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临床试验/NCT06140368
NCT06140368已完成不适用

The Effect of Virtual Reality on Pain, Anxiety and Patient Comfort During Trigger Point Injection

Izmir Bakircay University2 个研究点 分布在 1 个国家目标入组 84 人开始时间: 2023年5月10日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
84
试验地点
2
主要终点
State Anxiety Scale

研究概览

简要总结

To determine the effects of virtual reality application during trigger point injection on patients' pain, anxiety and comfort levels.This research was planned as a randomized controlled experimental type. The population of the research was planned to include patients who applied to the Algology polyclinic for trigger point injection. The sample of the research will consist of 150 patients who meet the sampling criteria and agree to participate in the research.Inclusion criteria: Trigger point injection applied for the first time, 18 years and over, understand and speak Turkish, understand verbal and written information given.Patients will be divided into two groups: experimental (virtual reality) and control groups.Data will be collected with the Case Report Form, State Anxiety Scale, General Comfort Scale and Visual Analog Scale.Patients' anxiety, comfort and pain levels will be evaluated before and after trigger point injection.

详细描述

Patients in the experimental group will be shown videos that the patient wants to watch, such as nature and seaside walks, underwater videos, with music background, through virtual reality glasses for 10 minutes.Patients in the control group will continue routine practice.Patients' anxiety, comfort and pain levels will be evaluated before and after trigger point injection.

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 (Care Provider)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • The procedure will be applied for the first time
  • 18 years and over
  • Able to understand and speak Turkish
  • Able to understand verbal and written information given
  • Having good cognitive abilities
  • Without visual or hearing loss
  • Patients who agreed to participate in the study

排除标准

  • Those who do not understand or speak Turkish
  • Does not understand verbal and written information
  • Those with impaired cognitive abilities

结局指标

主要结局

State Anxiety Scale

时间窗: 10 minutes after procedure

The scale developed by Spielberger et al. aims to measure state and trait anxiety levels separately.The scores obtained from the scale vary between 20-80, and the total score between 20-39 indicates mild anxiety, between 40-59 indicates moderate anxiety, and between 60-79 indicates severe anxiety.

General Comfort Scale

时间窗: 10 minutes after procedure

The scale, which was developed by Kolcaba in 2006 and has a total of 28 questions as 'Refreshing (9 items), Relaxation (9 items) and Overcoming Problems (10 items), consists of three sub-dimensions.The lowest value that can be taken is 1, which indicates low comfort, and the highest value, 6, indicates high comfort.

Visual Analog Scale

时间窗: In the middle (10 minutes) of the procedure

It is aimed to determine the level of pain.0 means no pain and 10 means maximum pain

次要结局

未报告次要终点

研究者

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

Elif Günay İsmailoğlu

Associate Professor

Izmir Bakircay University

研究点 (2)

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