The Effect of Virtual Reality on Vital Signs and Anxiety in Myocardial Infarction Patients Admitted to Cardiology Intensive Care Unit: A Randomized Controlled Study.
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Anxiety Level
研究概览
简要总结
This study was designed to investigate the effects of VR (virtual reality) glasses on vital signs and anxiety in conscious patients diagnosed with myocardial infarction and admitted to the cardiology intensive care unit.
详细描述
This study was designed to investigate the effects of VR (virtual reality) glasses on vital signs and anxiety in conscious patients with myocardial infarction (MI) admitted to the cardiology intensive care unit. Studies examining the psychological (anxiety) and physiological (vital signs) effects of VR application on MI patients in cardiology intensive care units are quite limited. In this context, this study aims to examine the effects of VR glasses application on the vital signs (blood pressure, heart rate, SPO2, respiratory rate) and anxiety levels of MI patients in intensive care, within the framework of a randomized experimental design. The data obtained are expected to make significant contributions to the integration of technological interventions into cardiovascular disease management.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Health Services Research
- 盲法
- Single (Outcomes Assessor)
盲法说明
Outcomes Assessor does not know whether patients are in the experimental group or the control group.
入排标准
- 年龄范围
- 18 Years 至 70 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •The patient is in intensive care.
- •The patient has been diagnosed with myocardial infarction.
- •The patient is between 18 and 70 years old.
- •The patient is conscious.
- •The patient is oriented and cooperative.
- •The patient volunteers to participate in the study.
- •The patient is open to communication.
- •The patient agrees to participate in the study.
- •The patient has no mental, visual, auditory, or speech impairment.
- •The patient has undergone stent placement.
- •The patient has STEMI.
排除标准
- •The patient has a psychiatric disorder.
- •The patient has any communication impairment.
研究组 & 干预措施
CONTROL GROUP
In this group, vital signs and anxiety levels will be measured as pre-test and post-test without any intervention.
EXPERIMENTAL GROUP
Participants will be shown a video with nature images through virtual reality glasses, and their vital signs and anxiety levels will be measured.
干预措施: virtual reality glasses (Other)
结局指标
主要结局
Anxiety Level
时间窗: Periprocedural
The patient's anxiety level will be measured using the State Anxiety Scale (STAI Form TX-1).
Vital Signs - Blood pressure measurements (SBP, DBP)
时间窗: Periprocedural
Blood pressure measurements (SBP, DBP)
Vital Signs- heart rate
时间窗: Periprocedural
heart rate will be taken.
Vital Signs - respiratory rate per minute
时间窗: Periprocedural
respiratory rate per minute will be taken.
次要结局
未报告次要终点
研究者
Yavuz Uren
Principal İnvestigatorI(Dr.)
Yuzuncu Yil University