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Written Informed Consent for Participation in a Study and Reduction in Consent Rate
BACKGROUND: The association between the method of obtaining informed consent and the consent rate in a cohort study, as well as the differences between consenters and non-consenters with regard to blood-sample donation are unclear. METHODS: We measured the consent rates among 64-year-old residents w...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japan Epidemiological Association
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4771614/ https://www.ncbi.nlm.nih.gov/pubmed/19039193 http://dx.doi.org/10.2188/jea.JE2008011 |
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author | Tamakoshi, Akiko Kawamura, Takashi Wakai, Kenji Ando, Masahiko |
author_facet | Tamakoshi, Akiko Kawamura, Takashi Wakai, Kenji Ando, Masahiko |
author_sort | Tamakoshi, Akiko |
collection | PubMed |
description | BACKGROUND: The association between the method of obtaining informed consent and the consent rate in a cohort study, as well as the differences between consenters and non-consenters with regard to blood-sample donation are unclear. METHODS: We measured the consent rates among 64-year-old residents who underwent medical checkups in a city for a cohort study consisting of a questionnaire survey and blood-sample donation and determined the influence of different approaches to informed consent and the participants’ characteristics on the consent rates. RESULTS: Of 3,098 residents who underwent medical checkups over 10 years, 99.2% responded to the questionnaire survey, and 92.5% agreed to blood-sample donation. The consent rate for blood-sample donation after obtaining individual written informed consent was lower than that observed with the general-announcement approach. Differences in the consent rates for participation in the questionnaire study were, however, negligible. A higher percentage of men than women consented to donate blood samples. After adjustments for gender, it was observed that individuals with a history of hypertension and those without depression consented to blood-sample donation significantly more frequently. CONCLUSION: The consent rate for blood-sample donation to the study decreased when the opt-in approach with written consent was used. This decrease may introduce consent bias, and the method of obtaining informed consent should be revised. |
format | Online Article Text |
id | pubmed-4771614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Japan Epidemiological Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-47716142016-03-03 Written Informed Consent for Participation in a Study and Reduction in Consent Rate Tamakoshi, Akiko Kawamura, Takashi Wakai, Kenji Ando, Masahiko J Epidemiol Short Communication BACKGROUND: The association between the method of obtaining informed consent and the consent rate in a cohort study, as well as the differences between consenters and non-consenters with regard to blood-sample donation are unclear. METHODS: We measured the consent rates among 64-year-old residents who underwent medical checkups in a city for a cohort study consisting of a questionnaire survey and blood-sample donation and determined the influence of different approaches to informed consent and the participants’ characteristics on the consent rates. RESULTS: Of 3,098 residents who underwent medical checkups over 10 years, 99.2% responded to the questionnaire survey, and 92.5% agreed to blood-sample donation. The consent rate for blood-sample donation after obtaining individual written informed consent was lower than that observed with the general-announcement approach. Differences in the consent rates for participation in the questionnaire study were, however, negligible. A higher percentage of men than women consented to donate blood samples. After adjustments for gender, it was observed that individuals with a history of hypertension and those without depression consented to blood-sample donation significantly more frequently. CONCLUSION: The consent rate for blood-sample donation to the study decreased when the opt-in approach with written consent was used. This decrease may introduce consent bias, and the method of obtaining informed consent should be revised. Japan Epidemiological Association 2008-12-17 /pmc/articles/PMC4771614/ /pubmed/19039193 http://dx.doi.org/10.2188/jea.JE2008011 Text en © 2008 Japan Epidemiological Association. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Short Communication Tamakoshi, Akiko Kawamura, Takashi Wakai, Kenji Ando, Masahiko Written Informed Consent for Participation in a Study and Reduction in Consent Rate |
title | Written Informed Consent for Participation in a Study and Reduction in Consent Rate |
title_full | Written Informed Consent for Participation in a Study and Reduction in Consent Rate |
title_fullStr | Written Informed Consent for Participation in a Study and Reduction in Consent Rate |
title_full_unstemmed | Written Informed Consent for Participation in a Study and Reduction in Consent Rate |
title_short | Written Informed Consent for Participation in a Study and Reduction in Consent Rate |
title_sort | written informed consent for participation in a study and reduction in consent rate |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4771614/ https://www.ncbi.nlm.nih.gov/pubmed/19039193 http://dx.doi.org/10.2188/jea.JE2008011 |
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