Actively Recruiting

Phase Not Applicable
Age: 18Years - 100Years
All Genders
ID06962046

Can the Use of Virtual Reality Improve Outcomes Following Total Knee Arthroplasty With Spinal Anaesthesia? - A Pilot Study

Led by Belfast Health and Social Care Trust · Updated on 2025-05-08

40

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research evaluates the use of virtual reality (VR) alongside spinal anaesthesia during total knee arthroplasty (TKA). The study aims to determine if VR can reduce the need for deeper sedation while maintaining patient satisfaction and potentially lowering side effects commonly linked to sedation such as nausea, confusion, and breathing difficulties. It also explores the feasibility and outcomes of VR use in this surgical setting. Participants will all receive spinal anaesthesia. They are randomly assigned to one of two groups: one group will use VR combined with light sedation, while the other group will receive standard care with deeper sedation but no VR. The study compares these approaches to assess if VR can help reduce sedation dosage and related side effects during TKA. During the study, patients will be monitored for sedation levels, recovery quality, and complications up to one week after surgery. Researchers will assess various outcomes including sedation amount, cognitive tests, mobilization time, pain management, anti-nausea medicine use, and hospital stay length. The primary outcome is to evaluate the feasibility of using VR during TKA with spinal anaesthesia, measured the day after surgery.

CONDITIONS

Brief Title

Can the Use of Virtual Reality Improve TKA Outcomes

Who Can Participate

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 18 years or older
  • Patients classified as American Society of Anaesthesiologists (ASA) grade 1 or 2
  • Scheduled for routine primary elective knee arthroplasty
Not Eligible

You will not qualify if you...

  • Patients classified as ASA grade 3 or 4
  • Patients unable to use VR, such as those with dementia
  • Patients with an existing diagnosis of delirium
  • Patients with visual impairment exceeding the corrective power of the VR headset
  • Patients who use hearing aids
  • Patients with a history of motion sickness
  • Patients with epilepsy, history of blackouts, or seizures
  • Patients undergoing operations expected to last over 1 hour or requiring complex surgery
  • Patients who have requested no sedation during the operation
  • Patients who have received premedication
  • Patients undergoing general anaesthesia
  • Patients who do not understand verbal or written English or have special communication needs
  • Patients not capable of giving informed consent

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Day of surgery

Participants undergo total knee arthroplasty with spinal anaesthesia and limited propofol sedation, with or without virtual reality during surgery.

1 surgical visit

Post-operative Follow-up

Duration - Up to 1 week post operation

Participants are observed and assessed for recovery quality, sedation effects, complications, and mobilisation following surgery.

Several visits including assessments at 1 hour, 4 hours, 24 hours, and 48 hours after surgery, plus monitoring up to 1 week

Trial Site Locations

Total: 1 location

1

Musgrave Park Hospital

Belfast, United Kingdom

Actively Recruiting

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Research Team

N

Nicola Gallagher

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Peter Y Chan, Simon Scharf

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