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Exploring Data Quality Management within Clinical Trials

机译:在临床试验中探索数据质量管理

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摘要

>Background  Clinical trials are an important research method for improving medical knowledge and patient care. Multiple international and national guidelines stipulate the need for data quality and assurance. Many strategies and interventions are developed to reduce error in trials, including standard operating procedures, personnel training, data monitoring, and design of case report forms. However, guidelines are nonspecific in the nature and extent of necessary methods. >Objective  This article gathers information about current data quality tools and procedures used within Australian clinical trial sites, with the aim to develop standard data quality monitoring procedures to ensure data integrity. >Methods  Relevant information about data quality management methods and procedures, error levels, data monitoring, staff training, and development were collected. Staff members from 142 clinical trials listed on the National Health and Medical Research Council (NHMRC) clinical trials Web site were invited to complete a short self-reported semiquantitative anonymous online survey. >Results  Twenty (14%) clinical trials completed the survey. Results from the survey indicate that procedures to ensure data quality varies among clinical trial sites. Centralized monitoring (65%) was the most common procedure to ensure high-quality data. Ten (50%) trials reported having a data management plan in place and two sites utilized an error acceptance level to minimize discrepancy, set at <5% and 5 to 10%, respectively. The quantity of data variables checked (10–100%), the frequency of visits (once-a-month to annually), and types of variables (100%, critical data or critical and noncritical data audits) for data monitoring varied among respondents. The average time spent on staff training per person was 11.58 hours over a 12-month period and the type of training was diverse. >Conclusion  Clinical trial sites are implementing ad hoc methods pragmatically to ensure data quality. Findings highlight the necessity for further research into “standard practice” focusing on developing and implementing publicly available data quality monitoring procedures.
机译:>背景临床试验是提高医学知识和患者护理水平的重要研究方法。多个国际和国家准则规定了数据质量和保证的必要性。为了减少试验中的错误,已开发了许多策略和干预措施,包括标准操作程序,人员培训,数据监视和病例报告表设计。但是,指南在必要方法的性质和范围方面并不明确。 >目标本文收集了有关澳大利亚临床试验站点中当前使用的数据质量工具和程序的信息,目的是开发标准的数据质量监视程序以确保数据完整性。 >方法收集了有关数据质量管理方法和程序,错误级别,数据监视,人员培训和开发的相关信息。来自国家健康与医学研究委员会(NHMRC)临床试验网站上的142条临床试验的工作人员应邀完成了一份简短的自我报告的半定量匿名在线调查。 >结果二十项(14%)临床试验完成了调查。调查结果表明,确保数据质量的程序在临床试验站点之间有所不同。集中监控(65%)是确保高质量数据的最常用程序。十个(50%)试验报告说已经制定了数据管理计划,并且两个站点利用错误接受水平来最大程度地减少差异,分别设置为<5%和5至10%。检查数据变量的数量(10–100%),访问频率(每月一次至每年一次)以及用于数据监视的变量类型(100%,关键数据或关键和非关键数据审核)在受访者中有所不同。在过去的12个月中,每人平均花费在员工培训上的时间为11.58小时,培训类型多种多样。 >结论临床试验站点正在务实地实施临时方法以确保数据质量。调查结果突显了进一步研究“标准做法”的必要性,重点是制定和实施可公开获得的数据质量监控程序。

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