Abstract
Alzheimer’s disease (AD) is a progressive neurodegenerative condition that not only impairs cognitive and functional abilities in patients but also imposes substantial psychosocial and emotional strain on their caregivers. This paper provides a comprehensive review of the psychosocial impact on relatives and caregivers, with a focus on caregiver burden, depressive symptoms, social isolation, and quality of life. In addition, an applied research component is presented, featuring a 6-week caregiver skills intervention program evaluated using the Zarit Burden Interview (ZBI) and the Center for Epidemiological Studies Depression Scale (CES-D). Results indicate significant reductions in caregiver burden and depressive symptoms post-intervention. Recommendations for policy, practice, and future research are also provided.
The author appreciates all those who participated in the study and helped to facilitate the research process.
The author declared no conflict of interest.
This is an Open Access Research distributed under the terms of the Creative Commons Attribution License (www.creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any Medium, provided the original work is properly cited.
© 2023, Patil, J.N.
Responding Author Information
Dr. Jayshri Nilkanth Patil @ Jayshri.patil@yahoo.com
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