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Effect of Virtual Reality Application Applied to Patients with Total Knee Replacement At Different Times

Not Applicable
Active, not recruiting
Conditions
Anxiety
Recovery Quality
Registration Number
NCT06792123
Lead Sponsor
Özge İşeri
Brief Summary

The aim of this study was to examine the effect of virtual reality application on anxiety and quality of recovery at different times (preoperatively and intraoperatively) in patients undergoing total knee replacement.

Detailed Description

The elderly population in the world and in our country is gradually increasing and the aging process is prolonged due to the prolongation of life expectancy. Osteoarthritis is one of the important obstacles limiting low quality of life and physical freedom in this aging process. It is estimated that osteoarthritis affects over 250 million people worldwide. Osteoarthritis is one of the important causes of severe pain and disability due to limitation of mobility, and this disease is a disease that causes deterioration in the psychological well-being of individuals and a low quality of life. The presence of symptoms characterized by joint pain, stiffness and limitation of movement in osteoarthritis negatively affects the quality of life of individuals. One of the most common problems in our country is osteoarthritis of the knee. In the treatment of osteoarthritis of the knee, total knee replacement surgery is performed as a last resort if pharmacologic and non-pharmacologic methods do not yield a positive response. Patients with total knee replacement may be exposed to anxiety and pain in this process. In previous studies, positive results were found when the effects of virtual reality application on pain were examined. The aim of this study was to examine the effect of virtual reality application on anxiety and quality of recovery at different times (preoperatively and intraoperatively) in patients undergoing total knee replacement. In previous studies, it was determined that virtual reality application was mostly applied preoperatively and examined pain and vital signs. There are no studies on quality of recovery

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
120
Inclusion Criteria
  • Over the age of 18
  • No psychiatric medication
  • No mental and cognitive disabilities
  • Those who underwent Total Knee Replacement,
Exclusion Criteria
  • Patients with visual and hearing impairment
  • Receiving general anesthesia
  • Experiencing complications during surgery

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
AnxietyPre-test before surgery; post-test two hours after surgery

Beck Anxiety Scale

Recovery qualityPre-test before surgery; post-test two hours after surgery

quality of recovery-15 (QoR-15)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Ondokuz Mayıs Unıversity

🇹🇷

Samsun, Atakum, Turkey

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