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Health-Related Quality of Life and Caregiver’S Burden in Patients With Chronic Diseases: A Cross-Sectional Study Publisher



Mirhosseini S1 ; Bazghaleh M2 ; Basirinezhad MH3 ; Abbasi A2 ; Ebrahimi H4
Authors
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Authors Affiliations
  1. 1. Student Research Committee, School of Nursing and Midwifery, Mashhad University of Medical Sciences, Mashhad, Iran
  2. 2. Department of Nursing, School of Nursing and Midwifery, Shahroud University of Medical Sciences, Shahroud, Iran
  3. 3. Department of Epidemiology and Biostatistics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Center for Health Related Social and Behavioral Sciences Research, Shahroud University of Medical Sciences, Shahroud, Iran

Source: Family Medicine and Primary Care Review Published:2021


Abstract

Background. Cancer and type 2 diabetes (T2D), as two groups of prevalent chronic diseases, are associated with different social, economic and emotional consequences, and they can change the quality of life (QoL) of their caregivers. Objectives. The aim of the present study was to determine the relationship between QoL and the burden on caregivers of patients with cancer and T2D. Material and methods. This comparative cross-sectional study was conducted on 308 caregivers of patients with cancer and T2D. Data collection tools included a demographic characteristics form, SF-36 quality of life form and care burden inventory (Novak and Guest). Data was collected using the convenience sampling method. Data analysis was then carried out using descriptive and inferential statistics (linear backward stepwise regression method). Results. The mean age of the caregivers of patients with cancer and T2D was 41.30 ± 13.12 and 41.86 ± 12.78 years, respectively. There was no significant difference between the mean score of care burden and QoL in the two groups of caregivers. There was a significant direct relationship between caregivers’ QoL and caregivers' disease and a significant inverse relationship between caregivers’ education and caring burden. Conclusions. Caregivers of patients with chronic diseases suffer from care burden, which negatively affects their QoL; thus, it is recommended to reduce the care burden, increasing their QoL by providing appropriate mental, psychological, and social support. Due to the negative impact of caring burden on caregivers’ QoL, care services for chronic patients in developing countries should be strengthened. © by Wydawnictwo Continuo.
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