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Using a knowledge exchange event to assess study participants’ attitudes to research in a rapidly evolving research context
Background: The UK hosts some of the world’s longest-running longitudinal cohort studies, which make repeated observations of their participants and use these data to explore health outcomes. An alternative method for data collection is record linkage; the linking together of electronic health and a...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7361507/ https://www.ncbi.nlm.nih.gov/pubmed/32724860 http://dx.doi.org/10.12688/wellcomeopenres.15651.2 |
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author | Beange, Iona Kirkham, Elizabeth J. Fletcher-Watson, Sue Iveson, Matthew H. Lawrie, Stephen M. Batty, G. David Boardman, James P. Deary, Ian J. Black, Corri Porteous, David J. McIntosh, Andrew M. |
author_facet | Beange, Iona Kirkham, Elizabeth J. Fletcher-Watson, Sue Iveson, Matthew H. Lawrie, Stephen M. Batty, G. David Boardman, James P. Deary, Ian J. Black, Corri Porteous, David J. McIntosh, Andrew M. |
author_sort | Beange, Iona |
collection | PubMed |
description | Background: The UK hosts some of the world’s longest-running longitudinal cohort studies, which make repeated observations of their participants and use these data to explore health outcomes. An alternative method for data collection is record linkage; the linking together of electronic health and administrative records. Applied nationally, this could provide unrivalled opportunities to follow a large number of people in perpetuity. However, public attitudes to the use of data in research are currently unclear. Here we report on an event where we collected attitudes towards recent opportunities and controversies within health data science. Methods: The event was attended by ~250 individuals (cohort members and their guests), who had been invited through the offices of their participating cohort studies. There were a series of presentations describing key research results and the audience participated in 15 multiple-choice questions using interactive voting pads. Results: Our participants showed a high level of trust in researchers (87% scoring them 4/5 or 5/5) and doctors (81%); but less trust in commercial companies (35%). They supported the idea of researchers using information from both neonatal blood spots (Guthrie spots) (97% yes) and from electronic health records (95% yes). Our respondents were willing to wear devices like a ’Fit-bit’ (88% agreed) or take a brain scan that might predict later mental illness (73%). However, they were less willing to take a new drug for research purposes (45%). They were keen to encourage others to take part in research; whether that be offering the opportunity to pregnant mothers (97% agreed) or extending invitations to their own children and grandchildren (98%). Conclusions: Our participants were broadly supportive of research access to data, albeit less supportive when commercial interests were involved. Public engagement events that facilitate two-way interactions can influence and support future research and public engagement efforts. |
format | Online Article Text |
id | pubmed-7361507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-73615072020-07-27 Using a knowledge exchange event to assess study participants’ attitudes to research in a rapidly evolving research context Beange, Iona Kirkham, Elizabeth J. Fletcher-Watson, Sue Iveson, Matthew H. Lawrie, Stephen M. Batty, G. David Boardman, James P. Deary, Ian J. Black, Corri Porteous, David J. McIntosh, Andrew M. Wellcome Open Res Research Article Background: The UK hosts some of the world’s longest-running longitudinal cohort studies, which make repeated observations of their participants and use these data to explore health outcomes. An alternative method for data collection is record linkage; the linking together of electronic health and administrative records. Applied nationally, this could provide unrivalled opportunities to follow a large number of people in perpetuity. However, public attitudes to the use of data in research are currently unclear. Here we report on an event where we collected attitudes towards recent opportunities and controversies within health data science. Methods: The event was attended by ~250 individuals (cohort members and their guests), who had been invited through the offices of their participating cohort studies. There were a series of presentations describing key research results and the audience participated in 15 multiple-choice questions using interactive voting pads. Results: Our participants showed a high level of trust in researchers (87% scoring them 4/5 or 5/5) and doctors (81%); but less trust in commercial companies (35%). They supported the idea of researchers using information from both neonatal blood spots (Guthrie spots) (97% yes) and from electronic health records (95% yes). Our respondents were willing to wear devices like a ’Fit-bit’ (88% agreed) or take a brain scan that might predict later mental illness (73%). However, they were less willing to take a new drug for research purposes (45%). They were keen to encourage others to take part in research; whether that be offering the opportunity to pregnant mothers (97% agreed) or extending invitations to their own children and grandchildren (98%). Conclusions: Our participants were broadly supportive of research access to data, albeit less supportive when commercial interests were involved. Public engagement events that facilitate two-way interactions can influence and support future research and public engagement efforts. F1000 Research Limited 2020-08-28 /pmc/articles/PMC7361507/ /pubmed/32724860 http://dx.doi.org/10.12688/wellcomeopenres.15651.2 Text en Copyright: © 2020 Beange I et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Beange, Iona Kirkham, Elizabeth J. Fletcher-Watson, Sue Iveson, Matthew H. Lawrie, Stephen M. Batty, G. David Boardman, James P. Deary, Ian J. Black, Corri Porteous, David J. McIntosh, Andrew M. Using a knowledge exchange event to assess study participants’ attitudes to research in a rapidly evolving research context |
title | Using a knowledge exchange event to assess study participants’ attitudes to research in a rapidly evolving research context |
title_full | Using a knowledge exchange event to assess study participants’ attitudes to research in a rapidly evolving research context |
title_fullStr | Using a knowledge exchange event to assess study participants’ attitudes to research in a rapidly evolving research context |
title_full_unstemmed | Using a knowledge exchange event to assess study participants’ attitudes to research in a rapidly evolving research context |
title_short | Using a knowledge exchange event to assess study participants’ attitudes to research in a rapidly evolving research context |
title_sort | using a knowledge exchange event to assess study participants’ attitudes to research in a rapidly evolving research context |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7361507/ https://www.ncbi.nlm.nih.gov/pubmed/32724860 http://dx.doi.org/10.12688/wellcomeopenres.15651.2 |
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