Literature DB >> 33563268

Adding dynamic consent to a longitudinal cohort study: A qualitative study of EXCEED participant perspectives.

Susan E Wallace1, José Miola2.   

Abstract

BACKGROUND: Dynamic consent has been proposed as a process through which participants and patients can gain more control over how their data and samples, donated for biomedical research, are used, resulting in greater trust in researchers. It is also a way to respond to evolving data protection frameworks and new legislation. Others argue that the broad consent currently used in biobank research is ethically robust. Little empirical research with cohort study participants has been published. This research investigated the participants' opinions of adding a dynamic consent interface to their existing study.
METHODS: Adult participants in the Extended Cohort for E-health, Environment and DNA (EXCEED) longitudinal cohort study who are members of the EXCEED Public and Participant Engagement Group were recruited. Four focus groups were conducted and analysed for thematic content. Discussion topics were derived from a review of the current literature on dynamic consent.
RESULTS: Participants were in favour of many aspects of a dynamic consent interface, such as being able to update their information, add additional data to their records and choose withdrawal options. They were supportive provided it was simple to use and not intrusive. Participants expressed a markedly high level of trust in the study and its investigators and were unanimously happy with their current participation. No strong support was found for adding a dynamic consent interface to EXCEED.
CONCLUSIONS: Trust in the study researchers was the strongest theme found. Openness and good data security were needed to retain their trust. While happy to discuss dynamic consent, participants were satisfied with the current study arrangements. There were indications that changing the study might unnecessarily disturb their trust. This raised the question of whether there are contexts where dynamic consent is more appropriate than others. This study was limited by the small number of participants who were committed to the study and biased towards it. More research is needed to fully understand the potential impact of adding a dynamic consent interface to an existing cohort study.

Entities:  

Keywords:  Biobank; Biomedical research; Data protection; Dynamic consent; Longitudinal cohort studies

Mesh:

Year:  2021        PMID: 33563268      PMCID: PMC7874652          DOI: 10.1186/s12910-021-00583-w

Source DB:  PubMed          Journal:  BMC Med Ethics        ISSN: 1472-6939            Impact factor:   2.652


  23 in total

1.  Broadening consent--and diluting ethics?

Authors:  B Hofmann
Journal:  J Med Ethics       Date:  2009-02       Impact factor: 2.903

Review 2.  From patients to partners: participant-centric initiatives in biomedical research.

Authors:  Jane Kaye; Liam Curren; Nick Anderson; Kelly Edwards; Stephanie M Fullerton; Nadja Kanellopoulou; David Lund; Daniel G MacArthur; Deborah Mascalzoni; James Shepherd; Patrick L Taylor; Sharon F Terry; Stefan F Winter
Journal:  Nat Rev Genet       Date:  2012-04-03       Impact factor: 53.242

3.  Australian Aboriginal and Torres Strait Islander Collections of Genetic Heritage: The Legal, Ethical and Practical Considerations of a Dynamic Consent Approach to Decision Making.

Authors:  Megan Prictor; Sharon Huebner; Harriet J A Teare; Luke Burchill; Jane Kaye
Journal:  J Law Med Ethics       Date:  2020-03       Impact factor: 1.718

4.  UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age.

Authors:  Cathie Sudlow; John Gallacher; Naomi Allen; Valerie Beral; Paul Burton; John Danesh; Paul Downey; Paul Elliott; Jane Green; Martin Landray; Bette Liu; Paul Matthews; Giok Ong; Jill Pell; Alan Silman; Alan Young; Tim Sprosen; Tim Peakman; Rory Collins
Journal:  PLoS Med       Date:  2015-03-31       Impact factor: 11.069

5.  Broad consent versus dynamic consent in biobank research: is passive participation an ethical problem?

Authors:  Kristin Solum Steinsbekk; Bjørn Kåre Myskja; Berge Solberg
Journal:  Eur J Hum Genet       Date:  2013-01-09       Impact factor: 4.246

6.  Dynamic consent: a possible solution to improve patient confidence and trust in how electronic patient records are used in medical research.

Authors:  Hawys Williams; Karen Spencer; Caroline Sanders; David Lund; Edgar A Whitley; Jane Kaye; William G Dixon
Journal:  JMIR Med Inform       Date:  2015-01-13

7.  The RUDY study platform - a novel approach to patient driven research in rare musculoskeletal diseases.

Authors:  M K Javaid; L Forestier-Zhang; L Watts; A Turner; C Ponte; H Teare; D Gray; N Gray; R Popert; J Hogg; J Barrett; R Pinedo-Villanueva; C Cooper; R Eastell; N Bishop; R Luqmani; P Wordsworth; J Kaye
Journal:  Orphanet J Rare Dis       Date:  2016-11-08       Impact factor: 4.123

8.  Assessing the stability of biobank donor preferences regarding sample use: evidence supporting the value of dynamic consent.

Authors:  Joel E Pacyna; Jennifer B McCormick; Janet E Olson; Erin M Winkler; Josh T Bublitz; Matthew A Hathcock; Richard R Sharp
Journal:  Eur J Hum Genet       Date:  2020-04-23       Impact factor: 4.246

9.  DNA databanks and consent: a suggested policy option involving an authorization model.

Authors:  Timothy Caulfield; Ross E G Upshur; Abdallah Daar
Journal:  BMC Med Ethics       Date:  2003-01-03       Impact factor: 2.652

10.  The Cooperative Health Research in South Tyrol (CHRIS) study: rationale, objectives, and preliminary results.

Authors:  Cristian Pattaro; Martin Gögele; Deborah Mascalzoni; Roberto Melotti; Christine Schwienbacher; Alessandro De Grandi; Luisa Foco; Yuri D'Elia; Barbara Linder; Christian Fuchsberger; Cosetta Minelli; Clemens Egger; Lisa S Kofink; Stefano Zanigni; Torsten Schäfer; Maurizio F Facheris; Sigurður V Smárason; Alessandra Rossini; Andrew A Hicks; Helmuth Weiss; Peter P Pramstaller
Journal:  J Transl Med       Date:  2015-11-05       Impact factor: 5.531

View more
  1 in total

1.  Ethical issues in biomedical research using electronic health records: a systematic review.

Authors:  Jan Piasecki; Ewa Walkiewicz-Żarek; Justyna Figas-Skrzypulec; Anna Kordecka; Vilius Dranseika
Journal:  Med Health Care Philos       Date:  2021-06-19
  1 in total

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