Vis enkel innførsel

dc.contributor.authorHäikiö, Kristin
dc.contributor.authorSagbakken, Mette
dc.contributor.authorRugkåsa, Jorun
dc.date.accessioned2021-04-08T09:22:00Z
dc.date.available2021-04-08T09:22:00Z
dc.date.created2020-08-18T12:03:39Z
dc.date.issued2020
dc.identifier.citationHäikiö, K., Sagbakken, M. & Rugkåsa, J. (2020). Family carers’ involvement strategies in response to sub-optimal health services to older adults living with dementia – a qualitative study. BMC Geriatrics, 20, 290.en_US
dc.identifier.issn1471-2318
dc.identifier.urihttps://hdl.handle.net/11250/2736810
dc.description.abstractBackground: While dementia policy strategies emphasize the importance of partnerships between families and formal carers to provide tailored care and effectively allocate community resources, family carers often feel left out or excluded. Poor communication has been identified as one reason for the lack of good partnerships. Few studies have investigated how family carers seek to involve themselves when they experience sub-optimal services, and how their strategies may depend on different considerations and personal abilities. Methods: Qualitative in-depth interviews were conducted with 23 family carers to explore their experiences with, perspectives on, contributions to, and interactions with healthcare services provided to older adults living with dementia. To capture nuances and variations, a semi-structured interview guide was used. Interviews were audio-recorded and transcribed verbatim. A four-step analysis of the transcripts was conducted, informed by hermeneutic and phenomenological methodology. Results: Two main involvement strategies were identified: 1) being “the hub in the wheel” and 2) getting the wheel rolling. The first strategy was used to support and complement health services, while the second was used to add momentum and leverage to arguments or processes. The two main strategies were used differently among participants, in part due to differences in personal resources and the ability to utilize these, but also in light of family carers’ weighing conflicting concerns and perceived costs and benefits. Conclusions: Awareness and acknowledgment of family carers’ strategies, personal resources, and considerations may help policymakers and healthcare personnel when they build or maintain good partnerships together with family carers. A better understanding of family carers’ own perspectives on carer involvement is a necessary precursor to developing good care partnerships.en_US
dc.language.isoengen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleFamily carers’ involvement strategies in response to sub-optimal health services to older adults living with dementia – a qualitative studyen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© The Author(s), 2020.en_US
dc.source.volume20en_US
dc.source.journalBMC Geriatricsen_US
dc.identifier.doihttps://doi.org/10.1186/s12877-020-01663-z
dc.identifier.cristin1823801
dc.relation.projectNorges forskningsråd: 256431en_US
dc.source.articlenumber290en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


Tilhørende fil(er)

Thumbnail

Denne innførselen finnes i følgende samling(er)

Vis enkel innførsel

Navngivelse 4.0 Internasjonal
Med mindre annet er angitt, så er denne innførselen lisensiert som Navngivelse 4.0 Internasjonal