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临床试验/NCT01551953
NCT01551953已完成2 期

BEAM COPD: Breathing, Education, Awareness and Movement in Chronic Obstructive Pulmonary Disease

Beth Israel Deaconess Medical Center4 个研究点 分布在 1 个国家目标入组 124 人开始时间: 2011年2月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
124
试验地点
4
主要终点
Feasibility of tai chi intervention

研究概览

简要总结

The main purpose of this study is to determine feasibility and effects of tai chi and mind-body breathing in patients with COPD.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Moderate-severe COPD
  • Age ≥ 40 years

排除标准

  • Subjects with respiratory failure or GOLD stage 4 who are unable to safely perform a 6 minute walk test or otherwise safely exercise as deemed by a physician.
  • COPD exacerbation requiring steroids, antibiotics, ED visit or hospitalization within the past 2 weeks unless physician deems subject at baseline
  • Planned major pulmonary intervention within the next 3 months
  • Hypoxemia on walk test or cardiopulmonary exercise test
  • Inability to ambulate due to vascular or other neuromuscular conditions that would preclude a walk test
  • Clinical signs of unstable cardiovascular disease
  • Severe cognitive dysfunction
  • Non-English speaking
  • Current active participation in pulmonary rehabilitation program or current regular practice of tai chi
  • Physician diagnosis of unstable/untreated clinical depression
  • History of lung cancer

结局指标

主要结局

Feasibility of tai chi intervention

时间窗: 12 weeks

Willingness to participate, adherence, and safety

次要结局

  • Change from baseline- Exercise capacity(baseline, 12 weeks, 24 weeks)
  • Change from baseline- Dyspnea(baseline, 12 weeks, 24 weeks)
  • Change from baseline- Psychosocial well-being(baseline, 12 weeks, 24 weeks)
  • Change from baseline- Physical strength and flexibility(baseline, 12 weeks, 24 weeks)
  • Change from baseline- Disease specific quality of life(baseline, 12 weeks, 24 weeks)
  • Change from baseline- Pulmonary function(baseline, 12 weeks, 24 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Gloria Y. Yeh

Associate Professor of Medicine

Beth Israel Deaconess Medical Center

研究点 (4)

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