Recruiting

iVR & Mannequins

Sponsor:

The Ottawa Hospital

Code:

NCT07035015

Conditions

Nerve Block

Hip Fracture Surgeries

Eligibility Criteria

Sex: All

Age: 0+

Healthy Volunteers: Not accepted

Interventions

VR UGRA

Mannequin-based simulation

Study Details

Brief summary:

This research project aims to see if using immersive virtual reality (iVR) is as good as using traditional mannequins to teach medical staff how to perform a specific nerve block called an ultrasound-guided supra-inguinal fascia iliaca (SIFI) block. This nerve block is important for managing pain in patients with hip fractures, as it can improve recovery, shorten hospital stays, and reduce healthcare costs. Currently, not enough eligible hip fracture patients receive these beneficial nerve blocks.

The study will recruit 36 staff and trainees from anesthesiology, emergency medicine, and orthopedic surgery at The Ottawa Hospital. Participants will be randomly assigned to one of two groups. One group will learn the SIFI block using a newly developed iVR simulator that uses real human anatomy and allows for practice of needling and injecting. The other group will use traditional mannequin-based simulators.

All participants will receive educational materials and videos before their training. Their skills will be tested before the training, immediately after, and again one month later using a hybrid simulator (a combination of a mannequin and a soft embalmed human cadaver part). The main thing being measured is their skill level using a standardized scoring system. The study also wants to see if the iVR simulator is well-tolerated by users. The overall goal is to improve care for hip fracture patients through better, more accessible training for medical staff.

Conditions

Nerve Block

Hip Fracture Surgeries

Study ID

NCT07035015

Start date

Jun 1, 2025

Status verified date

Jun, 2025

Completion date

Nov, 2025

Anticipated

Primary completion date

Oct, 2025

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Staff and trainees from anesthesiology, emergency medicine, and orthopedic surgery. All participants will be locally recruited within The Ottawa Hospital

Study Design

Enrollment

36 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Other

Interventions and Outcome Measures

Arms

experimental: Virtual reality UGRA

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

active comparator: Mannequin simulation

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

Interventions

VR UGRA

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

Mannequin-based simulation

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

Primary outcome measure

  • Ultrasound Guided Regional Anesthesia Global Rating Scale [ Time Frame: From enrolment until the 1 month retention. ]

Central Contacts and Locations

Central contacts

Yuqi Gu, MD FRCPC

(613)737-8187yugu@toh.ca

Locations

The Ottawa Hospital

Recruiting

Ottawa, Ontario, Canada, K1H 8L6

Contacts

Yuqi Gu, MD FRCPC

(613)737-8187yugu@toh.ca

More Information

Sponsor

The Ottawa Hospital

Last update posted

Jun 24, 2025

Last verified

Jun, 2025

Keywords

  • Virtual Reality
  • Ultrasound-guided Regional Anesthesia
  • Simulation

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by The Ottawa Hospital on 2025-06-24.