RA Anatomy - VRvST Study

Starting soon · Not applicable

Conditions studied: Virtual Reality Simulation, Virtual Reality, Education, Medical

In brief

Primary Objective: Score out of 44 on a validated test of anatomy and sono-anatomy Secondary Objective: Before training * Handedness (Edinburgh Handedness Inventory) * Subjective sleepiness (Karolinska scale) * Motor reaction time (Psychomotor Vigilance test) * Attention control (Anti-Saccade test) * Mental rotation (Mental Rotation Task) * Depression Anxiety, Stress (DASS score) * Visual Search Task (Divided Attention) * Knowledge pretraining After training and testing * Knowledge after training session * Acceptability: Client Satisfaction Questionnaire (CSQ-8) * Usability: CyberSickness in Virtual Reality Questionnaire (CSQ-VR) * Immersion: Witmer and Singer Presence Questionnaire * Subjective workload (NASA - TLX scale) * Cognitive Demand Battery (CBD) * Resource use: Calculation of cost differences between learning Modalities Study population: Resident anaesthetists Recruitment Target: 102 Methodology: This is a non-clinical randomised controlled trial of resident anaesthetists undergoing training in regional anaesthesia. Residents will be randomised to one of two groups for each training session day: * Standard anatomical training (Group A) * Virtual reality based anatomical training. (Group B) Then followed by another training day session and participants will enter either standard or VR teaching depending on the previous allocation: * Standard anatomical training (Group B) * Virtual reality based anatomical training. (Group A) Anatomical knowledge will be tested in both groups using an on-line questionnaire developed by the Chief Investigator. Eligibility criteria: Inclusion criteria: 1. Anaesthetists that are residents in a recognised Royal College of Anaesthetists (RCoA) training program 2. Anaesthetic training grades (Stage 1 - 3). Exclusion criteria: 1. Visual impairment (this does not include wearing glasses/contact lenses) 2. History of severe diseases affecting physical motion or balance 3. History of any drugs that may affect physical motion or balance within 12 hours of the intervention 4. Pregnancy 5. Individuals who had consumed alcohol within 24 h of the intervention. 6. Resident doctors not in a recognised RCOA training program e.g. Staff grade anaesthetists. Study treatment: Standard teaching - control Virtual reality teaching - intervention

Key facts

Study ID

NCT07361913

Run by

Royal National Orthopaedic Hospital NHS Trust

People needed

102

Starts

2026-01-01

Expected to finish

2027-01-31

Last updated by the study team

2026-01-23

Who can join

Age: any. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Anaesthetists that are residents in a recognised Royal College of Anaesthetists (RCoA) training program
• Anaesthetic training grades (Stage 1 - 3).

You may not qualify if…

• Visual impairment (this does not include wearing glasses/contact lenses)
• History of severe diseases affecting physical motion or balance
• History of any drugs that may affect physical motion or balance within 12 hours of the intervention
• Pregnancy
• Individuals who had consumed alcohol within 24 h of the intervention.
• Resident doctors not in a recognised RCOA training program e.g. Staff grade anaesthetists

Full record on ClinicalTrials.gov

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