Vis enkel innførsel

dc.contributor.authorTokovska, Miroslava
dc.contributor.authorŠolcová, Jana
dc.date.accessioned2023-03-01T12:21:16Z
dc.date.available2023-03-01T12:21:16Z
dc.date.created2022-12-04T07:50:51Z
dc.date.issued2022
dc.identifier.citationHealthcare 2022, 10(12), 2441.en_US
dc.identifier.issn2227-9032
dc.identifier.urihttps://hdl.handle.net/11250/3054976
dc.description.abstractThe role and responsibilities of next-of-kin carers are significant, filling several years of their lives and causing them to experience a burden of care. This study was conducted to investigate the burden of next-of-kin carers for dementia sufferers in Slovakia. Data were compiled via the Relatives’ Stress Scale (RSS) screening instrument through a survey of 112 primary next-of-kin carers and analysed using the statistical tests of descriptive statistics, means, scores and significance differences (Wilcoxon test). This is one of the few scales which provides: (a) specific measures of caregiver stress, and (b) is standardised for a population of informal carers in the home environment. The profiles of Slovak next-of-kin carers were identified with statistically significant characteristics (gender, age of carers). The study identified a high level of caregiving stress (82.15%), and selected factors were found to be significant in all burden dimensions: emotional stress (p = 0.001), social stress (p = 0.003), and negative feelings (p = 0.002). The results emphasise the need for coordination of healthcare and social services, possibly by expanding the network of social support groups, operating a counselling hotline/chat, and introducing national educational programmes for the next-of-kin carers of dementia sufferers. The results are also a source of reference for the umbrella organisation ‘the Slovak Alzheimer’s Society’ to access when implementing changes at a national level.en_US
dc.language.isoengen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectnext-of-kinen_US
dc.subjectpårørendeen_US
dc.subjectdementiaen_US
dc.subjectdemensen_US
dc.subjectburden of careen_US
dc.subjectomsorgsbelastningen_US
dc.titleThe Burden of Next-of-Kin Carers of Dementia Sufferers in the Home Environmenten_US
dc.title.alternativeThe Burden of Next-of-Kin Carers of Dementia Sufferers in the Home Environmenten_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.volume10en_US
dc.source.journalHealthcareen_US
dc.source.issue12en_US
dc.identifier.doi10.3390/healthcare10122441
dc.identifier.cristin2088227
dc.source.articlenumber2441en_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