NCT05755724

Brief Summary

Patients in rural Canada face serious anesthesia care deficiencies relative to their counterparts in urban centers. Despite 18% of Canadians living in rural settings only 3.1% of medical specialists practice in rural areas. To provide equity in healthcare there is a need to develop a network where specialists in urban centers can provide training, coaching, and support to physicians in rural communities. Despite some work being done this is not possible for all specialists due to cost and travel. One potential solution to this problem is telesimulation, whereby telecommunication and simulation tools are used to provide training remotely. Simple, 2D telesimulation setups using webcams and computers have been used to teach remotely but problems with video displays and learner engagement have occurred leading to a need for more sophisticated telesimulation tools. Recently, virtual reality (VR) systems have been developed allowing the learner and teacher to immerse in a 3D computer-generated environment where they feel as if they are in the same room. We propose to see whether teaching ultrasound guided regional anesthesia (UGRA), a skill required by rural physicians, using 3D VR is better than teaching by 2D tele simulation.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
24

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2023

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 11, 2023

Completed
Same day until next milestone

Study Start

First participant enrolled

February 11, 2023

Completed
23 days until next milestone

First Posted

Study publicly available on registry

March 6, 2023

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2024

Completed
Last Updated

August 23, 2024

Status Verified

August 1, 2024

Enrollment Period

1.4 years

First QC Date

February 11, 2023

Last Update Submit

August 22, 2024

Conditions

Keywords

Regional AnesthesiaEducationUltrasound

Outcome Measures

Primary Outcomes (2)

  • 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) will be assessed using a validated procedural checklist termed as the Assessment Checklist for Ultrasound-Guided Regional Anesthesia. The checklist has 22 items which will be graded as not performed (0 Marks), performed poorly (1 Mark), or performed well (2 Marks).

    15 minutes

  • Difference in scores from before (pretest) to after training (posttest) using an Global Rating Scale (GRS) for assessment of Ultrasound Guided Regional Anesthesia.

    Difference in scores from before (pretest) to after training (posttest) will be assessed using a validatedGlobal Rating Scale termed as the Global Rating Scale (GRS) for assessment of Ultrasound Guided Regional Anesthesia.The GRS has 9 items with a score of 1-5 for each item, with 1 correlating to a very poor performance and 5 correlating to a clearly superior performance.

    15 minutes

Secondary Outcomes (2)

  • Qualitative assessment of teacher and student satisfaction for each modality

    10 minutes

  • Time required to teach UGRA using each modality

    10 minutes

Study Arms (2)

Remote immersive virtual reality group (3D) teaching

EXPERIMENTAL

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.

Other: 3-D Teaching

Remote 2 D teaching

PLACEBO COMPARATOR

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).

Other: 2-D Teaching

Interventions

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.

Also known as: Remote immersive virtual reality group (3D) teaching
Remote immersive virtual reality group (3D) teaching

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).

Also known as: Remote 2 D Teaching
Remote 2 D teaching

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Participants are medical students from year 1 and 2

You may not qualify if:

  • Participants with any prior exposure (workshop, lecture, tutorial, actual performance) of ultrasound guided procedures, including regional anesthesia.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sunnybrook Health Sciences Centre

Toronto, Ontario, M4N 3M5, Canada

Location

MeSH Terms

Conditions

Acute Pain

Interventions

Educational Status

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Socioeconomic FactorsPopulation Characteristics

Study Officials

  • Ahtsham U Niazi, FRCPC

    Sunnybrook Health Sciences Centre

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Masking Details
Double blinded
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: The study will be designed as a single-centre, prospective, double blinded, randomized (1:1) trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

February 11, 2023

First Posted

March 6, 2023

Study Start

February 11, 2023

Primary Completion

June 30, 2024

Study Completion

June 30, 2024

Last Updated

August 23, 2024

Record last verified: 2024-08

Locations