Joint replacement surgery in elderly patients with severe osteoarthritis of the hip or knee: decision making, postoperative recovery, and clinical outcomes.
Mary Beth Hamel, Maria Toth, Anna Legedza...
https://pubmed.ncbi.nlm.nih.gov/18625924Actively Recruiting
Led by Belfast Health and Social Care Trust · Updated on 2025-05-08
40
Participants Needed
1
Research Sites
N/A
Total Duration
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
Can the Use of Virtual Reality Improve TKA Outcomes
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
Total: 1 location
1
Musgrave Park Hospital
Belfast, United Kingdom
Actively Recruiting
N
Nicola Gallagher
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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