Abstract
The burden on the caregiver patients with Alzheimer disease need assistance and supervision in their daily activities. In literature, the term “burden” has been used to indicate the overload of work experienced by the caregiver. In our country, the patient’s domiciliary “take-care system” is based firstly on the family support together with the supply of health care providers and home care professionals provided by the National Health System. Caregivers of Alzheimer’s Disease (AD) patients are usually subjected to enormous physical and mental stress, as well as emotional, which may have repercussions on personal, familiar and social contest and, consequently, on life’s quality [1]. The aim of our study was to investigate caregiver’s burden “predicting factors” and evaluates to improve the quality of their caregivers.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
