The Effect of Acupressure After Angiography on Pain Level and Hemodynamic Variables Randomized Controlled Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 124
- 试验地点
- 2
- 主要终点
- Pain evaluated using the visual analog scale
研究概览
简要总结
This randomized controlled study evaluates the effect of acupressure application on the pain level patients after angioography. The hypothesis of this study is that acupressure reduces pain levels and stabilizes hemodynamic variables.
详细描述
In the study, 124 patients will randomly assigned to acupressure/experimental group and control group. To the acupressure/experimental group (n = 62), an average of 15 minutes will be applied to the LI4 (liver, between thumb and forefinger), P6 (pericardium, three fingers above the wrist) and LI 11 is located the area where the elbow bend. On the other hand, no other intervention will be applied to the control group other than routine treatment and nursing care. The primary outcome of the research is the effect of acupressure on the pain of patients. The secondary outcome of the study is to determine the effect of acupressure on the hemodynamic variables. The pain and hemodynamic variables will be collected before, immediately after the application, 10th, 20th and 30th minutes after the application. Data will also be collected from the control group at the same time.
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)
盲法说明
Due to the nature of the research, participants and researchers cannot be blinded. Analyzes will be made by a biostatistician independent of the research and the statistician will be blinded.
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
- 是
入选标准
- •Agreeing to participate in the research (signing the Informed Consent Form),
- •Conscious and cooperative,
- •Speaks and understands Turkish,
- •Over 18 years of age,
- •Stable general condition,
- •No sensitivity in the area where acupressure will be applied,
- •No active COVID-19 infection,
- •Patients without any psychiatric diagnosis will be included.
排除标准
- •Do not agreeing to participate in the research (signing the Informed Consent Form),
- •Do not conscious and cooperative,
- •Do not speaks and understands Turkish,
- •Do not over 18 years of age,
- •Do not stable general condition,
- •Having sensitivity in the area where acupressure will be applied,
- •Having active COVID-19 infection,
- •Patients with any psychiatric diagnosis will be included.
结局指标
主要结局
Pain evaluated using the visual analog scale
时间窗: Change from before implementation and immediately after, 10th, 20th and 30th minutes after implementation
The total scale score is in the range of 0 cm (minimum) -10 cm (maximum). A score of 0 indicates no pain and a score of 10 indicates very severe pain.
次要结局
- Heart rate(Change from before implementation and immediately after, 10th, 20th and 30th minutes after implementation)
- Diastolic blood pressure(Change from before implementation and immediately after, 10th, 20th and 30th minutes after implementation)
- Systolic blood pressure(Change from before implementation and immediately after, 10th, 20th and 30th minutes after implementation)
- Respiratory rate(Change from before implementation and immediately after, 10th, 20th and 30th minutes after implementation)
- Peripheral oxygen saturation(Change from before implementation and immediately after, 10th, 20th and 30th minutes after implementation)
研究者
Tugba CAM YANIK
Principal Investigator
Mersin University