Abstract

Adherence to the Consolidated Standards of Reporting Trials (CONSORT) for randomized clinical trials is associated with improvingquality because inadequate reporting in randomized clinical trials may complicate the interpretation and the application of findings to clinical care. To evaluate an automated reporting checklist generation tool that uses natural language processing (NLP), called CONSORT-NLP. This study used published journal articles as training, testing, and validation sets to develop, refine, and evaluate the CONSORT-NLP tool. Articles reporting randomized clinical trials were selected from 25 high-impact-factor journals under the following categories: (1) general and internal medicine, (2) oncology, and (3) cardiac and cardiovascular systems. For an evaluation of the performance of this tool, an accuracy metric defined as the number of correct assessments divided by all assessments was calculated. The CONSORT-NLP tool uses the widely used Portable Document Format as an input file. Of the 37 CONSORT reporting items, 34 (92%) were included in the tool. Of these 34 reporting items, 30 were fully implemented; 28 (93%) of the fully implemented CONSORT reporting items had an accuracy of more than 90% for the validation set. The remaining 2 (7%) had an accuracy between 80% and 90% for the validation set. Two to 5 articles were selected from each of these journals for a total of 158 articles to establish a training set of 111 articles to train CONSORT-NLP for CONSORT reporting items, a testing set of 25 articles to refine CONSORT-NLP, and a validation set of 22 articles to assess the performance of CONSORT-NLP. The CONSORT-NLP tool used the Portable Document Format of the articles as input files. A CONSORT-NLP graphical user interface was built using Java in 2019. The time required to complete the CONSORT checklist manually vs using the CONSORT-NLP tool was compared for 30 articles. Two case studies for randomized clinical trials are provided as an illustration for the CONSORT-NLP tool. For the 30 articles investigated, CONSORT-NLP required a mean (SD) 23.0 (4.1) seconds, whereas the manual reviewer required a mean (SD) 11.9 (2.2), 22.6 (4.6), and 57.6 (7.1) minutes, for 3 reviewers, respectively. The CONSORT-NLP tool is designed to assist in the reporting of randomized clinical trials. Potential users of CONSORT-NLP include clinicians, researchers, and scientists who plan to publish a randomized trial study in a peer-reviewed journal. The use of CONSORT-NLP may help them save substantial time when generating the CONSORT checklist. This tool may also be useful for manuscript reviewers and journal editors who review these articles.

Highlights

  • Inadequate reporting of randomized clinical trials (RCTs) may complicate the interpretation of study results and thereby negatively impact future research or even the application of study results to clinical care

  • Two to 5 articles were selected from each of these journals for a total of 158 articles to establish a training set of 111 articles to train Consolidated Standards of Reporting Trials (CONSORT)-natural language processing (NLP) for CONSORT reporting items, a testing set of 25 articles to refine CONSORT-NLP, and a validation set of 22 articles to assess the performance of CONSORT-NLP

  • Two case studies for randomized clinical trials are provided as an illustration for the CONSORT-NLP tool

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Summary

Introduction

Inadequate reporting of randomized clinical trials (RCTs) may complicate the interpretation of study results and thereby negatively impact future research or even the application of study results to clinical care. Proper reporting may improve the likelihood that published results are reproducible and may contribute to the transparency and structured thinking necessary for high-quality research. Enhancing and harmonizing reporting in publications may advance research and may improve patient outcomes.[1] The well-known reporting guideline for RCTs is called the Consolidated Standards of Reporting Trials (CONSORT), and it has been a fundamental element of quality considerations in clinical trial reporting. A recent literature search with the key words “randomized” AND “controlled” AND “trial” on PubMed yielded more than 40 000 articles in 2017. With these many articles, the issue regarding adherence can be significant. Tremendous effort and resources are required to check these reporting items manually

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