The Effect of Virtual Reality Glasses Applied on Chest Tube Removal After Open Heart Surgery on Pain Level and Hemodynamic Variables
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 82
- 试验地点
- 2
- 主要终点
- Pain evaluated using the Visual Analogue Scale
研究概览
简要总结
In this study, between 1 January 2025 - 1 June 2025, who met the inclusion and exclusion criteria, a total of 82 patients who are on the 2nd or 3rd day after the surgery and who are hospitalized in the cardiovascular surgery intensive care clinic will be recruited.
详细描述
The patient will be put on virtual reality glasses five minutes before the chest tube is removed. Afterwards, it will continue to be watched while the tube is taken and virtual reality glasses will be watched for another five minutes. Pain level and hemodynamic variables will be checked before, during, and 15 and 30 minutes after virtual reality glasses are watched. The participants in the control group will receive routine treatment and care, and their data will be collected at the same time as those in the study group. Hemodynamic variables will be monitored and recorded on the monitor.
Virtual reality glasses application is a method without any side effects. During the research, any adverse condition (vision problem, nausea, dizziness, etc.) related to the use of virtual glasses will be observed by the researcher. Since virtual reality glasses will be used in another patient after being used on one patient, disinfection will be made in line with the company's recommendations, taking into account the pandemic conditions. Throughout the application, feedback will be received from the patients by the researchers.
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
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Agreeing to participate in the research (signing the Informed Consent Form),
- •Conscious and cooperative,
- •Stable hemodynamic status,
- •Speaks and understands Turkish,
- •Over 18 years old,
- •On the 2nd and 3rd day after open heart surgery,
- •Having chest tube,
- •No sensitivity or trauma in the area (for the study group) where the virtual reality glasses will be applied,
- •No active COVID-19 infection,
- •Patients without any psychiatric diagnosis
排除标准
- •Agreeing to participate in the research (signing the Informed Consent Form),
- •Not conscious,
- •Not cooperative
- •Unstable hemodynamic status,
- •Speaks and understands Turkish,
- •who are under the age of 18,
- •On the 0th or 1st day after surgery,
- •No chest tube,
- •Has sensitivity or trauma in the area (for the study group) where the virtual reality
- •Active COVID-19 infection,
- •Patients with a psychiatric diagnosis
结局指标
主要结局
Pain evaluated using the Visual Analogue Scale
时间窗: Change from before implementation up to 30 minutes
Visual Analogue Scala has been developed to convert some values that cannot be measured numerically into numeric values. The VAS, which is a safe and easily applicable scale tool generally accepted in the world literature, consists of a 10 cm long line and there are subjective descriptive expressions at both ends of the scale (0 cm = none at all and 10 cm = highest degree.)
次要结局
- Diastolic blood pressure(Change from before implementation up to 30 minutes)
- Heart rate(Change from before implementation up to 30 minutes)
- Systolic blood pressure(Change from before implementation up to 30 minutes)
- Respiratory rate(Change from before implementation up to 30 minutes)
- Peripheral oxygen saturation(Change from before implementation up to 30 minutes)
研究者
Tugba CAM YANIK
Principal Investigator in the study/ Research Assistant at Surgical Nursing
Mersin University