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  • McCosker, Anthony  (2)
  • 1
    Online Resource
    Online Resource
    SAGE Publications ; 2022
    In:  Big Data & Society Vol. 9, No. 1 ( 2022-01), p. 205395172210998-
    In: Big Data & Society, SAGE Publications, Vol. 9, No. 1 ( 2022-01), p. 205395172210998-
    Abstract: In this paper, we explore the methodologies underpinning two participatory research collaborations with Australian non-profit organisations that aimed to build data capability and social benefit in data use. We suggest that studying and intervening in data practices in situ, that is, in organisational data settings expands opportunities for improving the social value of data. These situated and collaborative approaches not only address the ‘expertise lag’ for non-profits but also help to realign the potential social value of organisational data use. We explore the relationship between data literacy, data expertise and data capability to test the idea that collaborative work with non-profit organisations can be a practical step towards addressing data equity and generating data-driven social outcomes. Rather than adopting approaches to data literacy that focus on individuals – or ideal ‘data citizens’ – we target the organisation-wide data settings, goals and practices of the non-profit sector. We conclude that participatory methods can embed social value-generating data capability where it can be sustained at an organisational level, aligning with community needs to promote collaborative data action.
    Type of Medium: Online Resource
    ISSN: 2053-9517 , 2053-9517
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2022
    detail.hit.zdb_id: 2773948-X
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  • 2
    Online Resource
    Online Resource
    University of Illinois Libraries ; 2020
    In:  AoIR Selected Papers of Internet Research ( 2020-10-05)
    In: AoIR Selected Papers of Internet Research, University of Illinois Libraries, ( 2020-10-05)
    Abstract: Practices of self-care and social support have long been identified across social media platforms and apps, as people find new ways of using and adapting digital technologies to mediate and address personal and public health issues. But digital health participation is considerably contested and unevenly experienced, whether through the commodified ‘platformization’ of the health sector, or in the potentially ‘unhealthy’ engagement with dominant social media platforms or dating and hookup apps. Contemporary policy frameworks for participatory, digital-enabled healthcare (e.g., NHS, 2019) assume that we all engage in health or help seeking practices online, but have no answers to associated risks of over-exposure, invasive health surveillance or experiences of discrimination and harassment online, particularly for those at the margins. In our case studies, this is pertinent for transgender, non-binary and female hookup app users, people seeking support for mental ill-health, illicit drug users participating in crypto-markets and dark web communities. In response to this scenario, this panel asks: what are the forms and capacities for collective care in the current digital ecosystem, between social media platforms and dating apps struggling to address harassment or mental wellbeing, within health service-supported online forums, and across the dark web? This panel looks at evidence and answers, as well as research practices and ethics, to understand personal and collective attempts to negotiate, manage, circumvent and otherwise find ways to reinvent cultures of care through digital platforms.
    Type of Medium: Online Resource
    ISSN: 2162-3317 , 2162-3317
    Language: Unknown
    Publisher: University of Illinois Libraries
    Publication Date: 2020
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