The power of symbolic capital in patient and public involvement in health research
Bibliographic Data
| ID | 19507435 |
|---|---|
| Authors | Louise Locock (0000-0002-8109-1930, Health Experiences Research Group Nuffield Department of Primary Care Health Sciences University of Oxford Oxford UK), Anne‐marie Boylan (0000-0001-8187-0742, Health Experiences Research Group Nuffield Department of Primary Care Health Sciences University of Oxford Oxford UK, corresponding author), Rosamund Snow (Health Experiences Research Group Nuffield Department of Primary Care Health Sciences University of Oxford Oxford UK), Sophie Staniszewska (0000-0002-7723-9074, WMS—Royal College of Nursing Research Institute University of Warwick Coventry UK) |
| Year | 2017 |
| Volume | 20 |
| Issue | 5 |
| Pages | 836-844 |
| Publication date | 2017-10-01 |
| Peer Reviewed | Yes |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | Health Expectations (JOURNAL) |
| Journal identifiers | ISSN: 1369-6513 • E-ISSN: 1369-7625 |
| Publisher | Wiley (PUBLISHER • GB) |
| DOI | 10.1111/hex.12519 |
| PMID | 27885770 |
| OpenAlex | W2550381095 |
| Language | EN |
| Citations received | 33 |
| References cited | 24 |
BACKGROUND: Policy-makers and health research funders increasingly require researchers to demonstrate that they have involved patients in the design and conduct of research. However, the extent to which patients and public have the power to get involved on an equal footing is dependent on their economic, cultural, social and symbolic capital. OBJECTIVE: To explore power relations in patient and public involvement (PPI) in research, particularly how patients may wield symbolic capital to develop a more equal relationship. METHODS: Narrative interviews with a maximum variation sample of 38 people involved as patients, carers or public in health research, analysed thematically. FINDINGS: Symbolic capital may be demonstrated in a range of ways (sometimes alongside or in the absence of other forms of capital): illness experience, technical illness knowledge and the challenging outsider. Symbolic capital is unstable and dependent on others for recognition and legitimacy. Nonetheless, participants identify a gradual shift in power relations over time. DISCUSSION AND CONCLUSIONS: Research into PPI has been conceptually and theoretically poor, limiting our understanding of its mechanisms and wider contextual elements. Our findings demonstrate the importance of reflecting on the forms of power and capital wielded by the health research community, and of acknowledging the way in which PPI is challenging the status quo. As one of the first papers to conceptualize how different forms of symbolic capital operate and their critical role in challenging the balance of power, our findings may help researchers better plan their PPI activities and reflect on their own power
Legitimacy · Narrative · Political science · Politics · Public relations · Social science · Sociology · Status quo · Symbolic capital · Symbolic power · The Symbolic · Mental Health and Patient Involvement · Participatory Visual Research Methods · Patient-Provider Communication in Healthcare · Psychology · Social Psychology
Involving Patients in Pharmacoepidemiology Studies Conducted on Healthcare Administrative Database
Bridging Lived and Expert Experience
Drawing straight lines along blurred boundaries
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Commercial influences on patient and public involvement
Exploring the hidden demands for patients’ resources
Reflections on engaging with an advisory network in the context of a ‘sensitive’ research study
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Symbolic Capital as a Resource of Promotion of Provincial Cities
From waste product to blood, brains and narratives
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Reciprocal relationships and the importance of feedback in patient and public involvement
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“About sixty per cent I want to do it”
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Meaningful patient and public involvement in digital health innovation, implementation and evaluation
Appropriating and asserting power on inflammatory arthritis teams
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Coming from two different worlds—A qualitative, exploratory study of the collaboration between patient representatives and researchers
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'A limpet on a ship'
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The rise of patient and public involvement in health research in Denmark – a qualitative study of funder's policies and practices
“An Active, Productive Life”
Conditions d'une démocratie en santé d'ordre maximaliste
A Reflection on Paradoxes and Double Binds in the Workplace in the Era of Super-Diversity
My full-time unpaid role
Power
Collecting data on patient experience is not enough
The co-dependency concept
Experience-based design
What ‘Patient-Centered’ Should Mean: Confessions Of An Extremist
Systematic review of involving patients in the planning and development of health care
Understanding Bourdieu
Mapping the impact of patient and public involvement on health and social care research
Weak and strong publics
The Logic of Practice
User Involvement in Research and Evaluation
Finding a way to pay in the UK
Coming Home
Publics, Patients, Citizens, Consumers? Power and Decision Making in Primary Health Care
Three-Dimensional Power
Justice interruptus
Theoretical directions for an emancipatory concept of patient and public involvement
| Unique citing works | 33 |
|---|---|
| Citations per year | 3,67 |
| Citation span | 2017 - 2026 (10) |
| Citation velocity | current |
| Highly cited | No |
| Citation types | Neutral: 29 |