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Lookup NU author(s): Dr Matthias WienrothORCiD
This is the authors' accepted manuscript of an article that has been published in its final definitive form by Wiley-Blackwell, 2019.
For re-use rights please refer to the publisher's terms and conditions.
The National Institute for Health Research (NIHR) aims to improve national “health and wealth” by providing infrastructural support to enable clinical research in National Health Service (NHS) settings in England and Wales. Cognisant of the consequences of studies’ failure to achieve required numbers of participants, it also actively campaigns to promote patient awareness of research, and willingness to participate in trials. In this paper we analyse recent NIHR campaigns and policies designed to encourage patients to participate in clinical research to interrogate how they are implicated in the national bioeconomy. In doing so we expand the notion of ‘clinical labour’ to include the work of patient recruitment and highlight an emergent obligation on patients to contribute to research processes. Whereas once patient knowledge and experience may have been devalued, here we draw on the concept of ‘assetization’ (Birch 2017) to explore the emergent relationship between healthcare system and patient as research participant. We consider how patients’ contribution goes beyond the provision of standardised objects of valuation so that patients themselves may be perceived as assets to, not only recipients of, the national healthcare system.
Author(s): Wienroth M, Pearce C, McKevitt C
Publication type: Article
Publication status: Published
Journal: Sociology of Health and Illness
Year: 2019
Volume: 41
Issue: 7
Pages: 1444-1461
Print publication date: 01/09/2019
Online publication date: 22/05/2019
Acceptance date: 29/04/2019
Date deposited: 30/04/2019
ISSN (print): 0141-9889
ISSN (electronic): 1467-9566
Publisher: Wiley-Blackwell
URL: https://doi.org/10.1111/1467-9566.12957
DOI: 10.1111/1467-9566.12957
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