Recruiting

Virtual Reality vs Mannequin for Ultrasound-Guided Nerve Block Teaching

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Study Aim

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.

What is being tested

VR UGRA

+ Mannequin-based simulation

Other
Who is being recruted

1 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Other Study

Interventional
Study Start: June 2025
See protocol details

Summary

Principal SponsorThe Ottawa Hospital
Study ContactYuqi Gu, MD FRCPC
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitleSelf-Guided Immersive Virtual Reality Versus Mannequin-based Simulators to Teach the Ultrasound-Guided Supra-Inguinal Fascia Iliaca Block: A Non-inferiority Randomized Controlled Study
NCT07035015
Principal SponsorThe Ottawa Hospital
Study ContactYuqi Gu, MD FRCPC
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

36 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Other Study

Some studies explore topics that don't fall into a specific category. These might include innovative research, new technologies, or emerging healthcare areas.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

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

1 inclusion criteria required to participate
Staff and trainees from anesthesiology, emergency medicine, and orthopedic surgery. All participants will be locally recruited within The Ottawa Hospital

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
The simulator applied principles of cognitive task analysis, which is a method aimed at describing the knowledge, cognitive process, and goal structures experts rely upon while performing a complex procedure

Group II

Active Comparator
The hybrid simulator will consist of a 3G mannequin and a gel-based part-task trainer.

Study 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

Recruiting

The Ottawa Hospital

Ottawa, CanadaOpen The Ottawa Hospital in Google Maps
Recruiting
One Study Center
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