Study design for a randomised controlled trial to explore the modality and mechanism of Tai Chi in the pulmonary rehabilitation of chronic obstructive pulmonary disease

被引:10
|
作者
Fu, Juan-Juan [1 ]
Min, Jie [1 ]
Yu, Peng-Ming [2 ]
McDonald, Vanessa M. [3 ,4 ]
Mao, Bing [1 ]
机构
[1] Sichuan Univ, Resp Grp, Dept Integrated Tradit Chinese & Western Med, West China Hosp, Chengdu, Peoples R China
[2] Sichuan Univ, West China Hosp, Dept Rehabil, Chengdu, Peoples R China
[3] Univ Newcastle, Prior Res Ctr Asthma & Resp Dis, Newcastle, NSW, Australia
[4] Univ Newcastle, Fac Hlth, Sch Nursing & Midwifery, Newcastle, NSW, Australia
来源
BMJ OPEN | 2016年 / 6卷 / 08期
关键词
QUALITY-OF-LIFE; RESPIRATORY SOCIETY STATEMENT; SYSTEMIC INFLAMMATION; LUNG-FUNCTION; EXERCISE; HEALTH; ASTHMA; EXACERBATION; COPD; OUTCOMES;
D O I
10.1136/bmjopen-2016-011297
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction:Although pulmonary rehabilitation (PR) is associated with significant clinical benefits in chronic obstructive pulmonary disease (COPD) and has been recommended by guidelines, PR with conventional exercise training has not been widely applied in the clinic because of its inherent limitations. Alternative exercise such as Tai Chi has been investigated and the results are promising. However, the strengths and weaknesses of the exercise modality of Tai Chi, conventional PR and a combination of Tai Chi and conventional PR and the possible mechanisms underlying Tai Chi exercise remain unclear. This study aims to address the above research gaps in a well-designed clinical trial. Methods and analysis:This study is a single-blind, randomised controlled trial. Participants with stable COPD will be recruited and randomly assigned to one of four groups receiving Tai Chi exercise, conventional PR using a total body recumbent stepper (TBRS), combined Tai Chi and TBRS, or usual care (control) in a 1:1:1:1 ratio. Participants will perform 30 min of supervised exercise three times a week for 8 weeks; they will receive sequential follow-ups until 12 months after recruitment. The primary outcome will be health-related quality of life as measured by the St George's Respiratory Questionnaire. Secondary outcomes will include 6 min walking distance, pulmonary function, the modified Medical Research Council Dyspnoea Scale, the COPD Assessment Test, the Hospital Anxiety and Depression Scale, the Berg Balance Scale, exacerbation frequency during the study period, and systemic inflammatory and immune markers. Ethics and dissemination:Ethics approval has been granted by the Clinical Trial and Biomedical Ethics Committee of West China Hospital of Sichuan University (No TCM-2015-82). Written informed consent will be obtained from each participant before any procedures are performed. The study findings will be published in peer-reviewed journals and presented at national and international conferences.
引用
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页数:11
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