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Challenges and Best Practices in Ethical Review of Human and Organizational Factors Studies in Health Technology: a Synthesis of Testimonies: A Joint Contribution from the International Medical Informatics Association's Human Factors Engineering and the European Federation for Medicatl Informatics’ Human and Organizational Factors of Medical Informatics Working Groups
Objective: Human and Organizational Factors (HOF) studies in health technology involve human beings and thus require Institutional Review Board (IRB) approval. Yet HOF studies have specific constraints and methods that may not fit standard regulations and IRB practices. Gaining IRB approval may pose...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Georg Thieme Verlag KG
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7442520/ https://www.ncbi.nlm.nih.gov/pubmed/32303100 http://dx.doi.org/10.1055/s-0040-1701979 |
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author | Peute, Linda W. Lichtner, Valentina Baysari, Melissa T. Hägglund, Maria Homco, Juell Jansen-Kosterink, Stephanie Jauregui, Ignacio Kaipio, Johanna Kuziemsky, Craig E. Lehnbom, Elin Christina Leite, Francisca Lesselroth, Blake Luna, Daniel Otero, Carlos Pedersen, Rune Pelayo, Sylvia Santos, Raquel Silva, Nuno-André Tyllinen, Mari Van Velsen, Lex Zheng, Wu Yi Jaspers, Monique Marcilly, Romaric |
author_facet | Peute, Linda W. Lichtner, Valentina Baysari, Melissa T. Hägglund, Maria Homco, Juell Jansen-Kosterink, Stephanie Jauregui, Ignacio Kaipio, Johanna Kuziemsky, Craig E. Lehnbom, Elin Christina Leite, Francisca Lesselroth, Blake Luna, Daniel Otero, Carlos Pedersen, Rune Pelayo, Sylvia Santos, Raquel Silva, Nuno-André Tyllinen, Mari Van Velsen, Lex Zheng, Wu Yi Jaspers, Monique Marcilly, Romaric |
author_sort | Peute, Linda W. |
collection | PubMed |
description | Objective: Human and Organizational Factors (HOF) studies in health technology involve human beings and thus require Institutional Review Board (IRB) approval. Yet HOF studies have specific constraints and methods that may not fit standard regulations and IRB practices. Gaining IRB approval may pose difficulties for HOF researchers. This paper aims to provide a first overview of HOF study challenges to get IRB review by exploring differences and best practices across different countries. Methods: HOF researchers were contacted by email to provide a testimony about their experience with IRB review and approval. Testimonies were thematically analyzed and synthesized to identify and discuss shared themes. Results: Researchers from seven European countries, Argentina, Canada, Australia, and the United States answered the call. Four themes emerged that indicate shared challenges in legislation, IRB inefficiencies and inconsistencies, general regulation and costs, and lack of HOF study knowledge by IRB members. We propose a model for IRB review of HOF studies based on best practices. Conclusion: International criteria are needed that define low and high-risk HOF studies, to allow identification of studies that can undergo an expedited (or exempted) process from those that need full IRB review. Enhancing IRB processes in such a way would be beneficial to the conduct of HOF studies. Greater knowledge and promotion of HOF methods and evidence-based HOF study designs may support the evolving discipline. Based on these insights, training and guidance to IRB members may be developed to support them in ensuring that appropriate ethical issues for HOF studies are considered. |
format | Online Article Text |
id | pubmed-7442520 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Georg Thieme Verlag KG |
record_format | MEDLINE/PubMed |
spelling | pubmed-74425202020-08-24 Challenges and Best Practices in Ethical Review of Human and Organizational Factors Studies in Health Technology: a Synthesis of Testimonies: A Joint Contribution from the International Medical Informatics Association's Human Factors Engineering and the European Federation for Medicatl Informatics’ Human and Organizational Factors of Medical Informatics Working Groups Peute, Linda W. Lichtner, Valentina Baysari, Melissa T. Hägglund, Maria Homco, Juell Jansen-Kosterink, Stephanie Jauregui, Ignacio Kaipio, Johanna Kuziemsky, Craig E. Lehnbom, Elin Christina Leite, Francisca Lesselroth, Blake Luna, Daniel Otero, Carlos Pedersen, Rune Pelayo, Sylvia Santos, Raquel Silva, Nuno-André Tyllinen, Mari Van Velsen, Lex Zheng, Wu Yi Jaspers, Monique Marcilly, Romaric Yearb Med Inform Objective: Human and Organizational Factors (HOF) studies in health technology involve human beings and thus require Institutional Review Board (IRB) approval. Yet HOF studies have specific constraints and methods that may not fit standard regulations and IRB practices. Gaining IRB approval may pose difficulties