AW&VR: Virtual Reality: a Teaching-learning Strategy for Cognitive Mastery in Airway Trauma Management

Sponsor
Sunnybrook Health Sciences Centre (Other)
Overall Status
Recruiting
CT.gov ID
NCT04451590
Collaborator
(none)
40
1
2
28
1.4

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Other: VR-based simulation
  • Other: Mannequin-based simulation
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (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.
Primary Purpose:
Other
Official Title:
Virtual Reality: a Teaching-learning Strategy for Cognitive Mastery in Airway Trauma
Actual Study Start Date :
Aug 1, 2021
Anticipated Primary Completion Date :
Sep 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: VR-based Simulation (Intervention)

Students will receive training on traumatic airway management using VR-based simulation.

Other: VR-based simulation
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.

Other: Mannequin-based Simulation (Control)

Students will receive training on traumatic airway management using mannequin-based simulation.

Other: Mannequin-based simulation
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.

Outcome Measures

Primary Outcome Measures

  1. Change in Traumatic Airway Injury Management Knowledge [up to 24 hours before and up to 24 hours after practice sessions]

    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).

  2. Application of Traumatic Airway Injury Management Knowledge [7 days after practice session]

    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

  1. Number of Required Practice Sessions [During the 1 day practice session]

    Identify whether VR or mannequin-based simulation practice require fewer practice sessions to achieve learning objectives.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sunnybrook Health Sciences Toronto Ontario Canada M4N 3M5

Sponsors and Collaborators

  • Sunnybrook Health Sciences Centre

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sunnybrook Health Sciences Centre
ClinicalTrials.gov Identifier:
NCT04451590
Other Study ID Numbers:
  • 108-2019
First Posted:
Jun 30, 2020
Last Update Posted:
Sep 5, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 5, 2021