Astrid Pozet, Sophie Darnis, Magalie Bonnet, Aurélia Meurisse, Tienhan Sandrine Dabakuyo-Yonli, Catherine Lejeune, Philippe Fagnoni, Maryse Gaimard, Patrick Manckoundia, Clémence Quibel, Mélanie Marchand, Amélie Anota, Virginie Nerich
Journal: International journal of public health 2023;68():1605459
PMID: 37711159
Nearly 25% of employed individuals in European countries are expected to take on unpaid caregiving responsibilities, assisting elderly people. Caregiving responsibilities are extremely demanding and can impact various aspects of life, including mental and physical health and overall well-being. Monitoring caregiver mental health and providing support through respite care, education, and long-term care can alleviate caregiving burdens and prevent deterioration. This multicenter, open-label, randomised study assessed caregiver Quality of Life (QoL), anxiety, depression, and burden at one and two years, who received an information booklet and social worker support or information booklet exclusively. Healthcare professionals can use the information from this study to gain insight into caregivers' needs and the beneficial effects of social support in mitigating depression. Further robust studies are required to identify caregivers' needs and the types of support necessary to address their issues and help them efficiently.
To assess health-related quality of life (QoL) in caregivers of elderly patients with chronic disabilities receiving, or not receiving, social worker support. This multicenter open-label randomized study assigned caregivers to receive an information booklet, exclusively, or with social worker support. Caregivers completed Short Form-36 (SF-36) and Hospital Anxiety Depression Scale quarterly, and Zarit Burden Interview each semester, for 24 months. We reported caregiver QoL mean changes at 12 and 24 months (M12, M24). Longitudinal QoL analysis up to M24 used mixed models for repeated measures (MMRM). Among the 179 caregivers randomized from 2015 to 2019, the SF-36 physical and mental component summary showed no significant changes at M12 and M24, in terms of neither anxiety nor burden. However, depression significantly increased (M12: 1.4 ± 4.0; M24: 1.7 ± 4.1) with significant adjusted mean increase using MMRM at M24: 3.4 [0.6-2.5] in the control group, exclusively. These findings call for better recognition of the social support to prevent caregiver QoL deterioration and alleviate their depression early in the course of the disease. ClinicalTrials.gov, identifier NCT02626377.
Copyright © 2023 Pozet, Darnis, Bonnet, Meurisse, Dabakuyo-Yonli, Lejeune, Fagnoni, Gaimard, Manckoundia, Quibel, Marchand, Anota and Nerich.
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