针对 COVID-19 护士流行病疲劳和恢复能力的在线正念疗法
2024年5月23日 更新者：Chimei Medical Center
评估在线正念疗法对 COVID-19 隔离病房护士的流行病疲劳和恢复能力的影响
本研究评估了在线正念疗法对 COVID-19 隔离病房护士的大流行性疲劳和恢复能力的影响。
60 名护士被分为实验组和对照组，实验组接受为期 6 周的在线正念课程。
研究概览
详细说明
本研究评估了在线正念疗法在减少大流行性疲劳和增强 COVID-19 隔离病房护士的适应能力方面的有效性。
采用重复测量的准实验设计，将 60 名护士分为实验组和对照组。
实验组参加了为期 6 周的在线正念课程。
在预测试、三周和六周后使用流行病疲劳和复原力问卷来衡量结果。
研究类型
介入性
注册 (实际的)
60
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
-
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其他（非美國）
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Tainan City、其他（非美國）、台湾、71004
- Chi Mei Medical Center
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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
- 成人
- 年长者
接受健康志愿者
不
描述
纳入标准：
- 20多岁了。
- COVID-19 专用病房和专用重症监护病房的护士。
排除标准：
- 出席困难
- 少于在线正念治疗课程总数的 80%
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：非随机化
- 介入模型：并行分配
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的：实验组将接受为期6周的在线正念课程
实验组接受了为期 6 周的在线正念课程，每周一次，每次 90 分钟。
参与者在课程开始前、第 3 周和第 6 周完成了问卷调查。
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实验组接受了为期 6 周的在线正念课程，每周一次，每次 90 分钟。
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无干预：控制组
一般日常护理
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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 |
|---|---|---|
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流行性疲劳
大体时间：6周
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使用封锁/流行病疲劳量表 (LFS) 测量流行病疲劳。
该量表共有 10 个项目，衡量流行病疲劳程度。
该量表的总分范围为10-50。
它表明，流行病疲劳随着量表总分的增加而增加。
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6周
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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弹力
大体时间：6周
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使用康纳戴维森复原力量表 (CD-RISC) 衡量个人复原力。
该量表共有 25 个项目来衡量弹性。
量表总分范围为0-100。
它表明，弹性随着量表总分的增加而增加。
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6周
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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。
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
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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)
2022年10月1日
初级完成 (实际的)
2023年5月31日
研究完成 (实际的)
2023年5月31日
研究注册日期
首次提交
2024年5月23日
首先提交符合 QC 标准的
2024年5月23日
首次发布 (实际的)
2024年5月29日
研究记录更新
最后更新发布 (实际的)
2024年5月29日
上次提交的符合 QC 标准的更新
2024年5月23日
最后验证
2024年5月1日
更多信息
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.