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临床试验/ChiCTR-IIR-16009056
ChiCTR-IIR-16009056已完成3 期

探討有效改善社區中共病長者疲憊的方法

Association of Hong Kong Nursing Staff1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 1990年1月1日最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
140
试验地点
1
主要终点
fatigue

研究概览

简要总结

探討有效改善社區中共病長者疲憊的方法

研究设计

研究类型
干预性研究
主要目的
随机平行对照
盲法
Single

入排标准

年龄范围
60 至 —(—)
性别
All

入选标准

  • aged 60 or above;
  • able to communicate;
  • Abbreviated Mental Test score equal or greater than 6;
  • score of reduced activity subscale of Multidimensional Fatigue Inventory >=10.

排除标准

  • visually imparied;
  • auditory imparied;
  • inability to walk;
  • have pre-existing psychiatric diagnosis;
  • musculoskeletal contracture;
  • acute exacerbation of osteoarthritis;
  • received cancer treatments in the past 24 months;
  • have advanced or terminal malignancies as being labelled as supportive or terminal care by qualified physicians;
  • received operation in the past 6 months;
  • participate in other structured exercise programme.

研究组 & 干预措施

Two groups

Structured aerobic exercise moderate intensity as determined by Borg scale of Perceived Exertion, 12 weeks, 3 times per week versus health talks 1 hour per each session, total 6 sessions, 12 weeks, once per two weeks

结局指标

主要结局

fatigue

时间窗: pre-intervention, post-intervention, 3 months after intervention

次要结局

  • mood status(pre-intervention, post-intervention, 3 months after intervention)
  • exercise tolerance capacity(pre-intervention, post-intervention, 3 months after intervention)

研究者

研究点 (1)

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