The Impact of Virtual Reality Application on Pain, Anxiety, and Vital Parameters During Pleural Catheter Insertion: A Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 78
- 试验地点
- 2
- 主要终点
- Pain severity
研究概览
简要总结
The aim of this study is to examine the effects of virtual reality glasses applied to individuals who will undergo pleural catheter placement on pain, anxiety, and vital parameters. The main research questions that the study aims to answer are as follows:
- Does the application of virtual reality goggles have an effect on pain measured during pleural catheter insertion?
- Does the application of virtual reality goggles have an effect on anxiety measured during pleural catheter insertion?
- Does the application of virtual reality goggles have an effect on the vital parameters measured during pleural catheter insertion?
The researcher compared the intervention and control groups to determine whether the glasses have an effect on the measurable parameters (pain, anxiety, and vital signs).
详细描述
Today, both pharmacological and non-pharmacological methods are used to reduce patients' pain and anxiety during invasive procedures. Distraction techniques hold an important place among non-pharmacological methods. Virtual reality (VR) glasses can be effective in reducing perceived pain and anxiety by allowing patients to divert their attention elsewhere during procedures.
This study was conducted to evaluate the distribution of virtual reality brightness on patients' pain and anxiety levels.
The study was designed as a randomized controlled trial by the researchers. The patients included in the study were divided into two groups: the intervention group (exposed to virtual reality) and the control group (standard care). Following stratified randomization, randomization was carried out using a simple random number table.
Application:
During the insertion phase, Shinecon brand virtual reality glasses were placed on the patients during the connection process, and underwater images were shown.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Written or verbal consent to participate, Being over 18 years of age, Not having any psychiatric diagnosis, Not having any problems with vision, hearing, perception or communication.
排除标准
- •Being unconscious Experiencing pain due to any other problem
结局指标
主要结局
Pain severity
时间窗: From immediately before to 10 minutes after catheter insertion
Pain severity will be assessed using the Visual Analog Scale (VAS), a 10 cm scale ranging from 0 (no pain) to 10 (worst possible pain), measurements will be taken before, during and after pleural catheter insertion.
次要结局
- Anxiety level(From immediately before to 10 minutes after catheter insertion)
研究者
Almira Gurcan
Uzman hemşire, Adnan Menderes Üniversitesi, Cerrahi Hastalıkları Hemşireliği Anabilim Dalı
Aydin Adnan Menderes University