Collecting and sharing self-generated health and lifestyle data: understanding barriers for people living with long-term health conditions – a survey study

Brown, Richard, Coventry, Lynne, Sillence, Elizabeth, Blythe, John, Stumpf, Simone, Lloyd, Karen, Gibbs, Jo, Tariq, Shema, Bird, Jon and Durrant, Abigail (2022) Collecting and sharing self-generated health and lifestyle data: understanding barriers for people living with long-term health conditions – a survey study. Digital Health, 8. p. 205520762210844. ISSN 2055-2076

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Official URL: https://doi.org/10.1177/20552076221084458

Abstract

Background: The growing popularity of collecting self-generated health and lifestyle data presents a valuable opportunity to develop our understanding of long-term health conditions (LTHCs) and improve care. Barriers remain to the effective sharing of health and lifestyle data by those living with LTHCs which include beliefs around concepts of Trust, Identity, Privacy and Security (TIPS), experiences of stigma, perceptions of risk and information sensitivity.Method:We surveyed 250 UK adults who reported living with a range of LTHCs. We recorded data to assess self-reported behaviours, experiences, attitudes and motivations relevant to sharing self-generated health and lifestyle data. We also asked participants about their beliefs about TIPS, stigma, and perceptions of risk and information sensitivity regarding their health and lifestyle data.Results: Three quarters of our sample reported recording information about their health and lifestyle on a daily basis. However two thirds reported never or rarely sharing this information with others. TIPS concerns were considered to be ‘very important’ by those with LTHCs when deciding whether or not to share self-generated health and lifestyle data with others, with security concerns considered most important. Of those living with a LTHC, 58 reported experiencing stigma associated with their condition. The greatest perceived risk from sharing with others was the potential for future harm to their social relationships.Conclusions:Our findings suggest that, in order for health professionals and researchers to benefit from the increased prevalence of self-generated health and lifestyle data, more can be done to address security concerns and to understand perceived risks associated with data sharing. Digital platforms aimed at facilitating the sharing of self-generated health and lifestyle data may look to highlight security features, enable users to control the sharing of certain information types, and emphasise the practical benefits to users of sharing health and lifestyle data with others.

Item Type: Article
Additional Information: Funding information: This study has been conducted as part of a UK EPSRC funded programme ("INTUIT: Interaction Design for Trusted Sharing of Personal Health Data to Live Well with HIV", 2020; EP/R033900/2), examining TIPS concerns around the sharing of self-generated health and lifestyle data primarily among people living with HIV but also for those with other potentially stigmatised conditions. This work is funded by the EPSRC, grant number EP/R033900/1.
Uncontrolled Keywords: Disease, public health, eHealth, personalised medicine, digital health, self-generated health and lifestyle data, psychology, risk perceptions, health communications
Subjects: B900 Others in Subjects allied to Medicine
G500 Information Systems
Department: Faculties > Health and Life Sciences > Psychology
Depositing User: John Coen
Date Deposited: 16 Feb 2022 12:15
Last Modified: 08 Mar 2022 13:45
URI: http://nrl.northumbria.ac.uk/id/eprint/48483

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