Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/37263
Appears in Collections:Faculty of Health Sciences and Sport Journal Articles
Peer Review Status: Refereed
Title: 'To me, it's ones and zeros, but in reality that one is death': A qualitative study exploring researchers' experience of involving and engaging seldom-heard communities in big data research
Author(s): Teodorowski, Piotr
Rodgers, Sarah E
Fleming, Kate
Tahir, Naheed
Ahmed, Saiqa
Frith, Lucy
Contact Email: piotr.teodorowski@stir.ac.uk
Keywords: big data
PPI
public engagement
public involvement
qualitative
seldom-heard
Issue Date: Apr-2023
Date Deposited: 24-Jul-2025
Citation: Teodorowski P, Rodgers SE, Fleming K, Tahir N, Ahmed S & Frith L (2023) 'To me, it's ones and zeros, but in reality that one is death': A qualitative study exploring researchers' experience of involving and engaging seldom-heard communities in big data research. <i>Health Expectations</i>, 26 (2), pp. 882-891. https://doi.org/10.1111/hex.13713
Abstract: Background Big data research requires public support. It has been argued that this can be achieved by public involvement and engagement to ensure that public views are at the centre of research projects. Researchers should aim to include diverse communities, including seldom-heard voices, to ensure that a range of voices are heard and that research is meaningful to them. Objective We explored how researchers involve and engage seldom-heard communities around big data research. Methods This is a qualitative study. Researchers who had experience of involving or engaging seldom-heard communities in big data research were recruited. They were based in England (n = 5), Scotland (n = 4), Belgium (n = 2) and Canada (n = 1). Twelve semistructured interviews were conducted on Zoom. All interviews were audio-recorded and transcribed, and we used reflexive thematic analysis to analyse participants' experiences. Results The analysis highlighted the complexity of involving and engaging seldom-heard communities around big data research. Four themes were developed to represent participants' experiences: (1) abstraction and complexity of big data, (2) one size does not fit all, (3) working in partnership and (4) empowering the public contribution. Conclusion The study offers researchers a better understanding of how to involve and engage seldom-heard communities in a meaningful way around big data research. There is no one right approach, with involvement and engagement activities required to be project-specific and dependent on the public contributors, researchers' needs, resources and time available.
DOI Link: 10.1111/hex.13713
Rights: © 2023 The Authors. Health Expectations published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Licence URL(s): http://creativecommons.org/licenses/by/4.0/

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