Clinical Trial Risk Tool: software application using natural language processing to identify the risk of trial uninformativeness

Thomas A Wood, D. McNair
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引用次数: 0

Abstract

Background: A large proportion of clinical trials end without delivering results that are useful for clinical, policy, or research decisions. This problem is called “uninformativeness”. Some high-risk indicators of uninformativeness can be identified at the stage of drafting the protocol, however the necessary information can be hard to find in unstructured text documents. Methods: We have developed a browser-based tool which uses natural language processing to identify and quantify the risk of uninformativeness. The tool reads and parses the text of trial protocols and identifies key features of the trial design, which are fed into a risk model. The application runs in a browser and features a graphical user interface that allows a user to drag and drop the PDF of the trial protocol and visualize the risk indicators and their locations in the text. The user can correct inaccuracies in the tool’s parsing of the text. The tool outputs a PDF report listing the key features extracted. The tool is focused HIV and tuberculosis trials but could be extended to more pathologies in future. Results: On a manually tagged dataset of 300 protocols, the tool was able to identify the condition of a trial with 100% area under curve (AUC), presence or absence of statistical analysis plan with 87% AUC, presence or absence of effect estimate with 95% AUC, number of subjects with 69% accuracy, and simulation with 98% AUC. On a dataset of 11,925 protocols downloaded from ClinicalTrials.gov, the tool was able to identify trial phase with 75% accuracy, number of arms with 58% accuracy, and the countries of investigation with 87% AUC. Conclusion: We have developed and validated a natural language processing tool for identifying and quantifying risks of uninformativeness in clinical trial protocols. The software is open-source and can be accessed at the following link: https://app.clinicaltrialrisk.org
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临床试验风险工具:使用自然语言处理识别试验不信息风险的软件应用程序
背景:很大比例的临床试验没有提供对临床、政策或研究决策有用的结果。这个问题被称为“信息不充分”。在起草议定书的阶段可以确定一些信息不充分的高风险指标,但是在非结构化文本文件中很难找到必要的信息。方法:我们开发了一个基于浏览器的工具,使用自然语言处理来识别和量化信息缺失的风险。该工具读取和解析试验协议的文本,识别试验设计的关键特征,并将其输入风险模型。该应用程序在浏览器中运行,具有图形用户界面,允许用户拖放试验方案的PDF,并将风险指标及其在文本中的位置可视化。用户可以在工具解析文本时纠正不准确的地方。该工具输出一个PDF报告,其中列出了提取的关键特性。该工具主要用于艾滋病毒和结核病的试验,但将来可能会扩展到更多的疾病。结果:在300个方案的手动标记数据集上,该工具能够识别出曲线下面积(AUC)为100%的试验条件,统计分析计划的存在与否为87%的AUC,效应估计的存在与否为95%的AUC,受试者数量的准确率为69%,模拟的AUC为98%。在从ClinicalTrials.gov下载的11,925个方案的数据集上,该工具能够以75%的准确率识别试验阶段,58%的准确率识别治疗组数量,87%的AUC识别调查国家。结论:我们已经开发并验证了一种自然语言处理工具,用于识别和量化临床试验方案中信息不全的风险。该软件为开源软件,可通过以下链接访问:https://app.clinicaltrialrisk.org
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Gates Open Research
Gates Open Research Immunology and Microbiology-Immunology and Microbiology (miscellaneous)
CiteScore
3.60
自引率
0.00%
发文量
90
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