Virtual Reality vs Mannequin for Ultrasound-Guided Nerve Block Teaching
This study compares the effectiveness of Virtual Reality and mannequin for teaching Ultrasound-Guided Nerve Block. The main outcome is assessed using the Ultrasound Guided Regional Anesthesia Global Rating Scale, where a higher score indicates better procedural performance.
VR UGRA
+ Mannequin-based simulation
Other Study
Summary
Study start date: June 1, 2025
Actual date on which the first participant was enrolled.This study aims to compare two different training methods for teaching medical professionals how to perform a specific type of anesthesia technique called the ultrasound-guided supra-inguinal fascia iliaca block, commonly used for pain relief in hip fractures. One method involves using immersive virtual reality (iVR) technology to simulate the human body and procedure, while the other uses traditional mannequin-based simulators. The study is important because it seeks to determine if the newer and potentially more accessible iVR method is as effective as the traditional approach, which could lead to more widespread use of this pain relief technique. It focuses on medical staff and trainees at The Ottawa Hospital who are involved in anesthesiology, emergency medicine, and orthopedics. Participants in the study are randomly assigned to either practice with the virtual reality system or the mannequin-based simulator after receiving the same educational materials. They practice the procedure for an hour and then are assessed on their skills before and after the training, as well as one month later, to see how well they retain the information. The study measures their performance using a scoring system and checks other factors like the time taken to complete the procedure and the number of attempts needed. For those using the virtual reality system, the study also looks at their experience with the technology, such as any feelings of dizziness or mental fatigue. The results of this study can help determine the most effective and user-friendly training method for this important medical procedure.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.36 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Other Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location