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临床试验/NCT00485043
NCT00485043已完成1 期

Effects of Modified T'ai Chi Exercise on Physical Function, Pain, and Stiffness in Older Adults With Lower Extremity Osteoarthritis

University of Kansas0 个研究点目标入组 30 人开始时间: 2006年1月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
30
主要终点
physical function

研究概览

简要总结

The purpose of this study was to evaluate the effects of TC for Arthritis on physical function, pain, and stiffness in older adults with knee/hip OA. Two hypotheses were tested:

  1. Individuals in the TC group will demonstrate greater improvements in physical function compared to control group participants.
  2. Individuals in the TC group will demonstrate greater decreases in pain and stiffness compared to control group participants.

详细描述

Exercise is considered a vital component of osteoarthritis (OA) treatment. T'ai Chi (TC) is a unique exercise intervention with low-velocity movements. Few studies have addressed the effects of TC on arthritis symptoms and function. TC for Arthritis was modified specifically for people with OA and consists of a standardized set of forms.

The purpose of this study was to evaluate the effectiveness of a low-dose TC for Arthritis on physical function, pain, and stiffness in individuals with OA.

Twenty-seven older adults with OA (mean age-81.3 years) completed an 8 week non-randomized controlled pre-post test quasi-experimental design study of TC for Arthritis. Physical function, pain, and stiffness were measured at baseline and 8 weeks for the TC and control groups using the WOMAC™ 3.1 Index. Qualitative data from interviews and participant observations were analyzed in order to understand the participants' expectations and experiences with TC.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
60 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Ability to walk independently,
  • Speak and understand English,
  • Understand the consent process; and
  • Give informed consent.

排除标准

  • Participation in rehabilitation or another TC class,
  • At the time of recruitment; and
  • Inability to confirm medical stability for safe participation with healthcare provider.

结局指标

主要结局

physical function

时间窗: 8 weeks

次要结局

  • pain and stiffness(8 weeks)

研究者

申办方类型
Other

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