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临床试验/NCT06458647
NCT06458647已完成不适用

Effect of Virtual Reality Video Viewing Before Coronary Angiography on Anxiety, Comfort, and Patient Satisfaction

TC Erciyes University1 个研究点 分布在 1 个国家目标入组 74 人开始时间: 2024年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
74
试验地点
1
主要终点
Patient satisfaction

研究概览

简要总结

This study was planned as a randomized controlled experimental study to examine the effects of virtual reality video on anxiety, comfort and patient satisfaction before coronary angiography. Data will be collected using the Descriptive Characteristics Questionnaire, State-Trait Anxiety Inventory, Early Postoperative Comfort Scale, Visual Analog Scale (VAS) for patient satisfaction and pain, Vital Signs Follow-up Form and Complication Follow-up Form.

详细描述

This study was planned as a randomized controlled experimental study to examine the effects of virtual reality video on anxiety, comfort and patient satisfaction before coronary angiography. Data will be collected using the Descriptive Characteristics Questionnaire, State-Trait Anxiety Inventory, Early Postoperative Comfort Scale, Visual Analog Scale (VAS) for patient satisfaction and pain, Vital Signs Follow-up Form and Complication Follow-up Form. In addition to the standard practices of the clinic, individuals in the intervention group will be shown a video with virtual reality glasses before entering the angiography procedure. Only standard practices of the clinic will be applied to the control group.

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
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

入选标准

  • Can speak and understand Turkish,
  • Over 18 years of age,
  • No previous angiography procedure,
  • Oriented to place and time,
  • No psychiatric illness,
  • Not taking any sedative medication,
  • No vision and hearing problems,
  • Patients who volunteered to participate in the study will be included.

排除标准

  • Patients with any pain or chronic pain prior to coronary angiography,
  • Patients diagnosed with anxiety,
  • Patients with pacemakers,
  • Patients requiring emergency angiography,
  • Patients taking antihistamines and psychiatric drugs,
  • Patients who did not volunteer to participate in the study,
  • Patients taking tranquilizers or pain medication up to 5 hours before the angiography procedure were excluded.

研究组 & 干预措施

Intervention group

Experimental

Individuals in the intervention group will be shown a video with virtual reality glasses before entering the angiography procedure.

干预措施: Video Streaming with Virtual Reality (Other)

Control group

No Intervention

No application will be made to the control group before the procedure.

结局指标

主要结局

Patient satisfaction

时间窗: 30 minutes after angiography

Patients will be asked to rate their satisfaction with the intervention on a 10-point scale.

Anxiety

时间窗: 30 minutes after angiography

This inventory, which consists of a total of 40 items, is analyzed in two separate sections: The first part is the State Anxiety Inventory, which consists of 20 items, and the individual answers this section with his/her current feelings. The second part is the Trait Anxiety Inventory, which also consists of 20 items, and the individual answers this section with the feelings they have felt in the last 7 days.

Comfort

时间窗: 30 minutes after angiography

The scale, which is based on the concept of comfort, consists of a total of 24 items, 12 of which question the comfort status of the individual before and after the surgical intervention, 12 of which question positive and 12 of which question negative experiences.

次要结局

  • Comfort(30 minutes after angiography)
  • Patient satisfaction(30 minutes after angiography)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sevda Korkut

Associate Prof.

TC Erciyes University

研究点 (1)

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