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临床试验/NCT06591832
NCT06591832进行中(未招募)不适用

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

Aksaray University3 个研究点 分布在 1 个国家目标入组 78 人开始时间: 2024年1月15日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
78
试验地点
3
主要终点
Visual Analog Scale

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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.

结局指标

主要结局

Visual Analog Scale

时间窗: Min 0 Max 10 (As the score increases, the pain increases.)

Visual Analog Scale

Tampa kinesiophobia scale

时间窗: min 17 max 68 (As the score increases, the fear of movement increases.)

assesses fear of movement

次要结局

  • After application Visual Analog Scale(Min 0 Max 10 (As the score increases, the pain increases.))
  • After application Tampa kinesiophobia scale(min 17 max 68 (As the score increases, the fear of movement increases.))

研究者

发起方
Aksaray University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Zeynep Kocak

Principal Investigator

Aksaray University

研究点 (3)

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