Quality of Life and Relationships in Caregivers of People With Dementia. A Gender Perspective

Author:

Bjørge Heidi1ORCID,Kvaal Kari2,Ulstein Ingun3

Affiliation:

1. OsloMet – Oslo Metropolitan University, Faculty of Health, Institute of Nursing and Health Promotion, Oslo, Norway

2. Inland Norway University of Applied Sciences, Faculty of Health and Social Sciences, Elverum, Norway

3. The Memory Clinic, Department of Geriatric Medicine, Oslo University Hospital Trust, Oslo, Norway

Abstract

Home-dwelling people with dementia rely on their family members to be able to stay at home. This affects the family caregivers’ quality of life (QoL). However, less is known about how male and female caregivers differ in their QoL. Our study aimed to investigate gender differences in caregivers’ quality of life (QoL), whether emotional relationships influence QoL, and how their QoL changes over time. The study applied a cross-sectional and a longitudinal design to examine a total of 208 caregivers, 158 female and 50 male caregivers, and their family member with dementia. Regression analysis and t-tests were performed to identify what characteristics about caregivers and care receivers influence male and female QoL, and whether caregivers’ QoL developed after one year. Both male and female caregivers’ depression influenced their QoL. For females, their own social distress influenced their QoL, and for males, their experience of their care receivers’ overemotional attitude influenced their QoL. From baseline to one-year follow-up their QoL decreased while their distress and experience of care receivers’ emotional attitudes was stable. Significant gender-specific differences were found, indicating that gender must be considered when approving caregivers’ needs and planning interventions for caregivers.

Publisher

SAGE Publications

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