The Burden of Next-of-Kin Carers of Dementia Sufferers in the Home Environment

The 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...

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Bibliographic Details
Published in:Healthcare (Basel) 2022-12, Vol.10 (12), p.2441
Main Authors: Tokovska, Miroslava, Šolcová, Jana
Format: Article
Language:English
Subjects:
Alzheimer's disease
Care and treatment
Caregivers
carers’ stress
Dementia
dementia sufferers
Domestic relations
Home environment
Long term health care
next-of-kin
Older people
Quality of life
Questionnaires
relative stress scale
Slovakia
Social support
Society
Stress
Support groups
Surveys
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Summary:The 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 ( = 0.001), social stress ( = 0.003), and negative feelings ( = 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.
ISSN:2227-9032
2227-9032
DOI:10.3390/healthcare10122441