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Developing the ethics of implementation research in health

Implementation research (IR) is growing in recognition as an important generator of practical knowledge that can be translated into health policy. With its aim to answer questions about how to improve access to interventions that have been shown to work but have not reached many of the people who co...

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Autores principales: Gopichandran, Vijayaprasad, Luyckx, Valerie A., Biller-Andorno, Nikola, Fairchild, Amy, Singh, Jerome, Tran, Nhan, Saxena, Abha, Launois, Pascal, Reis, Andreas, Maher, Dermot, Vahedi, Mahnaz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5148832/
https://www.ncbi.nlm.nih.gov/pubmed/27938400
http://dx.doi.org/10.1186/s13012-016-0527-y
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author Gopichandran, Vijayaprasad
Luyckx, Valerie A.
Biller-Andorno, Nikola
Fairchild, Amy
Singh, Jerome
Tran, Nhan
Saxena, Abha
Launois, Pascal
Reis, Andreas
Maher, Dermot
Vahedi, Mahnaz
author_facet Gopichandran, Vijayaprasad
Luyckx, Valerie A.
Biller-Andorno, Nikola
Fairchild, Amy
Singh, Jerome
Tran, Nhan
Saxena, Abha
Launois, Pascal
Reis, Andreas
Maher, Dermot
Vahedi, Mahnaz
author_sort Gopichandran, Vijayaprasad
collection PubMed
description Implementation research (IR) is growing in recognition as an important generator of practical knowledge that can be translated into health policy. With its aim to answer questions about how to improve access to interventions that have been shown to work but have not reached many of the people who could benefit from them, IR involves a range of particular ethical considerations that have not yet been comprehensively covered in international guidelines on health research ethics. The fundamental ethical principles governing clinical research apply equally in IR, but the application of these principles may differ depending on the IR question, context, and the nature of the proposed intervention. IR questions cover a broad range of topics that focus on improving health system functioning and improving equitable and just access to effective health care interventions. As such, IR designs are flexible and often innovative, and ethical principles cannot simply be extrapolated from their applications in clinical research. Meaningful engagement with all stakeholders including communities and research participants is a fundamental ethical requirement that cuts across all study phases of IR and links most ethical concerns. Careful modification of the informed consent process may be required in IR to permit study of a needed intervention. The risks associated with IR may be difficult to anticipate and may be very context-specific. The benefits of IR may not accrue to the same groups who participate in the research, therefore justifying the risks versus benefits of IR may be ethically challenging. The expectation that knowledge generated through IR should be rapidly translated into health policy and practice necessitates up-front commitments from decision-makers to sustainability and scalability of effective interventions. Greater awareness of the particular ethical implications of the features of IR is urgently needed to facilitate optimal ethical conduct of IR and uniform ethical review.
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spelling pubmed-51488322016-12-15 Developing the ethics of implementation research in health Gopichandran, Vijayaprasad Luyckx, Valerie A. Biller-Andorno, Nikola Fairchild, Amy Singh, Jerome Tran, Nhan Saxena, Abha Launois, Pascal Reis, Andreas Maher, Dermot Vahedi, Mahnaz Implement Sci Debate Implementation research (IR) is growing in recognition as an important generator of practical knowledge that can be translated into health policy. With its aim to answer questions about how to improve access to interventions that have been shown to work but have not reached many of the people who could benefit from them, IR involves a range of particular ethical considerations that have not yet been comprehensively covered in international guidelines on health research ethics. The fundamental ethical principles governing clinical research apply equally in IR, but the application of these principles may differ depending on the IR question, context, and the nature of the proposed intervention. IR questions cover a broad range of topics that focus on improving health system functioning and improving equitable and just access to effective health care interventions. As such, IR designs are flexible and often innovative, and ethical principles cannot simply be extrapolated from their applications in clinical research. Meaningful engagement with all stakeholders including communities and research participants is a fundamental ethical requirement that cuts across all study phases of IR and links most ethical concerns. Careful modification of the informed consent process may be required in IR to permit study of a needed intervention. The risks associated with IR may be difficult to anticipate and may be very context-specific. The benefits of IR may not accrue to the same groups who participate in the research, therefore justifying the risks versus benefits of IR may be ethically challenging. The expectation that knowledge generated through IR should be rapidly translated into health policy and practice necessitates up-front commitments from decision-makers to sustainability and scalability of effective interventions. Greater awareness of the particular ethical implications of the features of IR is urgently needed to facilitate optimal ethical conduct of IR and uniform ethical review. BioMed Central 2016-12-09 /pmc/articles/PMC5148832/ /pubmed/27938400 http://dx.doi.org/10.1186/s13012-016-0527-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Debate
Gopichandran, Vijayaprasad
Luyckx, Valerie A.
Biller-Andorno, Nikola
Fairchild, Amy
Singh, Jerome
Tran, Nhan
Saxena, Abha
Launois, Pascal
Reis, Andreas
Maher, Dermot
Vahedi, Mahnaz
Developing the ethics of implementation research in health
title Developing the ethics of implementation research in health
title_full Developing the ethics of implementation research in health
title_fullStr Developing the ethics of implementation research in health
title_full_unstemmed Developing the ethics of implementation research in health
title_short Developing the ethics of implementation research in health
title_sort developing the ethics of implementation research in health
topic Debate
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5148832/
https://www.ncbi.nlm.nih.gov/pubmed/27938400
http://dx.doi.org/10.1186/s13012-016-0527-y
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