Abstract
ABSTRACT Caregivers’ burden may vary across different countries. The aim of this study was to evaluate factors associated with caregivers’ burden in a sample of Greek patient-caregiver dyads, including patients’ frailty status among the evaluated variables. In 204 patient-caregiver dyads, patients’ and caregivers’ characteristics were recorded. Caregiver burden was evaluated by using the Zarit Burden Interview, and patients’ frailty status by using Clinical Frailty Scale (CFS). Parametric and non-parametric tests and logistic regression analysis were applied to identify the factors that had a significant association with caregivers’ burden. Increasing CFS score (p = .001, OR = 1.467, 95%CI 1.178–1.826) and longer duration of caregiving (p = .003, OR = 1.017, 95%CI 1.006–1.028) were associated with an increased likelihood of caregivers’ burden. Patients’ frailty status is probably a modifiable factor among them that has an impact on caregivers’ burden. Strategies and interventions in order to prevent, delay or reverse frailty may have a positive impact on reducing this burden.
Published Version
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