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Virtual Reality Simulation for Teaching and Assessment of Anesthesia Crisis Management

Virtual Reality Simulation for Teaching and Assessment of Anesthesia Crisis Management

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03434002
Enrollment
40
Registered
2018-02-15
Start date
2018-01-01
Completion date
2020-01-31
Last updated
2018-02-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patient Simulation

Keywords

Virtual Reality Simulation, Teaching and Assessment, Anesthesia Crisis Management

Brief summary

In this study, Investigators are going to develop and test a device to apply virtual reality simulation to improve and help for teaching and assessment of anesthesia crisis management.

Detailed description

Competency based medical education (CBME) is an outcomes-based approach to the design, implementation, assessment, and evaluation of medical education. The goals of Competency Based Medical Education are to improve patient safety, patient health outcomes, and enhance the competence and performance of individuals, groups and teams. Simulation-based training is a proven effective method to improve the skills and competency of the student by permit-ting repetitive practice before an actual procedure is performed on real patients. e Virtual reality simulation has been used successfully to teach technical skills such as laparoscopic surgery, carotid stenting, gall bladder surgery, and knee arthroscopy. The specific aims of this project are: 1. Build a multi-user, multi-site virtual reality simulator for anesthesia management and team training 2. Evaluate the simulation as a tool for competency based medical education 3. Compare the effectiveness of the simulator with mannequin based simulator for competency based medical education.

Interventions

OTHERTraining by Virtual Reality Simulation

Those Randomized 15 residents will be receive Local Anesthetic Systemic Toxicity simulation training by Virtual Reality simulation and after two weeks, they will be evaluated by investigators by using the same performance evaluation tool.

Randomized other 15 residents will be receive Local Anesthetic Systemic Toxicity simulation training by mannequin based simulation and after two weeks, they will be evaluated by investigators by using the same performance evaluation tool.

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
OTHER
Masking
NONE

Intervention model description

1. building the technical components for interaction within the virtual reality environment (phase 1); 2. application of this virtual reality in medical training (phase 2) and 3. measurement of training effectiveness with this Virtual Reality simulator against mannequin based training (phase 3).

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Anesthesia resident or fellow volunteers from University of Toronto

Exclusion criteria

* Unwilling to enter the study * Previous experience with simulator based teaching on local anesthetic systemic toxicity

Design outcomes

Primary

MeasureTime frameDescription
Number of tasks correctly performed1 hourThe primary outcome in performance evaluation is the number of tasks correctly performed during management of the Local Anesthetic Systemic Toxicity event. Investigators will use the same performance evaluation tool. The performance evaluation tool will assess the trainee's performance (i.e., medical management of Local Anesthetic Systemic Toxicity) per performance evaluation tool

Secondary

MeasureTime frameDescription
use the Anesthesiologists' Non-Technical Skills (ANTS) tool1 hourThe Investigators will use the anesthesiologists' non-technical skills (ANTS) tool in the Local Anesthetic Systemic Toxicity Event (Data Collection Tools, Supplemental Digital Content 2, http://links.lww.com/AAP/A45) as described by Neal.

Countries

Canada

Contacts

Primary ContactVincent Chan
vincent.chan@uhn.ca416-603-5118

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026