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
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Score out of 44 on a validated test of anatomy and sono-anatomy
Timeframe: From enrolement to end of study day 2