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Opportunities and Challenges for Decentralized Clinical Trials: European Regulators’ Perspective
Decentralized clinical trials (DCTs) have the potential to improve accessibility, diversity, and retention in clinical trials by moving trial activities to participants’ homes and local surroundings. In this study, we conducted semi‐structured interviews with 20 European regulators to identify regul...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540149/ https://www.ncbi.nlm.nih.gov/pubmed/35488483 http://dx.doi.org/10.1002/cpt.2628 |
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author | de Jong, Amos J. van Rijssel, Tessa I. Zuidgeest, Mira G. P. van Thiel, Ghislaine J. M. W. Askin, Scott Fons‐Martínez, Jaime De Smedt, Tim de Boer, Anthonius Santa‐Ana‐Tellez, Yared Gardarsdottir, Helga |
author_facet | de Jong, Amos J. van Rijssel, Tessa I. Zuidgeest, Mira G. P. van Thiel, Ghislaine J. M. W. Askin, Scott Fons‐Martínez, Jaime De Smedt, Tim de Boer, Anthonius Santa‐Ana‐Tellez, Yared Gardarsdottir, Helga |
author_sort | de Jong, Amos J. |
collection | PubMed |
description | Decentralized clinical trials (DCTs) have the potential to improve accessibility, diversity, and retention in clinical trials by moving trial activities to participants’ homes and local surroundings. In this study, we conducted semi‐structured interviews with 20 European regulators to identify regulatory challenges and opportunities for the implementation of DCTs in the European Union. The key opportunities for DCTs that were recognized by regulators include a reduced participation burden, which could facilitate the participation of underserved patients. In addition, regulators indicated that data collected in DCTs are expected to be more representative of the real world. Key challenges recognized by regulators for DCTs include concerns regarding investigator oversight and participants’ safety when physical examinations and face‐to‐face contact are limited. To facilitate future learning, hybrid clinical trials with both on‐site and decentralized elements are proposed by the respondents. |
format | Online Article Text |
id | pubmed-9540149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95401492022-10-14 Opportunities and Challenges for Decentralized Clinical Trials: European Regulators’ Perspective de Jong, Amos J. van Rijssel, Tessa I. Zuidgeest, Mira G. P. van Thiel, Ghislaine J. M. W. Askin, Scott Fons‐Martínez, Jaime De Smedt, Tim de Boer, Anthonius Santa‐Ana‐Tellez, Yared Gardarsdottir, Helga Clin Pharmacol Ther Research Decentralized clinical trials (DCTs) have the potential to improve accessibility, diversity, and retention in clinical trials by moving trial activities to participants’ homes and local surroundings. In this study, we conducted semi‐structured interviews with 20 European regulators to identify regulatory challenges and opportunities for the implementation of DCTs in the European Union. The key opportunities for DCTs that were recognized by regulators include a reduced participation burden, which could facilitate the participation of underserved patients. In addition, regulators indicated that data collected in DCTs are expected to be more representative of the real world. Key challenges recognized by regulators for DCTs include concerns regarding investigator oversight and participants’ safety when physical examinations and face‐to‐face contact are limited. To facilitate future learning, hybrid clinical trials with both on‐site and decentralized elements are proposed by the respondents. John Wiley and Sons Inc. 2022-05-17 2022-08 /pmc/articles/PMC9540149/ /pubmed/35488483 http://dx.doi.org/10.1002/cpt.2628 Text en © 2022 The Authors. Clinical Pharmacology & Therapeutics published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research de Jong, Amos J. van Rijssel, Tessa I. Zuidgeest, Mira G. P. van Thiel, Ghislaine J. M. W. Askin, Scott Fons‐Martínez, Jaime De Smedt, Tim de Boer, Anthonius Santa‐Ana‐Tellez, Yared Gardarsdottir, Helga Opportunities and Challenges for Decentralized Clinical Trials: European Regulators’ Perspective |
title | Opportunities and Challenges for Decentralized Clinical Trials: European Regulators’ Perspective |
title_full | Opportunities and Challenges for Decentralized Clinical Trials: European Regulators’ Perspective |
title_fullStr | Opportunities and Challenges for Decentralized Clinical Trials: European Regulators’ Perspective |
title_full_unstemmed | Opportunities and Challenges for Decentralized Clinical Trials: European Regulators’ Perspective |
title_short | Opportunities and Challenges for Decentralized Clinical Trials: European Regulators’ Perspective |
title_sort | opportunities and challenges for decentralized clinical trials: european regulators’ perspective |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540149/ https://www.ncbi.nlm.nih.gov/pubmed/35488483 http://dx.doi.org/10.1002/cpt.2628 |
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