scholarly journals Factors Influencing the Quality of Life among Family Caregivers of the Elderly with Dementia

2021 ◽  
Vol 28 (4) ◽  
pp. 500-509
Author(s):  
Hwasoon Kim

Purpose: The purpose of this study was to identify quality of life of family caregivers and to investigate factors positively and negatively affecting family caregivers’ quality of life.Methods: Participants were 153 family caregivers taking care of dementia elderly. Collected data were general characteristics, quality of life, care burden, depression, social support, family relationship, and problematic behaviors. Data were analyzed using descriptive statistics, independent t-tests, Pearson correlation coefficient, and multiple regression.Results: Mean age of participants was 58.70±13.88. The average scores of main variables for family relationship, social support, quality of life, care burden, problematic behaviors and depression were 3.99±1.08, 3.34±0.84, 3.00±0.63, 1.96±0.51, 1.48±1.06, 1.17±0.71 and 1.13±0.61, respectively. In regression analysis, depression (β=-.20), subjective health (β=.26), social support (β=.23), education level (β=-.20), and care burden (β=-.22) accounted for 59.1% of the variance in quality of life.Conclusion: To increase quality of life for family caregivers, interventions should be focused on reducing depression and care burden, enhancing caregiver’s health and social support. especially for family caregivers who received lower education.

2014 ◽  
Vol 32 (7) ◽  
pp. 767-771 ◽  
Author(s):  
Patricia Dobríková ◽  
Dušana Pčolková ◽  
Layla Khalil AlTurabi ◽  
Daniel J. West

2003 ◽  
Vol 55 (2) ◽  
pp. 148-149
Author(s):  
N Iida ◽  
N Kohashi ◽  
T Okamura ◽  
K Nagao ◽  
J Jamshidi ◽  
...  

2017 ◽  
Vol 3 (1) ◽  
pp. 41 ◽  
Author(s):  
José Manuel Ponsoda Tornal ◽  
Amelia Díaz Martínez

The aim of this work is to determine the role that social support, coping, optimism, quality of life, resilience and life satisfaction have on the relationship between objective and subjective burden on family caregivers of Alzheimer patients. Method: Participants: 140 caregivers of Alzheimer patients. Instruments: Sociodemographic Data; CBI Caregiver Burden Scale; COPE Coping Styles Scale; DUKE.UNC Social Support Scale; LOT-R, Life Orientation TestRevised; QOLLTI-F, Quality of Life in Life Threatening Illness Scale–Family Carers Version; CD-RISC, Connor-Davidson Resilience Scale; SWLS, Satisfaction with Life Scale. Procedure: Implementation of scales in an individual, voluntary, anonymous way, including informed consent. Results: All variables studied produced significant differences between caregivers with high and low subjective burden, except time caring measured in months/years. Relationships between the variables were significant, with the exception of months/years caring and coping styles. Social support, optimism, satisfaction and quality of life have an important mediating role between objective and subjective burden. Conclusions and discussion: Social support, optimism, satisfaction and quality of life have been decisive as mediating variables between hours a day taking care (objective burden) and subjective burden. This result represents a step forward in the analysis and subsequent creation of intervention programs in family caregivers.


Sign in / Sign up

Export Citation Format

Share Document