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Benefits and challenges of using the cohort multiple randomised controlled trial design for testing an intervention for depression

机译:使用队列的多个随机对照试验设计来测试抑郁症干预措施的益处和挑战

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Background Trials which test the effectiveness of interventions compared with the status quo frequently encounter challenges. The cohort multiple randomised controlled trial (cmRCT) design is an innovative approach to the design and conduct of pragmatic trials which seeks to address some of these challenges. Main text In this article, we report our experiences with the first completed randomised controlled trial (RCT) using the cmRCT design. This trial—the Depression in South Yorkshire (DEPSY) trial—involved comparison of treatment as usual (TAU) with TAU plus the offer of an intervention for people with self-reported long-term moderate to severe depression. In the trial, we used an existing large population-based cohort: the Yorkshire Health Study. We discuss our experiences with recruitment, attrition, crossover, data analysis, generalisability of results, and cost. The main challenges in using the cmRCT design were the high crossover to the control group and the lower questionnaire response rate among patients who refused the offer of treatment. However, the design did help facilitate efficient and complete recruitment of the trial population as well as analysable data that were generalisable to the population of interest. Attrition rates were also smaller than those reported in other depression trials. Conclusion This first completed full trial using the cmRCT design testing an intervention for self-reported depression was associated with a number of important benefits. Further research is required to compare the acceptability and cost effectiveness of standard pragmatic RCT design with the cmRCT design. Trial registration ISRCTN registry: ISRCTN02484593 . Registered on 7 Jan 2013.
机译:与现状相比,测试干预措施有效性的背景试验经常遇到挑战。队列多重随机对照试验(cmRCT)设计是一种创新的方法,用于设计和进行务实试验,旨在解决其中一些挑战。正文在本文中,我们将报告使用cmRCT设计的第一个完整的随机对照试验(RCT)的经验。该试验(南约克郡抑郁症(DEPSY)试验)涉及将常规治疗(TAU)与TAU进行比较,并为自我报告的长期中度至重度抑郁症患者提供了干预措施。在试验中,我们使用了一个现有的基于人口的大型队列:约克郡健康研究。我们讨论了在招聘,减员,交叉,数据分析,结果的可推广性和成本方面的经验。使用cmRCT设计的主要挑战是与对照组的较高交叉和拒绝提供治疗的患者中较低的问卷答复率。但是,该设计确实有助于促进有效且完整地招募试验人群以及可推广到感兴趣人群的可分析数据。减员率也比其他抑郁症试验中报道的小。结论这项首次使用cmRCT设计完成的完整试验测试了一项针对自我报告的抑郁症的干预措施,具有许多重要的益处。需要进一步研究以比较标准实用RCT设计与cmRCT设计的可接受性和成本效益。试用注册ISRCTN注册中心:ISRCTN02484593。 2013年1月7日注册。

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