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http://hdl.handle.net/2445/171774
Title: | Caregivers' Sense of Coherence: Implications on Direct and Indirect Costs of Dementia Care |
Author: | Turró-Garriga, Oriol Viñas Díez, Vanesa Conde Sala, Josep Lluís Calvó Perxas, Laia Cullell Juncà, Marta Mas-Vall-LLosera, Glòria Flaqué, Margarida Turon Estrada, Antoni Juvinyà Canal, Dolors Mioshi, Eneida Garre Olmo, Josep |
Keywords: | Malaltia d'Alzheimer Cuidadors Demència Alzheimer's disease Caregivers Dementia |
Issue Date: | 8-Sep-2020 |
Publisher: | IOS Press |
Abstract: | Background: Dementia care is associated with physical, emotional, and monetary impact on the informal carers providing unpaid care. Differences in the personal characteristics of caregivers may help explain the variations in the costs of dementia care. Objective: The aim of this study was to analyze the effect of caregivers' sense of coherence (SOC) on direct and indirect costs in dementia care. Methods: A cross-sectional study was conducted in community dwelling caregivers of patients with Alzheimer's disease. Data of healthcare services were obtained from clinical registries, and information was collected from caregivers regarding their use of social care resources and time spent caregiving. The transformation of all costs into Euros was made assigning a fixed cost of 10.29 ¿ /h and 16.24 ¿ /h for assisting in instrumental and basic activities of daily living, respectively. Caregivers' SOC was assessed using the Orientation to Life Questionnaire (OLQ-13). Adjusted regression models were developed, with different types of costs as dependent variables. Results: A sample of 147 caregivers was recruited. The mean OLQ-13 score was 73.3 points (SD = 11.6). The regression models showed a small association between caregivers' SOC and direct costs, mainly linked to the use of social care resources (r2 = 0.429; β= -15.6 ¿ /month), and a greater association between SOC and indirect costs (r2 = 0.562; β= -222.3 ¿ /month). Conclusion: Increasing caregivers' SOC could reduce dementia care costs by decreasing the use of social care resources and caregiving time. |
Note: | Reproducció del document publicat a: https://doi.org/10.3233/JAD-200350 |
It is part of: | Journal of Alzheimer's Disease, 2020, vol. 78, num. 1, p. 117-126 |
URI: | http://hdl.handle.net/2445/171774 |
Related resource: | https://doi.org/10.3233/JAD-200350 |
ISSN: | 1387-2877 |
Appears in Collections: | Articles publicats en revistes (Cognició, Desenvolupament i Psicologia de l'Educació) |
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