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Informal care burden during the COVID‐19 pandemic in Flanders, Belgium: The role of perceived threat, personality and resilience.
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- Author(s): De Coninck, David; Van Doren, Shauni; Matthijs, Koen; Declercq, Anja
- Source:
Scandinavian Journal of Caring Sciences. Jun2023, Vol. 37 Issue 2, p350-363. 14p. 5 Charts. - Source:
- Additional Information
- Subject Terms: COMPETENCY assessment (Law); PSYCHOLOGICAL resilience; RISK assessment; T-test (Statistics); LOGISTIC regression analysis; EMPIRICAL research; HUMANITY; PATIENT care; DESCRIPTIVE statistics; BURDEN of care; LONGITUDINAL method; SURVEYS; PERSONALITY; PSYCHOLOGICAL stress; ANALYSIS of variance; PSYCHOLOGY of caregivers; SOCIODEMOGRAPHIC factors; PUBLIC administration; MEDICAL needs assessment; COMPARATIVE studies; COVID-19 pandemic; COVID-19; SOCIAL participation; WELL-being; PSYCHOSOCIAL factors
- Subject Terms:
- Abstract: Background: In this study, we investigate how socio‐demographic characteristics (age, gender and education) and informal care relationship characteristics (e.g., time spent on care, number of informal caregivers, professional care) are linked with informal care burden during the COVID‐19 pandemic. In addition, we expect this burden to differ by personality characteristics, degree of resilience, and—in this specific context—perceived the COVID‐19 threat. Method: We used the fifth wave of a longitudinal study to identify 258 informal caregivers. These online survey data came from a five‐wave longitudinal study in Flanders, Belgium that ran from April 2020 to April 2021. Data were representative of the adult population by age and gender. Analyses include t‐tests, ANOVA, SEM and binomial logistic regression. Results: We found that the informal care burden was strongly linked with a socio‐economic gradient, time investment changes in care since the start of the pandemic, and whether there was more than one informal caregiver. Personality traits such as agreeableness and openness to experience, and the perceived threat of COVID‐19 were also related to care burden. Conclusions: During the pandemic, informal caregivers were put under extra considerable pressure: restrictive government measures sometimes led to the temporary suspension of some or all professional care for persons with care needs, which may have resulted in a growing psychosocial burden. We recommend that, in the future, the focus should be on supporting the mental wellbeing and social participation of caregivers along with measures to protect caregivers and their relatives from COVID‐19. Support structures for informal caregivers should be kept running during crises now and in the future, but it is also important to adopt a case‐by‐case basis to consider support for informal caregivers. [ABSTRACT FROM AUTHOR]
- Abstract: Copyright of Scandinavian Journal of Caring Sciences is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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