scholarly journals The Social Networks of Hong Kong Chinese Family Caregivers of Alzheimer's Disease: Correlates With Positive Gains and Burden

2013 ◽  
Vol 53 (6) ◽  
pp. 998-1008 ◽  
Author(s):  
S.-T. Cheng ◽  
L. C. W. Lam ◽  
T. Kwok ◽  
N. S. S. Ng ◽  
A. W. T. Fung
2020 ◽  
Vol 16 (S3) ◽  
Author(s):  
Xiaopu Zhou ◽  
Yu Chen ◽  
Nicole Chit Hang Lai ◽  
Yuen Tung Li ◽  
Timothy C.Y. Kwok ◽  
...  

2018 ◽  
Vol 68 ◽  
pp. 160.e1-160.e7 ◽  
Author(s):  
Binbin Wang ◽  
Suying Bao ◽  
Zhigang Zhang ◽  
Xueya Zhou ◽  
Jing Wang ◽  
...  

2016 ◽  
Vol 50 (1) ◽  
pp. 79-85 ◽  
Author(s):  
Aline Duarte Folle ◽  
Helena Eri Shimizu ◽  
Janeth de Oliveira Silva Naves

Abstract OBJECTIVE To understand the content of Social Representation (SR) of family caregivers of Alzheimer's disease patients. METHOD Interviews were conducted with 26 caregivers and analyzed by the ALCESTE software. RESULTS The SR content was structured in two thematic axes called Daily Life and Care and Medical and Emotional Concepts and Outcomes. The first axis creates images related to the routine of interaction with the sick person, and contains a description of care procedures, experiences, and practices applied every day. The second is composed of subjective and conceptual aspects that make up the social representation of Alzheimer's disease, with meanings related to the emotional, medical, and biological contexts. CONCLUSION Due to the importance of topics related to patients' dependence and the personal and emotional consequences of the disease, overload is the main content of the SR of Alzheimer's disease for caregivers, and the understanding of these SR by health professionals should support the planning of interventions addressing this group of individuals.


2021 ◽  
pp. 1-13
Author(s):  
Shuying Zhang ◽  
Jianing Qi ◽  
Qing Yang ◽  
Qihao Guo

ABSTRACT Objectives: To examine the psychometric properties of the Chinese version of the Relevant Outcome Scale for Alzheimer’s disease (CROSA) among persons with AD (PWAD) and their caregivers in China. Design: A single-arm, open-label, multi-center study. Setting: Two tertiary general hospitals in Shanghai. Participants: A total of 336 PWAD and their family caregivers. Intervention: The PWAD completed a 12-week treatment with memantine after a baseline assessment. Measurements: The CROSA and the Chinese versions of the Mini-Mental State Examination, the Alzheimer’s Disease Assessment Scale-Cognitive Subscale, the Disability Activity of Dementia, the Neuropsychiatric Inventory Questionnaire, the Zarit Caregiver Burden Interview and the Self-Efficacy Questionnaire for Chinese Family Caregivers. Results: The Cronbach’s alpha for the total scale was 0.900, and the intraclass correlation coefficient and Pearson’s correlation coefficient were 0.910 (P < 0.001) and 0.836 (P < 0.001), respectively. Confirmatory factor analysis revealed the two-factor model to be consistent with the original version. For the known-group validity, the total score of the CROSA classified the PWAD into three stages and three MMSE score groups. Moderate to large correlations with the validated scales confirmed the criteria validity of the CROSA, and the convergent validity was confirmed via testing a hypothesized caregiving model; however, only minimal responsiveness was found among the deterioration group after 12 weeks of treatment with memantine. Conclusions: The reliability and validity of the CROSA was good or acceptable for use in daily clinical settings. Further studies are needed to examine the psychometric properties of the scale.


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