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Readability of informed consent forms for whole-exome and whole-genome sequencing
Whole-exome and whole-genome sequencing (WES, WGS) can generate an unprecedented amount of complex information, making the informed consent (IC) process challenging. The aim of our study was to assess the readability of English IC forms for clinical whole-exome and whole-genome sequencing using the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849699/ https://www.ncbi.nlm.nih.gov/pubmed/28856579 http://dx.doi.org/10.1007/s12687-017-0324-6 |
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author | Niemiec, Emilia Vears, Danya F. Borry, Pascal Howard, Heidi Carmen |
author_facet | Niemiec, Emilia Vears, Danya F. Borry, Pascal Howard, Heidi Carmen |
author_sort | Niemiec, Emilia |
collection | PubMed |
description | Whole-exome and whole-genome sequencing (WES, WGS) can generate an unprecedented amount of complex information, making the informed consent (IC) process challenging. The aim of our study was to assess the readability of English IC forms for clinical whole-exome and whole-genome sequencing using the SMOG and Flesch-Kincaid formulas. We analysed 36 forms, most of which were from US providers. The median readability grade levels were 14.75 (the SMOG formula) and 12.2 (the Flesch-Kincaid formula); these values indicate the years of education after which a person would be able to understand a text studied. All forms studied seem to fail to meet the average recommended readability grade level of 8 (e.g. by Institutional Review Boards of US medical schools) for IC forms, indicating that the content of the forms may not be comprehensible to many patients. The sections aimed at health care professionals (HCPs) in the forms indicate that HCPs should be responsible for explaining IC information to the patients. However, WES and WGS may be increasingly offered by primary care professionals who may not (yet) have sufficient training to be able to communicate effectively with patients about genomics. Therefore, to secure an adequate, truly informed consent process, the task of developing good, legible examples of IC forms along with educating HCPs in genomics should be taken seriously, and adequate resources should be allocated to enable these tasks. |
format | Online Article Text |
id | pubmed-5849699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-58496992018-03-21 Readability of informed consent forms for whole-exome and whole-genome sequencing Niemiec, Emilia Vears, Danya F. Borry, Pascal Howard, Heidi Carmen J Community Genet Original Article Whole-exome and whole-genome sequencing (WES, WGS) can generate an unprecedented amount of complex information, making the informed consent (IC) process challenging. The aim of our study was to assess the readability of English IC forms for clinical whole-exome and whole-genome sequencing using the SMOG and Flesch-Kincaid formulas. We analysed 36 forms, most of which were from US providers. The median readability grade levels were 14.75 (the SMOG formula) and 12.2 (the Flesch-Kincaid formula); these values indicate the years of education after which a person would be able to understand a text studied. All forms studied seem to fail to meet the average recommended readability grade level of 8 (e.g. by Institutional Review Boards of US medical schools) for IC forms, indicating that the content of the forms may not be comprehensible to many patients. The sections aimed at health care professionals (HCPs) in the forms indicate that HCPs should be responsible for explaining IC information to the patients. However, WES and WGS may be increasingly offered by primary care professionals who may not (yet) have sufficient training to be able to communicate effectively with patients about genomics. Therefore, to secure an adequate, truly informed consent process, the task of developing good, legible examples of IC forms along with educating HCPs in genomics should be taken seriously, and adequate resources should be allocated to enable these tasks. Springer Berlin Heidelberg 2017-08-31 2018-04 /pmc/articles/PMC5849699/ /pubmed/28856579 http://dx.doi.org/10.1007/s12687-017-0324-6 Text en © The Author(s) 2017 Open Access This 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. |
spellingShingle | Original Article Niemiec, Emilia Vears, Danya F. Borry, Pascal Howard, Heidi Carmen Readability of informed consent forms for whole-exome and whole-genome sequencing |
title | Readability of informed consent forms for whole-exome and whole-genome sequencing |
title_full | Readability of informed consent forms for whole-exome and whole-genome sequencing |
title_fullStr | Readability of informed consent forms for whole-exome and whole-genome sequencing |
title_full_unstemmed | Readability of informed consent forms for whole-exome and whole-genome sequencing |
title_short | Readability of informed consent forms for whole-exome and whole-genome sequencing |
title_sort | readability of informed consent forms for whole-exome and whole-genome sequencing |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849699/ https://www.ncbi.nlm.nih.gov/pubmed/28856579 http://dx.doi.org/10.1007/s12687-017-0324-6 |
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