The perceptions of social and information privacy risks of Inflammatory Bowel Disease patients using social media platforms for health-related support

• URL: http://arxiv.org/abs/2008.03541v1
• Date: Sat, 8 Aug 2020 15:31:23 GMT
• Title: The perceptions of social and information privacy risks of Inflammatory Bowel Disease patients using social media platforms for health-related support
• Authors: Kate O'Leary, Elvira Perez Vallejos, Neil Coulson, Derek McAuley
• Abstract summary: We conducted interviews with 38 patients with inflammatory bowel disease (IBD) using social media platforms to engage with online communities. We identified that patients typically demonstrate the privacy and risk dual calculus for perceived social privacy concerns. Our findings illustrate the different levels of understanding between social and information privacy and the impacts on how individuals take agency over their personal data.
• Score: 4.349068560043031
• License: http://creativecommons.org/licenses/by-nc-sa/4.0/
• Abstract: With hundreds of thousands of individuals using social media to discuss health concerns, sensitive personal data is self-disclosed on these platforms every day. Previous research indicates an understanding of social privacy concerns by patients with chronic illnesses, but there is a lack of understanding in the perception of information privacy concerns. Qualitative interviews were conducted with 38 patients with inflammatory bowel disease (IBD) using social media platforms to engage with online communities. Using thematic analysis, we identified that patients typically demonstrate the privacy and risk dual calculus for perceived social privacy concerns. Patients demonstrate mixed knowledge of what data is collected and how it is used by social media platforms and often described their platform use as a trade-off between the unknown information privacy risks and the therapeutic affordances of engaging with the online community (the privacy calculus). Our findings illustrate the different levels of understanding between social and information privacy and the impacts on how individuals take agency over their personal data. We conclude with the suggestion for future research to further understand the relationship between knowledge, information privacy concerns and mitigating actions in the online health community context.

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