Virtual Reality During Passive Motion After Knee Surgery

Sponsor
Manisa Celal Bayar University
Study ID
NCT07177573
Status
Not Yet Recruiting

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Conditions

  • Total Knee Arthroplasty

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Virtual Reality — OTHER
    The demographic information of the participants will be collected through face-to-face interviews. Pain and comfort levels will be assessed using the Visual Analog Scale (VAS) prior to the intervention. Additionally, anxiety levels will be measured with the Spielberger State-Trait Anxiety Inventory, and vital signs will be recorded. Patients included in the study will be informed about the use of virtual reality (VR) goggles and introduced to the videos that will be viewed. During the Continuous Passive Motion (CPM) application, patients will be positioned in a semi-Fowler's position with a pillow placed under the head for support. Through virtual reality, patients will watch the video Forest Walk along the Middle Fork Snoqualmie River Trail with Relaxing Sounds and the accompanying sounds will be delivered through headphones integrated into the goggles.

Study Details

The purpose of this study is to investigate the effects of virtual reality on pain, anxiety, and comfort during continuous passive motion following total knee arthroplasty

Key Dates

First listed
Sep 17, 2025
Start date
Sep 30, 2025
Status verified
Sep 2025
Primary completion
Oct 1, 2026
Completion
Oct 1, 2026

Study Design

Enrollment
102 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE

Arms

  • Experimental: Experimental
    Virtual Reality
  • No Intervention: Control

Primary Outcome Measure

Pain, Anxiety, and Comfort Levels during Continuous Passive Motion [ Time Frame: Immediately before and after each CPM session on postoperative day 2 and day 3 ]

Central Contacts

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