Essay sample library > Quantitative Study: Burdens among Parkinson’s disease Caregiver

Quantitative Study: Burdens among Parkinson’s disease Caregiver

2024-01-03 01:57:55

Introduction "Parkinson's disease is usually life threatening It is described as a progressive disease of chronic, nervous system is the second most common neurological disease after Alzheimer's disease, but can not be cured ( Magennis & Collie, 2013) Although it is not an antidote for Parkinson's disease, PD gradually helps patients who can not meet their daily needs, when PD gradually began to affect cognitive motor, and emotional function Because we need nursing staff to help, we need to help caregivers.

I am a candidate for doctoral course at the University of Tennessee social work school. I will restore research research on the burden of Alzheimer's disease patients and carers. I would like to use the caregiver burden list as an indicator of the burden of the caregiver. Thanks for your cooperation. I am waiting for your reply. I'm sorry to postpone the license. Please do your best. ************************************************** ***************** Dr. Lindatelli Northwest Research Group Regional Health Department Psychosocial and Regional Health Professor and Director, Nursing School, Director of Washington University of the Elderly: 358733 Seattle, WA 98195 telephone: 206-543-0715 FAX number: 206-616-5588

Recommended quotation Scott, Cathy B, "Burden of Caregiver of Alzheimer's Disease: Function to Restore Important It", Ph.D University of Tennessee, 2010.https: //trace.tennessee.edu/utk_graddiss/912

Elmstnhl S (2008) conducted a cross-sectional study to evaluate caregivers of economic burden and dementia patients Sweden's psychological distress. 50 nursing staff participated. A burdensome questionnaire is used to evaluate economic and social situations. In the research, I showed the burden of the cause caregiver to the total experience, the feeling of tension and the burden of low-income people connecting to higher degree of despair. Hauke ​​WW (2011) conducted a prospective study to evaluate the tailor-made program of activities to alleviate the burden on caregivers of dementia patients. 60 nursing staff participated. In order to reduce the burden on caregivers, an activity plan coordinated as an intervention for 4 months was offered. The interview schedule of Zarit Burden is used to evaluate the degree of burden. According to research results, the individual activity program alleviates depression and anxiety among caregivers of dementia patients