Literature DB >> 21478424

Achieving online consent to participation in large-scale gene-environment studies: a tangible destination.

Fiona Wood1, Jenny Kowalczuk, Glyn Elwyn, Clive Mitchell, John Gallacher.   

Abstract

BACKGROUND: Population based genetics studies are dependent on large numbers of individuals in the pursuit of small effect sizes. Recruiting and consenting a large number of participants is both costly and time consuming. We explored whether an online consent process for large-scale genetics studies is acceptable for prospective participants using an example online genetics study.
METHODS: We conducted semi-structured interviews with 42 members of the public stratified by age group, gender and newspaper readership (a measure of social status). Respondents were asked to use a website designed to recruit for a large-scale genetic study. After using the website a semi-structured interview was conducted to explore opinions and any issues they would have. Responses were analysed using thematic content analysis.
RESULTS: The majority of respondents said they would take part in the research (32/42). Those who said they would decline to participate saw fewer benefits from the research, wanted more information and expressed a greater number of concerns about the study. Younger respondents had concerns over time commitment. Middle aged respondents were concerned about privacy and security. Older respondents were more altruistic in their motivation to participate. Common themes included trust in the authenticity of the website, security of personal data, curiosity about their own genetic profile, operational concerns and a desire for more information about the research.
CONCLUSIONS: Online consent to large-scale genetic studies is likely to be acceptable to the public. The online consent process must establish trust quickly and effectively by asserting authenticity and credentials, and provide access to a range of information to suit different information preferences.

Entities:  

Mesh:

Year:  2011        PMID: 21478424     DOI: 10.1136/jme.2010.040352

Source DB:  PubMed          Journal:  J Med Ethics        ISSN: 0306-6800            Impact factor:   2.903


  11 in total

1.  Generating large-scale longitudinal data resources for aging research.

Authors:  John Gallacher; Scott M Hofer
Journal:  J Gerontol B Psychol Sci Soc Sci       Date:  2011-07       Impact factor: 4.077

2.  Community-based partnership to identify keys to biospecimen research participation.

Authors:  Deborah O Erwin; Kirsten Moysich; Marc T Kiviniemi; Frances G Saad-Harfouche; Warren Davis; Nikia Clark-Hargrave; Gregory L Ciupak; Christine B Ambrosone; Charles Walker
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Review 3.  Stakeholders' perspectives on biobank-based genomic research: systematic review of the literature.

Authors:  Alma Husedzinovic; Dominik Ose; Christoph Schickhardt; Stefan Fröhling; Eva C Winkler
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4.  Online Education and e-Consent for GeneScreen, a Preventive Genomic Screening Study.

Authors:  R Jean Cadigan; Rita Butterfield; Christine Rini; Margaret Waltz; Kristine J Kuczynski; Kristin Muessig; Katrina A B Goddard; Gail E Henderson
Journal:  Public Health Genomics       Date:  2017-10-26       Impact factor: 2.000

5.  Pilot intervention outcomes of an educational program for biospecimen research participation.

Authors:  Marc T Kiviniemi; Frances G Saad-Harfouche; Gregory L Ciupak; Warren Davis; Kirsten Moysich; Nikia Clark Hargrave; Christine B Ambrosone; Charles Walker; Deborah O Erwin
Journal:  J Cancer Educ       Date:  2013-03       Impact factor: 2.037

6.  Patient characteristics and participation in a genetic study: a type 2 diabetes cohort.

Authors:  Loabat Amiri; Andrea E Cassidy-Bushrow; Heather Dakki; Jia Li; Karen Wells; Susan A Oliveria; Marianne Ulcickas Yood; Abraham Thomas; David E Lanfear
Journal:  J Investig Med       Date:  2014-01       Impact factor: 2.895

7.  Recruitment and Participation of Recreational Runners in a Large Epidemiological and Genetic Research Study: Retrospective Data Analysis.

Authors:  Silvia Manzanero; Maria Kozlovskaia; Nicole Vlahovich; David C Hughes
Journal:  JMIR Res Protoc       Date:  2018-05-23

8.  Online Consent Enables a Randomized, Controlled Trial Testing a Patient-Centered Online Decision-Aid for Medicare Beneficiaries to Meet Recruitment Goal in Short Time Frame.

Authors:  Amy Meehan; Mary Kate Bundorf; Roman Klimke; Cheryl D Stults; Albert S Chan; Ting Pun; Ming Tai-Seale
Journal:  J Patient Exp       Date:  2019-11-26

9.  'Sifting the significance from the data' - the impact of high-throughput genomic technologies on human genetics and health care.

Authors:  Angus J Clarke; David N Cooper; Michael Krawczak; Chris Tyler-Smith; Helen M Wallace; Andrew O M Wilkie; Frances Lucy Raymond; Ruth Chadwick; Nick Craddock; Ros John; John Gallacher; Mathias Chiano
Journal:  Hum Genomics       Date:  2012-08-02       Impact factor: 4.639

10.  A platform for the remote conduct of gene-environment interaction studies.

Authors:  John Gallacher; Rory Collins; Paul Elliott; Stephen Palmer; Paul Burton; Clive Mitchell; Gareth John; Ronan Lyons
Journal:  PLoS One       Date:  2013-01-18       Impact factor: 3.240

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