The role of subjective social status in living well for carers of people with dementia: findings from the Improving the experience of Dementia and Enhancing Active Life programme

Victor, C; Rippon, I; Quinn, C; Martyr, A; Clare, L

Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/22142

Full metadata record

DC Field	Value	Language
dc.contributor.author	Victor, C	-
dc.contributor.author	Rippon, I	-
dc.contributor.author	Quinn, C	-
dc.contributor.author	Martyr, A	-
dc.contributor.author	Clare, L	-
dc.date.accessioned	2021-01-24T12:51:37Z	-
dc.date.available	2021-01-24T12:51:37Z	-
dc.date.issued	2021-02-08	-
dc.identifier.citation	Victor, C., Rippon, I., Quinn, C., Martyr, A. and Clare, L. (2021) 'The role of subjective social status in living well for carers of people with dementia: findings from the Improving the experience of Dementia and Enhancing Active Life programme', International Journal of Care and Caring, 5 (3), pp. 446-466. doi: 10.1332/239788221X16104266615749.	en_US
dc.identifier.issn	2397-8821	-
dc.identifier.uri	https://bura.brunel.ac.uk/handle/2438/22142	-
dc.description.sponsorship	‘Improving the experience of Dementia and Enhancing Active Life: living well with dementia. The IDEAL study’ was funded jointly by the Economic and Social Research Council (ESRC) and the National Institute for Health Research (NIHR) through grant ES/L001853/2. Investigators: L. Clare, I.R. Jones, C. Victor, J.V. Hindle, R.W. Jones, M. Knapp, M. Kopelman, R. Litherland, A. Martyr, F. Matthews, R.G. Morris, S.M. Nelis, J. Pickett, C. Quinn, J. Rusted, J. Thom. ESRC is part of UK Research and Innovation (UKRI). ‘Improving the experience of Dementia and Enhancing Active Life: a longitudinal perspective on living well with dementia. The IDEAL-2 study’ is funded by Alzheimer’s Society, grant number 348, AS-PR2-16-001. Investigators: L. Clare, I.R. Jones, C. Victor, C. Ballard, A. Hillman, J.V. Hindle, J. Hughes, R.W. Jones, M. Knapp, R. Litherland, A. Martyr, F. Matthews, R.G. Morris, S.M. Nelis, C. Quinn, J. Rusted. The views expressed are those of the author(s) and not necessarily those of the ESRC, UKRI, NIHR, the Department of Health and Social Care, the National Health Service, or Alzheimer’s Society. The support of ESRC, NIHR and Alzheimer’s Society is gratefully acknowledged.	en_US
dc.format.extent	446 - 466 (21)	-
dc.language.iso	en	en_US
dc.publisher	Policy Press	en_US
dc.rights	This article is distributed under the terms of the Creative Commons Attribution 4.0 license (https://creativecommons.org/licenses/by/4.0/) which permits adaptation, alteration, reproduction and distribution without further permission provided the original work is attributed. The derivative works do not need to be licensed on the same terms.	-
dc.rights.uri	https://creativecommons.org/licenses/by/4.0/	-
dc.subject	informal caring	en_US
dc.subject	subjective social status	en_US
dc.subject	quality of life	en_US
dc.subject	well-being	en_US
dc.subject	life satisfaction	en_US
dc.title	The role of subjective social status in living well for carers of people with dementia: findings from the Improving the experience of Dementia and Enhancing Active Life programme	en_US
dc.title.alternative	The role of subjective social status in living well for carers of people with dementia: findings from the IDEAL programme	-
dc.type	Article	en_US
dc.identifier.doi	https://doi.org/10.1332/239788221X16104266615749	-
dc.relation.isPartOf	International Journal of Care and Caring	-
pubs.issue	3	-
pubs.publication-status	Published	-
pubs.volume	5	-
dc.identifier.eissn	2397-883X	-
Appears in Collections:	Dept of Health Sciences Research Papers

Files in This Item:

File	Description	Size	Format
FullText.pdf		848.29 kB	Adobe PDF	View/Open

Show simple item record

This item is licensed under a Creative Commons License