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Virtual Reality Teaching for Anesthesia Training (RIVR Trial)
N/A
Recruiting
Led By Ahtsham U Niazi, FRCPC
Research Sponsored by Sunnybrook Health Sciences Centre
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Participants are medical students from year 1 and 2
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 15 minutes
Awards & highlights
RIVR Trial Summary
This trial aims to see if using 3D virtual reality is better than 2D tele-simulation to train rural physicians in providing anesthesia care.
Who is the study for?
This trial is for first and second-year medical students who have not had any previous experience with ultrasound-guided procedures, including regional anesthesia. It's designed to help those in rural Canada where there's a shortage of medical specialists.Check my eligibility
What is being tested?
The study is testing whether teaching ultrasound guided regional anesthesia (UGRA) through immersive 3D Virtual Reality (VR) systems is more effective than traditional 2D tele simulation methods used for remote education.See study design
What are the potential side effects?
Since this trial involves educational techniques rather than medications, typical drug side effects are not applicable. However, participants may experience discomfort or dizziness associated with VR technology.
RIVR Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am a first or second-year medical student.
RIVR Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 15 minutes
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~15 minutes
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Difference in scores from before (pretest) to after training (posttest) using an Assessment Checklist for Ultrasound-Guided Regional Anesthesia.
Difference in scores from before (pretest) to after training (posttest) using an Global Rating Scale (GRS) for assessment of Ultrasound Guided Regional Anesthesia.
Secondary outcome measures
Qualitative assessment of teacher and student satisfaction for each modality
Time required to teach UGRA using each modality
RIVR Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Remote immersive virtual reality group (3D) teachingExperimental Treatment1 Intervention
Telesimulation using immersive VR technology. Briefly, students will have a 360° camera mounted to their head, which will broadcast their first-person perspective to their teachers. Teachers will be able to immerse themselves in the perspective of the trainee using a virtual reality HMD (Oculus Quest 2), which allows them to look around freely and view equipment, hand movements, etc. and offer instruction accordingly.
Group II: Remote 2 D teachingPlacebo Group1 Intervention
Telesimulation using standard teleconferencing software and equipment including 2D computer monitors, webcams, and an ultrasound machine linked to a computer (enabling ultrasound images to be transmitted).
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Who is running the clinical trial?
Sunnybrook Health Sciences CentreLead Sponsor
656 Previous Clinical Trials
1,551,284 Total Patients Enrolled
3 Trials studying Acute Pain
2,274 Patients Enrolled for Acute Pain
Ahtsham U Niazi, FRCPCPrincipal InvestigatorSunnybrook Health Sciences Centre
1 Previous Clinical Trials
40 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I am a first or second-year medical student.I have experience with ultrasound-guided procedures.
Research Study Groups:
This trial has the following groups:- Group 1: Remote immersive virtual reality group (3D) teaching
- Group 2: Remote 2 D teaching
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there any vacancies for the clinical trial at this time?
"Affirmative. Per the information published on clinicaltrials.gov, this medical study was initially posted on February 11th 2023 and is currently recruiting patients. 24 participants need to be identified from a single location."
Answered by AI
To what capacity is this trial accepting participants?
"Yes, according to clinicaltrials.gov this study is currently open for enrolment - the original advertisement was posted on February 11th of 2023 and last amended on March 2nd of 2023. Participation requires 24 patients across a single centre."
Answered by AI
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