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Obtaining subjects’ consent to publish identifying personal information: current practices and identifying potential issues
BACKGROUND: In studies publishing identifying personal information, obtaining consent is regarded as necessary, as it is impossible to ensure complete anonymity. However, current journal practices around specific points to consider when obtaining consent, the contents of consent forms and how consen...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222768/ https://www.ncbi.nlm.nih.gov/pubmed/24267590 http://dx.doi.org/10.1186/1472-6939-14-47 |
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author | Yoshida, Akiko Dowa, Yuri Murakami, Hiromi Kosugi, Shinji |
author_facet | Yoshida, Akiko Dowa, Yuri Murakami, Hiromi Kosugi, Shinji |
author_sort | Yoshida, Akiko |
collection | PubMed |
description | BACKGROUND: In studies publishing identifying personal information, obtaining consent is regarded as necessary, as it is impossible to ensure complete anonymity. However, current journal practices around specific points to consider when obtaining consent, the contents of consent forms and how consent forms are managed have not yet been fully examined. This study was conducted to identify potential issues surrounding consent to publish identifying personal information. METHODS: Content analysis was carried out on instructions for authors and consent forms developed by academic journals in four fields (as classified by Journal Citation Reports): medicine general and internal, genetics and heredity, pediatrics, and psychiatry. An online questionnaire survey of editors working for journals that require the submission of consent forms was also conducted. RESULTS: Instructions for authors were reviewed for 491 academic journals (132 for medicine general and internal, 147 for genetics and heredity, 100 for pediatrics, and 112 for psychiatry). Approximately 40% (203: 74 for medicine general and internal, 31 for genetics and heredity, 58 for pediatrics, and 40 for psychiatry) stated that subject consent was necessary. The submission of consent forms was required by 30% (154) of the journals studied, and 10% (50) provided their own consent forms for authors to use. Two journals mentioned that the possible effects of publication on subjects should be considered. Many journal consent forms mentioned the difficulties in ensuring complete anonymity of subjects, but few addressed the study objective, the subjects’ right to refuse consent and the withdrawal of consent. The main reason for requiring the submission of consent forms was to confirm that consent had been obtained. CONCLUSION: Approximately 40% of journals required subject consent to be obtained. However, differences were observed depending on the fields. Specific considerations were not always documented. There is a need to address issues around the study objective, subjects’ right to refuse consent and the withdrawal of consent. Whether responsibility for ensuring that the consent form has been signed lies with publishers also needs to be discussed. |
format | Online Article Text |
id | pubmed-4222768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42227682014-11-07 Obtaining subjects’ consent to publish identifying personal information: current practices and identifying potential issues Yoshida, Akiko Dowa, Yuri Murakami, Hiromi Kosugi, Shinji BMC Med Ethics Research Article BACKGROUND: In studies publishing identifying personal information, obtaining consent is regarded as necessary, as it is impossible to ensure complete anonymity. However, current journal practices around specific points to consider when obtaining consent, the contents of consent forms and how consent forms are managed have not yet been fully examined. This study was conducted to identify potential issues surrounding consent to publish identifying personal information. METHODS: Content analysis was carried out on instructions for authors and consent forms developed by academic journals in four fields (as classified by Journal Citation Reports): medicine general and internal, genetics and heredity, pediatrics, and psychiatry. An online questionnaire survey of editors working for journals that require the submission of consent forms was also conducted. RESULTS: Instructions for authors were reviewed for 491 academic journals (132 for medicine general and internal, 147 for genetics and heredity, 100 for pediatrics, and 112 for psychiatry). Approximately 40% (203: 74 for medicine general and internal, 31 for genetics and heredity, 58 for pediatrics, and 40 for psychiatry) stated that subject consent was necessary. The submission of consent forms was required by 30% (154) of the journals studied, and 10% (50) provided their own consent forms for authors to use. Two journals mentioned that the possible effects of publication on subjects should be considered. Many journal consent forms mentioned the difficulties in ensuring complete anonymity of subjects, but few addressed the study objective, the subjects’ right to refuse consent and the withdrawal of consent. The main reason for requiring the submission of consent forms was to confirm that consent had been obtained. CONCLUSION: Approximately 40% of journals required subject consent to be obtained. However, differences were observed depending on the fields. Specific considerations were not always documented. There is a need to address issues around the study objective, subjects’ right to refuse consent and the withdrawal of consent. Whether responsibility for ensuring that the consent form has been signed lies with publishers also needs to be discussed. BioMed Central 2013-11-25 /pmc/articles/PMC4222768/ /pubmed/24267590 http://dx.doi.org/10.1186/1472-6939-14-47 Text en Copyright © 2013 Yoshida et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Yoshida, Akiko Dowa, Yuri Murakami, Hiromi Kosugi, Shinji Obtaining subjects’ consent to publish identifying personal information: current practices and identifying potential issues |
title | Obtaining subjects’ consent to publish identifying personal information: current practices and identifying potential issues |
title_full | Obtaining subjects’ consent to publish identifying personal information: current practices and identifying potential issues |
title_fullStr | Obtaining subjects’ consent to publish identifying personal information: current practices and identifying potential issues |
title_full_unstemmed | Obtaining subjects’ consent to publish identifying personal information: current practices and identifying potential issues |
title_short | Obtaining subjects’ consent to publish identifying personal information: current practices and identifying potential issues |
title_sort | obtaining subjects’ consent to publish identifying personal information: current practices and identifying potential issues |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222768/ https://www.ncbi.nlm.nih.gov/pubmed/24267590 http://dx.doi.org/10.1186/1472-6939-14-47 |
work_keys_str_mv | AT yoshidaakiko obtainingsubjectsconsenttopublishidentifyingpersonalinformationcurrentpracticesandidentifyingpotentialissues AT dowayuri obtainingsubjectsconsenttopublishidentifyingpersonalinformationcurrentpracticesandidentifyingpotentialissues AT murakamihiromi obtainingsubjectsconsenttopublishidentifyingpersonalinformationcurrentpracticesandidentifyingpotentialissues AT kosugishinji obtainingsubjectsconsenttopublishidentifyingpersonalinformationcurrentpracticesandidentifyingpotentialissues |