occasionally available to medical trainees.
The purpose of this study is to determine if Virtual Reality (VR) can be used to educate medical students on airway injury management. VR training will involve managing the care of a patient with an airway injury in an immersive, interactive VR hospital trauma bay. The investigators will compare the knowledge gained from VR training vs. mannequin training. The investigators will also investigate whether VR training teaches students faster than mannequin training. In addition, the investigators will identify factors which might affect learning from VR.
Medical students who choose to participate will be randomized (i.e. participant will have a 50% chance to be placed in either group) to be trained with VR or a mannequin. Participants then will be trained on airway injury management using their assigned training approach. One week later, all participants will be assessed on their airway injury management skills using a mannequin. Before and after their sessions, participants will also be asked to complete a questionnaire on their clinical decision-making. Participants who received VR training will also complete a questionnaire about their experience with the VR training.
This study will help develop a new approach to airway management training which is cheaper and more easily available to medical trainees than mannequin training. This educational tool could lead to better treatment of airway trauma in future patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Education, Medical, Airway Management, Students, Medical, Virtual Reality, Trauma Centers, Manikins
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
An external assessor will score videos participants performing Airway Trauma Management using the Airway Injury Checklist on Core Decision Making Steps. The assessors will be blinded to intervention.
Allocation
Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
VR-based Simulation (Intervention)
Arm Type
Experimental
Arm Description
Students will receive training on traumatic airway management using VR-based simulation.
Arm Title
Mannequin-based Simulation (Control)
Arm Type
Other
Arm Description
Students will receive training on traumatic airway management using mannequin-based simulation.
Intervention Type
Other
Intervention Name(s)
VR-based simulation
Intervention Description
Participants will experience a novel interactive and immersive VR full size trauma bay with an adult patient and healthcare professionals. Immersed in the environment, learners undertake the decision-making steps in managing the medical care for a patient with an airway injury. Learners are first given the case scenario from which they form their own learning goals/plans. They then navigate through the scenario that will provide feedback depending on their actions in the form of either the patient's hemodynamic changes or prompts from healthcare avatars in the scenario. These feedback processes are built-in and designed to promote reflection and reorganization of the learner's decision-making strategies. As learning progresses, fewer prompts will be given. At the end of the scenario, evaluation algorithms pre-programmed into the VR-based simulation will be displayed.
Intervention Type
Other
Intervention Name(s)
Mannequin-based simulation
Intervention Description
Participants will experience a mannequin-based scenario practice which is the current gold standard in medical education. The trauma airway management scenario will match the VR environment and sequence of events.
Primary Outcome Measure Information:
Title
Change in Traumatic Airway Injury Management Knowledge
Description
Knowledge acquisition of traumatic airway injury management as assessed by the written Key Features Decision Making Checklist, Change from baseline (pre-training) knowledge to after practice session knowledge (post-training).
Time Frame
up to 24 hours before and up to 24 hours after practice sessions
Title
Application of Traumatic Airway Injury Management Knowledge
Description
Application of decision making concepts surrounding traumatic airway injury management as assessed by the Airway Injury Checklist of Core Decision Making Steps completed during participant performance of a simulated crisis assessment scenario.
Time Frame
7 days after practice session
Secondary Outcome Measure Information:
Title
Number of Required Practice Sessions
Description
Identify whether VR or mannequin-based simulation practice require fewer practice sessions to achieve learning objectives.
Time Frame
During the 1 day practice session
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Age ≥18 at time of consent
Medical student at U of T in 1st, 2nd or 3rd year
Able to attend two sessions a week apart
Exclusion Criteria:
Lack of participant consent or capacity to give consent
History of significant motion sickness (during exposure to physical, visual and virtual motion, cybersickness verbally declared by patient)
Visual/hearing impairments that affect abilities to listen/watch videos/VR video
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Alam Fahad, MD, M.Sc
Phone
416-480-4864
Ext
4798
Email
fahad.alam@sunnybrook.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Lilia Kaustov, PhD
Phone
416-480-6100
Ext
89607
Email
lilia.kaustov@sunnybrook.ca
Facility Information:
Facility Name
Sunnybrook Health Sciences
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4N 3M5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fahad Alam, MD
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Virtual Reality: a Teaching-learning Strategy for Cognitive Mastery in Airway Trauma Management
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