for HOF researchers. This paper aims to provide a first overview of HOF study challenges to get IRB review by exploring differences and best practices across different countries. Methods: HOF researchers were contacted by email to provide a testimony about their experience with IRB review and approval. Testimonies were thematically analyzed and synthesized to identify and discuss shared themes. Results: Researchers from seven European countries, Argentina, Canada, Australia, and the United States answered the call. Four themes emerged that indicate shared challenges in legislation, IRB inefficiencies and inconsistencies, general regulation and costs, and lack of HOF study knowledge by IRB members. We propose a model for IRB review of HOF studies based on best practices. Conclusion: International criteria are needed that define low and high-risk HOF studies, to allow identification of studies that can undergo an expedited (or exempted) process from those that need full IRB review. Enhancing IRB processes in such a way would be beneficial to the conduct of HOF studies. Greater knowledge and promotion of HOF methods and evidence-based HOF study designs may support the evolving discipline. Based on these insights, training and guidance to IRB members may be developed to support them in ensuring that appropriate ethical issues for HOF studies are considered. Georg Thieme Verlag KG 2020-08 2020-04-17 /pmc/articles/PMC7442520/ /pubmed/32303100 http://dx.doi.org/10.1055/s-0040-1701979 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited. |
spellingShingle | Peute, Linda W. Lichtner, Valentina Baysari, Melissa T. Hägglund, Maria Homco, Juell Jansen-Kosterink, Stephanie Jauregui, Ignacio Kaipio, Johanna Kuziemsky, Craig E. Lehnbom, Elin Christina Leite, Francisca Lesselroth, Blake Luna, Daniel Otero, Carlos Pedersen, Rune Pelayo, Sylvia Santos, Raquel Silva, Nuno-André Tyllinen, Mari Van Velsen, Lex Zheng, Wu Yi Jaspers, Monique Marcilly, Romaric Challenges and Best Practices in Ethical Review of Human and Organizational Factors Studies in Health Technology: a Synthesis of Testimonies: A Joint Contribution from the International Medical Informatics Association's Human Factors Engineering and the European Federation for Medicatl Informatics’ Human and Organizational Factors of Medical Informatics Working Groups |
title | Challenges and Best Practices in Ethical Review of Human and Organizational Factors Studies in Health Technology: a Synthesis of Testimonies: A Joint Contribution from the International Medical Informatics Association's Human Factors Engineering and the European Federation for Medicatl Informatics’ Human and Organizational Factors of Medical Informatics Working Groups |
title_full | Challenges and Best Practices in Ethical Review of Human and Organizational Factors Studies in Health Technology: a Synthesis of Testimonies: A Joint Contribution from the International Medical Informatics Association's Human Factors Engineering and the European Federation for Medicatl Informatics’ Human and Organizational Factors of Medical Informatics Working Groups |
title_fullStr | Challenges and Best Practices in Ethical Review of Human and Organizational Factors Studies in Health Technology: a Synthesis of Testimonies: A Joint Contribution from the International Medical Informatics Association's Human Factors Engineering and the European Federation for Medicatl Informatics’ Human and Organizational Factors of Medical Informatics Working Groups |
title_full_unstemmed | Challenges and Best Practices in Ethical Review of Human and Organizational Factors Studies in Health Technology: a Synthesis of Testimonies: A Joint Contribution from the International Medical Informatics Association's Human Factors Engineering and the European Federation for Medicatl Informatics’ Human and Organizational Factors of Medical Informatics Working Groups |
title_short | Challenges and Best Practices in Ethical Review of Human and Organizational Factors Studies in Health Technology: a Synthesis of Testimonies: A Joint Contribution from the International Medical Informatics Association's Human Factors Engineering and the European Federation for Medicatl Informatics’ Human and Organizational Factors of Medical Informatics Working Groups |
title_sort | challenges and best practices in ethical review of human and organizational factors studies in health technology: a synthesis of testimonies: a joint contribution from the international medical informatics association's human factors engineering and the european federation for medicatl informatics’ human and organizational factors of medical informatics working groups |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7442520/ https://www.ncbi.nlm.nih.gov/pubmed/32303100 http://dx.doi.org/10.1055/s-0040-1701979 |
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