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Clinical Trials in Turkey / NCT06933732
Starting soon Not applicable

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

NCT06933732 · tracked via the Priya Life Science Turkey tracker
Sponsor
Aykut Turgut
Phase
Not applicable
Started
2025-12-25
Last updated
2025-09-26

Condition(s) studied

Knee ReplacementKnee Replacement SurgeryPostoperative Pain, AcuteAnxiety, PreoperativePain ManagementVirtual Reality

Investigational drug(s) / intervention(s)

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)

Virtual Reality Intervention for Preoperative Anxiety and Postoperative Pain Management (2 hours): The Virtual Reality intervention involves participants wearing a VR headset at least one hour prior to their surgery to watch immersive, pre-recorded educational videos showing the operating room with a nurse explaining the process aimed at reducing pre-operative anxiety and nature videos with distraction effect after surgery for pain management. The intervention for pain management will be delivered 2 hours after surgery. The videos to be shown to patients will be limited to a maximum of 30 minutes. In addition, all participants will be reminded that they can remove the glasses or leave the study at any time.

Device: Virtual Reality Intervention for Preoperative Anxiety and Postoperative Pain Management (4 hours): The Virtual Reality intervention involves participants wearing a VR headset at least one hour prior to their surgery to watch immersive, pre-recorded educational videos showing the operating room with a nurse explaining the process aimed at reducing pre-operative anxiety and nature videos with distraction effect after surgery for pain management. The intervention for pain management will be delivered 4 hours after surgery. The videos to be shown to patients will be limited to a maximum of 30 minutes. In addition, all participants will be reminded that they can remove the glasses or leave the study at any time.

Virtual Reality Intervention for Preoperative Anxiety and Postoperative Pain Management (6 hours): The Virtual Reality intervention involves participants wearing a VR headset at least one hour prior to their surgery to watch immersive, pre-recorded educational videos showing the operating room with a nurse explaining the process aimed at reducing pre-operative anxiety and nature videos with distraction effect after surgery for pain management. The intervention for pain management will be delivered 6 hours after surgery. The videos to be shown to patients will be limited to a maximum of 30 minutes. In addition, all participants will be reminded that they can remove the glasses or leave the study at any time.

Study summary

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

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * 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 Exclusion Criteria: * Using \>30 mg of oral oxycodone or equivalent daily * Long-term opioid use (\>12 weeks) * Substance use disorder * Scheduled for emergency surgery * Scheduled for revision surgery * Requiring postoperative intensive care * Patients with visual or hearing impairments * Individuals experiencing motion-related nausea or dizziness * History of stroke or dementia * Pregnant or breastfeeding women * Patients with a history of epilepsy or seizures

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Aibu Izzet Baysal Training and Research Hospital Bolu Turkey (Türkiye)

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06933732 on ClinicalTrials.gov ↗ ← All trials in Turkey