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首页> 外文期刊>BMJ Open Respiratory Research >Investigating outcome measures for assessing airway clearance techniques in adults with cystic fibrosis: protocol of a single-centre randomised controlled crossover trial
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Investigating outcome measures for assessing airway clearance techniques in adults with cystic fibrosis: protocol of a single-centre randomised controlled crossover trial

机译:调查囊性纤维化成年人气道清关技术的结果措施:单中心随机对照交叉试验的协议

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Introduction Airway clearance techniques (ACTs) are a gold standard of cystic fibrosis management; however, the majority of research evidence for their efficacy is of low standard; often attributed to the lack of sensitivity from outcome measures (OMs) used historically. This randomised controlled trial (RCT) investigates these standard OMs (sputum weight, forced expiratory volume in 1 s) and new OMs (electrical impedance tomography (EIT), multiple breath washout (MBW) and impulse oscillometry (IOS)) to determine the most useful measures of ACT.Methods and analysis This is a single-centre RCT with crossover design. Participants perform MBW, IOS and spirometry, and then are randomised to either rest or supervised ACT lasting 30–60 min. MBW, IOS and spirometry are repeated immediately afterwards. EIT and sputum are collected during rest/ACT. On a separate day, the OMs are performed with the other intervention. Primary endpoint is difference in change in OMs before and after ACT/rest. Sample size was calculated with 80% power and significance of 5% for each OM (target n=64).Ethics and dissemination Ethics approval was gained from the London–Chelsea Research Ethics Committee (reference 16/LO/0995, project ID 154635). Dissemination will involve scientific conference presentation and publication in a peer-reviewed journal.Trial registration numbers ISRCTN11220163 and NCT02721498.
机译:简介气道清关技术(行为)是囊性纤维化管理的金标准;但是,大多数研究证据的功效是低标准的;通常归因于历史上使用的结果措施(OMS)缺乏敏感性。这种随机对照试验(RCT)研究了这些标准OMS(痰重量,强制呼气量,在1S)和新的OMS(电阻断层扫描(EIT),多呼吸冲刷(MBW)和脉冲示波器(IOS))中以确定最多Act.methods和分析的有用措施是一个具有交叉设计的单中心RCT。参与者执行MBW,iOS和Spirometry,然后随机随机化或监督行为持续30-60分钟。之后立即重复MBW,iOS和肺活量测定法。在休息/行动期间收集EIT和痰。在一个单独的一天,OMS是通过其他干预进行的。主要端点是在行为/休息之前和之后OMS变化的差异。对于每个OM的80%功率和显着性计算样品大小(目标n = 64)。伦敦 - 切尔西研究伦理委员会(参考文献16 / LO / 0995,项目ID 154635)获得了50%的5%(目标n = 64)。言语和传播伦理批准。传播将涉及科学会议介绍和出版物在同行评审期刊.Tial注册号ISRCTN11220163和NCT02721498中。

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