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[article]
Titre : |
Developments in public involvement and co-production in research: Embracing our values and those of our service users and carers |
Type de document : |
texte imprimé |
Auteurs : |
Priscilla Harries ; Duncan Barron ; Claire Ballinger |
Année de publication : |
2020 |
Article en page(s) : |
p. 3-5 |
Note générale : |
doi.org/10.1177/0308022619844143 |
Langues : |
Anglais (eng) |
Résumé : |
Public involvement (PI) (also known as patient and public involvement or PPI) refers to professionals and the public working together as equal partners, to ensure high quality research and service provision; it is also sometimes referred to as service user and carer involvement (Pandya-Wood et al., 2019). Many countries began to involve people in health issues following the World Health Organization declaration of Alma-Ata of 1978, which stated that ‘people have the rights and the duty to participate individually and collectively in their health care’ (World Health Organization, 1978: 1). The Rome Declaration on Responsible Research and Innovation (RRI) in Europe (2014) called on all stakeholders to work together, for example, to define research agendas and in the conduct and dissemination of research. The RRI concludes that excellence in research includes ‘openness, responsibility and the co-production of knowledge’ (RRI, 2014: 1). |
En ligne : |
https://journals.sagepub.com/doi/epub/10.1177/0308022619844143 |
Permalink : |
./index.php?lvl=notice_display&id=85689 |
in The British Journal of Occupational Therapy > Vol. 83 Issue 1 (Janvier 2020) . - p. 3-5
[article] Developments in public involvement and co-production in research: Embracing our values and those of our service users and carers [texte imprimé] / Priscilla Harries ; Duncan Barron ; Claire Ballinger . - 2020 . - p. 3-5. doi.org/10.1177/0308022619844143 Langues : Anglais ( eng) in The British Journal of Occupational Therapy > Vol. 83 Issue 1 (Janvier 2020) . - p. 3-5
Résumé : |
Public involvement (PI) (also known as patient and public involvement or PPI) refers to professionals and the public working together as equal partners, to ensure high quality research and service provision; it is also sometimes referred to as service user and carer involvement (Pandya-Wood et al., 2019). Many countries began to involve people in health issues following the World Health Organization declaration of Alma-Ata of 1978, which stated that ‘people have the rights and the duty to participate individually and collectively in their health care’ (World Health Organization, 1978: 1). The Rome Declaration on Responsible Research and Innovation (RRI) in Europe (2014) called on all stakeholders to work together, for example, to define research agendas and in the conduct and dissemination of research. The RRI concludes that excellence in research includes ‘openness, responsibility and the co-production of knowledge’ (RRI, 2014: 1). |
En ligne : |
https://journals.sagepub.com/doi/epub/10.1177/0308022619844143 |
Permalink : |
./index.php?lvl=notice_display&id=85689 |
| ![Developments in public involvement and co-production in research: Embracing our values and those of our service users and carers vignette](./getimage.php?url_image=http%3A%2F%2Fimages-eu.amazon.com%2Fimages%2FP%2F%21%21isbn%21%21.08.MZZZZZZZ.jpg¬icecode=&vigurl=https%3A%2F%2Fuk.sagepub.com%2Fsites%2Fdefault%2Ffiles%2Fupm-binaries%2Fstyles%2Fsage_thumbnail_width_150px%2Ffeed%2F110126_spbjo_83_3_72ppiRGB_150pixw.jpg) |
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