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Prediction of clinical trial enrollment rates
Clinical trials represent a critical milestone of translational and clinical sciences. However, poor recruitment to clinical trials has been a long standing problem affecting institutions all over the world. One way to reduce the cost incurred by insufficient enrollment is to minimize initiating tri...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870517/ https://www.ncbi.nlm.nih.gov/pubmed/35202402 http://dx.doi.org/10.1371/journal.pone.0263193 |
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author | Bieganek, Cameron Aliferis, Constantin Ma, Sisi |
author_facet | Bieganek, Cameron Aliferis, Constantin Ma, Sisi |
author_sort | Bieganek, Cameron |
collection | PubMed |
description | Clinical trials represent a critical milestone of translational and clinical sciences. However, poor recruitment to clinical trials has been a long standing problem affecting institutions all over the world. One way to reduce the cost incurred by insufficient enrollment is to minimize initiating trials that are most likely to fall short of their enrollment goal. Hence, the ability to predict which proposed trials will meet enrollment goals prior to the start of the trial is highly beneficial. In the current study, we leveraged a data set extracted from ClinicalTrials.gov that consists of 46,724 U.S. based clinical trials from 1990 to 2020. We constructed 4,636 candidate predictors based on data collected by ClinicalTrials.gov and external sources for enrollment rate prediction using various state-of-the-art machine learning methods. Taking advantage of a nested time series cross-validation design, our models resulted in good predictive performance that is generalizable to future data and stable over time. Moreover, information content analysis revealed the study design related features to be the most informative feature type regarding enrollment. Compared to the performance of models built with all features, the performance of models built with study design related features is only marginally worse (AUC = 0.78 ± 0.03 vs. AUC = 0.76 ± 0.02). The results presented can form the basis for data-driven decision support systems to assess whether proposed clinical trials would likely meet their enrollment goal. |
format | Online Article Text |
id | pubmed-8870517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-88705172022-02-25 Prediction of clinical trial enrollment rates Bieganek, Cameron Aliferis, Constantin Ma, Sisi PLoS One Research Article Clinical trials represent a critical milestone of translational and clinical sciences. However, poor recruitment to clinical trials has been a long standing problem affecting institutions all over the world. One way to reduce the cost incurred by insufficient enrollment is to minimize initiating trials that are most likely to fall short of their enrollment goal. Hence, the ability to predict which proposed trials will meet enrollment goals prior to the start of the trial is highly beneficial. In the current study, we leveraged a data set extracted from ClinicalTrials.gov that consists of 46,724 U.S. based clinical trials from 1990 to 2020. We constructed 4,636 candidate predictors based on data collected by ClinicalTrials.gov and external sources for enrollment rate prediction using various state-of-the-art machine learning methods. Taking advantage of a nested time series cross-validation design, our models resulted in good predictive performance that is generalizable to future data and stable over time. Moreover, information content analysis revealed the study design related features to be the most informative feature type regarding enrollment. Compared to the performance of models built with all features, the performance of models built with study design related features is only marginally worse (AUC = 0.78 ± 0.03 vs. AUC = 0.76 ± 0.02). The results presented can form the basis for data-driven decision support systems to assess whether proposed clinical trials would likely meet their enrollment goal. Public Library of Science 2022-02-24 /pmc/articles/PMC8870517/ /pubmed/35202402 http://dx.doi.org/10.1371/journal.pone.0263193 Text en © 2022 Bieganek et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Bieganek, Cameron Aliferis, Constantin Ma, Sisi Prediction of clinical trial enrollment rates |
title | Prediction of clinical trial enrollment rates |
title_full | Prediction of clinical trial enrollment rates |
title_fullStr | Prediction of clinical trial enrollment rates |
title_full_unstemmed | Prediction of clinical trial enrollment rates |
title_short | Prediction of clinical trial enrollment rates |
title_sort | prediction of clinical trial enrollment rates |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870517/ https://www.ncbi.nlm.nih.gov/pubmed/35202402 http://dx.doi.org/10.1371/journal.pone.0263193 |
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