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穴位按摩对疲劳的影响

2026年9月29日 更新者:Esra Cavusoglu、Mersin University

穴位按摩对护生疲劳的影响:一项随机对照研究

In this study, it is aimed to determine the effect of acupressure on fatigue in nursing students.

研究概览

详细说明

In this study, 68 nursing students were randomly assigned to the acupressure and placebo (sham) acupressure groups. In the acupressure group (n=34), compression was applied to the 7th point of the heart meridian (HT7), the 4th point of the large intestine meridian (LI4), the 36th point of the stomach meridian (ST36), and the 6th point of the spleen meridian (SP6). Depending on the preparation and compression time at each point, the session duration of each student lasted an average of 20 minutes. In the sham group (n=34), pressure was applied approximately 1-1.5 cm away from the HT7, LI4, ST36, SP6 points. In the sham group, the acupressure application time lasted for an average of 20 minutes. At the end of the application, after the data collection process was completed, the sham group was taught the correct acupuncture points. Students applied acupressure three times a week for a total of 12 sessions for four weeks. Data were collected before and four weeks after the application in the acupressure and sham acupressure groups.

研究类型

介入性

注册 (实际的)

68

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Yenişehir
      • Mersin、Yenişehir、土耳其(türkiye)
        • Mersin University Faculty of Nursing
      • Mersin、Yenişehir、土耳其(türkiye)、33343
        • Mersin Üniversitesi

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子
  • 成人
  • 年长者

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Students studying at Mersin University Faculty of Nursing as 4th grade during the data collection date,
  • Those who agree to participate in the study,
  • No deformity or lesions in the areas where acupressure will be applied
  • No acupressure experience
  • No sleep disorder diagnosis and no medical treatment
  • No diagnosis of anxiety disorder and no medical treatment No diagnosis of depression and no medical treatment
  • Coffee, cigarette and alcohol-free,
  • No mental illness,
  • Able to understand and speak Turkish and
  • Those who signed the Informed Consent Form will be included in the study.

Exclusion Criteria:

  • Students studying at Mersin University Faculty of Nursing outside the 4th grade during the data collection date,
  • Those who do not agree to participate in the study,
  • Those who have any deformity or lesion in the areas where acupressure will be applied
  • Experienced with acupressure
  • Diagnosed with sleep disorder and receiving medical treatment
  • Diagnosed with anxiety disorder and receiving medical treatment
  • Diagnosed with depression and receiving medical treatment
  • Coffee, cigarette and alcohol addiction,
  • Having mental illness,
  • who cannot understand or speak Turkish
  • Those who do not sign the Informed Consent Form will not be included in the study.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:其他
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:Acupressure group

The acupressure (experimental) group will apply acupressure to themselves three times a week for a total of 12 sessions for four weeks.

In the acupressure group, acupressure will be applied to the heart meridian 7th point (HT7), large intestine meridian 4th point (LI4), stomach meridian 36th point (ST36) and spleen meridian 6th point (SP6). After pressing each point for a certain period of time, a total of two minutes of rest periods will be applied by the researcher.

其他名称:
  • 实验组
假比较器:Sham Acupressure Group

The sham acupressure group will apply acupressure to themselves three times a week for a total of 12 sessions for four weeks.

In the sham acupressure group, acupressure will be applied on the bone region where the meridians do not pass, approximately 1-1.5 cm away from the HT7, LI4, ST36, SP6 points. The application process will continue in the same way with acupressure group and the pressure intensity will be less.

其他名称:
  • 深水集团

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Fatigue evaluated using the Fatigue Severity Scale
大体时间:Change from before implementation and 4th week of practice

It is a Likert-type scale consisting of a total of nine items, each item being evaluated between 1 and 7 (1=I totally disagree, 7=I totally agree). The fatigue score is obtained by dividing the total score obtained from the scale by the number of scale items. The score that can be obtained from the scale varies between 9 and 63. A high score indicates an increased level of fatigue.

Change from before implementation and 4th week of practice

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 研究主任:Meral Gün, Doctorate、Mersin University

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2021年9月15日

初级完成 (实际的)

2021年9月15日

研究完成 (实际的)

2021年12月31日

研究注册日期

首次提交

2022年4月5日

首先提交符合 QC 标准的

2022年4月13日

首次发布 (实际的)

2022年4月20日

研究记录更新

最后更新发布 (实际的)

2026年10月2日

上次提交的符合 QC 标准的更新

2026年9月29日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

其他研究编号

  • MersinUu

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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