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临床试验/NCT06550323
NCT06550323Enrolling By Invitation不适用

Göğüs Tüpü Çıkarma İşlemi Sırasında Sanal Gerçeklik Uygulamasının Ağrı, Anksiyete ve Konfora Etkisi

Hale Rumeysa Seçer2 个研究点 分布在 2 个国家目标入组 82 人开始时间: 2023年3月20日最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
82
试验地点
2
主要终点
State-Trait Anxiety Inventory Scale

研究概览

简要总结

Chest tubes are used to eliminate possible acute or chronic problems that may occur after trauma or surgical interventions to the chest area. This process, which aims to drain the fluid, blood or air accumulated in the pleural area, works with the support of closed underwater drainage systems. The chest tubes, which remain in place for a long time, fuse with the endothelium lying in the chest cavity. For this reason, the adhesions formed with the fusion cause very severe acute pain in the patient with the pulling force applied during removal.The high level of pain of the person will cause an increase in the level of anxiety and a decrease in the level of comfort. The anxiety experienced by the patients will also reduce the tolerance to pain.It has been observed that the use of virtual reality in the field of health significantly reduces the level of pain and anxiety during medical procedures, shortens wound healing and hospital stay, and increases compliance with treatment.In the literature, no studies were found in which the effects of virtual reality application on pain, anxiety and comfort were evaluated in patients whose chest tube was removed.Thereforee, this study was conducted to evaluate the effect of virtual reality application against all these negative situations.

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
Double (Participant, Investigator)

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

  • Must be between the ages of 18-65,
  • Must have undergone coronary artery bypass graft surgery and have a chest tube,
  • Must participate in the study voluntarily,
  • Must not have vision or hearing problems,
  • Must not have disorientation in place and time,
  • Must not have any psychiatric disorders,

排除标准

  • Those with chronic pain and routinely using painkillers,
  • Those using painkillers before the procedure,
  • Those with problems such as migraine, vertigo, dizziness,
  • Patients using prescription glasses and those having vision problems without glasses were not included in the study.

结局指标

主要结局

State-Trait Anxiety Inventory Scale

时间窗: 5 month

It is a 4-point Likert-type scale with 40 items and is scored as "never": 1, "a little": 2, "a lot": 3, "completely": 4, according to the degree of severity of the feelings, thoughts or behaviors expressed by the items. anxiety level will be determined.

comfort scale

时间窗: 5 month

It is a scale ranging from 0 to 10 points. While 0 points indicate 'most comfortable', 10 points indicate 'most uncomfortable'. The minimum value is 0 and the maximum value is 10. 0 represents a good result and 10 represents a bad result

visual analog scale

时间窗: 5 month

To evaluate pain severity, pain results are evaluated by scoring between 0-10. While 0 indicates "No pain", 10 indicates "Unbearable pain". The minimum value is 0 and the maximum value is 10. 0 represents a good result and 10 represents a bad result

verbal pain scale

时间窗: 5 month

0 points indicate "No pain", 1 point indicates "Mild pain", 2 points indicate "Moderate pain" and 3 points indicate "Severe pain".

次要结局

未报告次要终点

研究者

发起方
Hale Rumeysa Seçer
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Hale Rumeysa Seçer

Nurse

Ataturk University

研究点 (2)

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