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Informed consent for next-generation nucleotide sequencing studies: Aiding communication between participants and investigators
INTRODUCTION: Obtaining informed consent from prospective participants for research studies that include next-generation nucleotide sequencing (NGS) presents significant challenges because of the need to explain all the potential implications of participating, including the possible return of “incid...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471895/ https://www.ncbi.nlm.nih.gov/pubmed/28649453 http://dx.doi.org/10.1017/cts.2016.21 |
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author | Kost, Rhonda G. Poppel, Stephen M. Coller, Barry S. |
author_facet | Kost, Rhonda G. Poppel, Stephen M. Coller, Barry S. |
author_sort | Kost, Rhonda G. |
collection | PubMed |
description | INTRODUCTION: Obtaining informed consent from prospective participants for research studies that include next-generation nucleotide sequencing (NGS) presents significant challenges because of the need to explain all the potential implications of participating, including the possible return of “incidental” findings, in easy-to-understand language. METHODS AND RESULTS: After reviewing the consent processes at other institutions, we decided to supplement the protocol-specific informed consent form with the following: (1) a short pamphlet for the prospective participant that includes a series of questions that she or he is encouraged to ask the investigator, and (2) a more detailed companion guide for investigators to help them develop simple-language answers to the questions. Both documents are available to use or modify. CONCLUSIONS: We propose an approach to obtaining informed consent for NGS studies that encourages discussion of key issues without creating a complex, comprehensive document for participants; it also maximizes investigator flexibility. We also suggest mechanisms to return restricted information to participants. |
format | Online Article Text |
id | pubmed-5471895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54718952017-06-22 Informed consent for next-generation nucleotide sequencing studies: Aiding communication between participants and investigators Kost, Rhonda G. Poppel, Stephen M. Coller, Barry S. J Clin Transl Sci Translational Research, Design and Analysis INTRODUCTION: Obtaining informed consent from prospective participants for research studies that include next-generation nucleotide sequencing (NGS) presents significant challenges because of the need to explain all the potential implications of participating, including the possible return of “incidental” findings, in easy-to-understand language. METHODS AND RESULTS: After reviewing the consent processes at other institutions, we decided to supplement the protocol-specific informed consent form with the following: (1) a short pamphlet for the prospective participant that includes a series of questions that she or he is encouraged to ask the investigator, and (2) a more detailed companion guide for investigators to help them develop simple-language answers to the questions. Both documents are available to use or modify. CONCLUSIONS: We propose an approach to obtaining informed consent for NGS studies that encourages discussion of key issues without creating a complex, comprehensive document for participants; it also maximizes investigator flexibility. We also suggest mechanisms to return restricted information to participants. Cambridge University Press 2017-02-07 /pmc/articles/PMC5471895/ /pubmed/28649453 http://dx.doi.org/10.1017/cts.2016.21 Text en © The Association for Clinical and Translational Science 2017 http://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 licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits noncommercial re-use, distribution, and reproduction in any medium, provided the original work is unaltered and is properly cited. The written permission of Cambridge University Press must be obtained for commercial re-use or in order to create a derivative work. |
spellingShingle | Translational Research, Design and Analysis Kost, Rhonda G. Poppel, Stephen M. Coller, Barry S. Informed consent for next-generation nucleotide sequencing studies: Aiding communication between participants and investigators |
title | Informed consent for next-generation nucleotide sequencing studies: Aiding communication between participants and investigators |
title_full | Informed consent for next-generation nucleotide sequencing studies: Aiding communication between participants and investigators |
title_fullStr | Informed consent for next-generation nucleotide sequencing studies: Aiding communication between participants and investigators |
title_full_unstemmed | Informed consent for next-generation nucleotide sequencing studies: Aiding communication between participants and investigators |
title_short | Informed consent for next-generation nucleotide sequencing studies: Aiding communication between participants and investigators |
title_sort | informed consent for next-generation nucleotide sequencing studies: aiding communication between participants and investigators |
topic | Translational Research, Design and Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471895/ https://www.ncbi.nlm.nih.gov/pubmed/28649453 http://dx.doi.org/10.1017/cts.2016.21 |
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