Effectiviteit van Virtual Reality op de pijn en angst beleving na een totale knie of heup prothese operatie
- Conditions
- Patients who fulfill the inclusion criteria and receive elective orthopedic surgery (total hip OR total knee replacement)
- Registration Number
- NL-OMON24456
- Lead Sponsor
- one
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
•Written and orally given informed consent
•18 years and older
•Proficient in Dutch
•Indication for elective total hip or total knee replacement surgery under spinal anesthesia
•Medically cleared for participation by the surgeon
Exclusion Criteria
•Chronical use of pain medication (opioids)
•Known motion sickness
•Epileptic insults in previous history
•Claustrophobic
•Blindness
•Incapacity to follow the protocol.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint of this study is to evaluate the effect of VR on pain sensation as measured with the NRS for pain after orthopeadic hip and knee arthroplasty compared to standard care .
- Secondary Outcome Measures
Name Time Method The secondary endpoints of this study are to evaluate the effect of VR on anxiety scores, Pain Catastrophizing Scale (PCS), analgesic use (peri- and post-operative, daily use of paracetamol, NSAIDs, opioids), length of hospital stay. In addition, we will assess tolerability, feasibility and satisfaction of VR use.