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Effect of Virtual Reality-Based Relaxation Exercise on Postoperative Pain and Kinesiophobia After Total Knee Replacement

Not Applicable
Active, not recruiting
Conditions
Randomized Controlled Trial
Interventions
Other: Exercise
Registration Number
NCT06591832
Lead Sponsor
Aksaray University
Brief Summary

The aim of this study is to evaluate the effect of virtual reality-based relaxation exercise on pain and kinesiophobia in patients after total knee arthroplasty.

Detailed Description

Virtual reality application, which is a non-pharmacological application; It is a three-dimensional simulation model that gives individuals the feeling of reality and allows mutual communication with a dynamic environment created by computers, and studies determining the effects of the application are increasing day by day. Virtual reality-based rehabilitation is a promising approach to achieve recovery in many cases, optimize functional outcomes, and increase the clinical and social benefits of surgery . As a result, pain and fear of movement may negatively affect early functional results in patients undergoing total knee arthroplasty. Explaining how to change patients' fears, encouraging them to adopt positive attitudes and increasing their physical strength has an important place in determining the effectiveness of virtual reality application.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
78
Inclusion Criteria
  • The research included people between the ages of 40-75,
  • Volunteering to participate in the research,
  • Being able to understand and speak Turkish,
  • Being able to understand the verbal, written and video explanations given,
  • Having no problems communicating cognitively, affectively and verbally,
  • Not having any obstacle to using virtual reality glasses,
  • Patients who underwent unilateral TKA surgery,
  • Using the SPH device at the same degree for three postoperative days after the FFP operation.
  • Having the surgeon's permission
Exclusion Criteria
  • Patients who will undergo revision TDP surgery,
  • Those who have a neurological disease that causes functional disability,
  • Those with a diagnosed psychiatric disorder,
  • Refusing to take the SPH device after the operation or taking it to a different degree,
  • Those who have a condition that prevents them from wearing virtual glasses for any reason,
  • These are patients after the FFP operation and outside the third postoperative day.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Experimental GorupExerciseRoutine nursing practice will be performed and Virtual reality based progressive relaxation exercise will be applied
Primary Outcome Measures
NameTimeMethod
Visual Analog ScaleMin 0 Max 10 (As the score increases, the pain increases.)

Visual Analog Scale

Tampa kinesiophobia scalemin 17 max 68 (As the score increases, the fear of movement increases.)

assesses fear of movement

Secondary Outcome Measures
NameTimeMethod
After application Visual Analog ScaleMin 0 Max 10 (As the score increases, the pain increases.)

Visual Analog Scale

After application Tampa kinesiophobia scalemin 17 max 68 (As the score increases, the fear of movement increases.)

assesses fear of movement

Trial Locations

Locations (2)

Aksaray Universitesi

🇹🇷

Aksaray, Turkey

Aksaray University

🇹🇷

Aksaray, Turkey

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