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The effects of pulmonary rehabilitation in patients with non-cystic fibrosis bronchiectasis: protocol for a randomised controlled trial

机译:肺部恢复在非囊性纤维化支气管扩张患者中的影响:随机对照试验的议定书

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Background Non-cystic fibrosis bronchiectasis is characterised by sputum production, exercise limitation and recurrent infections. Although pulmonary rehabilitation is advocated for this patient group, its effects are unclear. The aims of this study are to determine the short and long term effects of pulmonary rehabilitation on exercise capacity, cough, quality of life and the incidence of acute pulmonary exacerbations. Methods/Design This randomised controlled trial aims to recruit 64 patients with bronchiectasis from three tertiary institutions. Participants will be randomly allocated to the intervention group (supervised, twice weekly exercise training with regular review of airway clearance therapy) or a control group (twice weekly telephone support). Measurements will be taken at baseline, immediately following the intervention and at six and 12 months following the intervention period by a blinded assessor. Exercise capacity will be measured using the incremental shuttle walk test and the six-minute walk test. Quality of life and health status will be measured using the Chronic Respiratory Questionnaire, Leicester Cough Questionnaire, Assessment of Quality of Life Questionnaire and the Hospital Anxiety and Depression Scale. The rate of hospitalisation will be captured as well as the incidence of acute pulmonary exacerbations using a daily symptom diary. Discussion Results from this study will help to determine the efficacy of supervised twice-weekly pulmonary rehabilitation upon exercise capacity and quality of life in patients with bronchiectasis and will contribute to clinical practice guidelines for physiotherapists in the management of this population. Trial registration This study protocol is registered with ClinicalTrials.gov (NCT00885521).
机译:背景技术非囊性纤维化支气管扩张的特征在于痰产生,锻炼限制和反复感染。虽然对该患者组提倡肺部康复,但其影响尚不清楚。本研究的目的是确定肺康复对运动能力,咳嗽,生活质量和急性肺癌发病率的短期和长期影响。方法/设计该随机对照试验旨在从三个第三级机构招募64例支气管扩张患者。参与者将随机分配给干预组(通过定期审查气道清关治疗的每周一次运动培训)或对照组(每周两次电话支持)。测量将在基线服用,紧接着由不知情的评估员干预期的干预,并在6至12个月后。使用增量穿梭步行测试和六分钟步行测试将测量运动能力。利用慢性呼吸问卷,莱斯特咳嗽问卷,评估生活质量问卷和医院焦虑和抑郁症的生活质量和健康状况。使用日常症状日记将捕获住院率以及急性肺癌的发病率。本研究的讨论结果将有助于确定受支气管扩张患者的运动能力和生活质量的监督两次肺部恢复的疗效,并将有助于物理治疗师的临床实践指南。试用注册本研究协议在ClinicalTrials.gov(NCT00885521)中注册。

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