Effect of Virtual Reality on Patient Outcomes and Satisfaction in Total Knee Replacement

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorAykut Turgut

About this trial

This study aims to evaluate the effectiveness of virtual reality (VR) in managing preoperative anxiety and postoperative pain in patients undergoing total knee replacement. Investigators will assess the impact of preoperative VR training on anxiety levels, explore the effectiveness of relaxing and distracting VR videos for pain management after surgery, and determine the optimal timing for VR application by comparing different VR intervention times. Our goal is to identify how VR can improve both the emotional and physical recovery process for patients undergoing knee replacement surgery.

Eligibility criteria

Qualifiers

Patients with an ASA score of 1, 2, or 3

Elective unilateral total knee replacement surgery was planned,

Patients who are able to read and write in Turkish

Disqualifiers

Using >30 mg of oral oxycodone or equivalent daily

Long-term opioid use (>12 weeks)

Substance use disorder

Scheduled for emergency surgery

Trial design

Treatments tested in this trial

  • Virtual Reality Intervention for Preoperative Anxiety and Postoperative Pain Management (2 hours)
  • Device: Virtual Reality Intervention for Preoperative Anxiety and Postoperative Pain Management (4 hours)
  • Virtual Reality Intervention for Preoperative Anxiety and Postoperative Pain Management (6 hours)

Treatment groups

64 Participants
are divided into 4 treatment groups

Sponsors and collaborators

Aykut Turgut

Lead sponsor

Abant Izzet Baysal University

Sponsor institution