Chatting: Family carers' perspectives on receiving support from dementia crisis teams
| dc.contributor.author | Dening, Tom | |
| dc.date.accessioned | 2024-07-23T13:10:56Z | |
| dc.date.available | 2024-07-23T13:10:56Z | |
| dc.date.issued | 2024 | |
| dc.identifier.citation | Redley, M., Poland, F., Hoe, J., Dening, T., Stanyon, M., Yates, J., Streater, A., Coleston-Shields, D. & Orrell, M. (2024). Chatting: Family carers' perspectives on receiving support from dementia crisis teams. Healthcare, 12 (11). | en_US |
| dc.identifier.other | 10.3390/healthcare12111122 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.12904/18844 | |
| dc.description | © 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/) | |
| dc.description.abstract | Family caregivers are vital to enabling people with dementia to live longer in their own homes. For these caregivers, chatting with clinicians-being listened to empathetically and receiving reassurance-can be seen as not incidental but important to supporting them. This paper considers and identifies the significance of this relational work for family carers by re-examining data originally collected to document caregivers' perspectives on quality in crisis response teams. This reveals that chatting, for family caregivers, comprises three related features: (i) that family caregivers by responding to a person's changing and sometimes challenging needs and behaviors inhabit a precarious equilibrium; (ii) that caregivers greatly appreciate 'chatting' with visiting clinicians; and (iii) that while caregivers appreciate these chats, they can be highly critical of the institutionalized character of a crisis response team's involvement with them. | |
| dc.description.uri | https://www.mdpi.com/2227-9032/12/11/1122 | en_US |
| dc.format | Full text uploaded | |
| dc.language.iso | en | en_US |
| dc.subject | Dementia | en_US |
| dc.subject | Carers | en_US |
| dc.title | Chatting: Family carers' perspectives on receiving support from dementia crisis teams | en_US |
| dc.type | Article | en_US |
| dcterms.dateAccepted | 2024-05-30 | |
| rioxxterms.funder | Default funder | en_US |
| rioxxterms.identifier.project | Default project | en_US |
| rioxxterms.version | NA | en_US |
| rioxxterms.licenseref.startdate | 2024 | |
| rioxxterms.type | Journal Article/Review | en_US |
| refterms.dateFOA | 2024-07-23T13:10:58Z | |
| refterms.panel | Unspecified | en_US |
| refterms.dateFirstOnline | 2024-05-30 | |
| html.description.abstract | Family caregivers are vital to enabling people with dementia to live longer in their own homes. For these caregivers, chatting with clinicians-being listened to empathetically and receiving reassurance-can be seen as not incidental but important to supporting them. This paper considers and identifies the significance of this relational work for family carers by re-examining data originally collected to document caregivers' perspectives on quality in crisis response teams. This reveals that chatting, for family caregivers, comprises three related features: (i) that family caregivers by responding to a person's changing and sometimes challenging needs and behaviors inhabit a precarious equilibrium; (ii) that caregivers greatly appreciate 'chatting' with visiting clinicians; and (iii) that while caregivers appreciate these chats, they can be highly critical of the institutionalized character of a crisis response team's involvement with them. | en_US |
| rioxxterms.funder.project | 94a427429a5bcfef7dd04c33360d80cd | en_US |
