98%
921
2 minutes
20
Background: Family caregivers are critical partners in the plan of care of people with disabilities. The study aims to demonstrate the factor structure and internal consistency of the Caregiver Burden Inventory (CBI) among the studied caregivers of disabled persons and to determine the effects of patients' and caregivers' characteristics on the burden and its dimensions.
Methods: A cross-sectional study among 260 family caregivers of disabled patients was carried out in a randomly chosen rural area, Minia, Egypt, 2019. Exploratory factor analysis (EFA) was conducted to determine the factorial validity of the CBI. Multiple linear regression was used to identify the significant factors affecting the burden.
Results: Factor analysis resulted in a five-factor solution using 20 items (four for each dimension) accounting for 72.7% of the total variance. The CBI and its dimensions showed high internal consistency (Cronbach's alpha value > 0.70). Education of caregiver, family income, mental impairments, and mixed disabilities were significant predictors of total CBI burden.
Conclusions: CBI is an effective multidimensional measure of the caregiver burden of disabled subjects. Caregivers experienced a distinct level of burden that is determined by caregiver and care recipient characteristics. Therefore, support and individualized counseling services should be optimized.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376710 | PMC |
http://dx.doi.org/10.1186/s12889-020-09266-4 | DOI Listing |
Dementia (London)
September 2025
International Observatory on End of Life Care, Lancaster University, UK.
As the prevalence of dementia rises exponentially globally, instituting practices to support the dying process of people affected by dementia is a public health priority. However, end-of-life quality indicators such as place of death provide limited information about the totality of the dying process. Hence, this study's aim was to identify factors affecting the relatively understudied concept of final place of care (where care was received in the last three days of life i.
View Article and Find Full Text PDFSleep Med Clin
September 2025
Department of Neurology, County Clinic Hospital, Calea Bucuresti 25-27 Street, 500037 Brasov; Faculty of Medicine, Transilvania University, Balcescu Street 56, 500040 Brasov, Romania.
Shifting away from the traditional perspective on parkisonism, which focused only on the motor state of the patients, recent research proves the importance of early recognition and treatment of non-motor symptoms. Patients with parkinsonism, who suffer from various sleep disturbances, such as excessive daytime sleepiness (EDS), experience lower quality of life, a negative impact on activities of daily living, and possible exposure to life-threatening situations. Implementing the routine use of subjective and objective means of diagnosing EDS, into clinical practice, allows for a personalised management plan, in scope of efficiently decreasing disease burden for both the patient and the caregiver.
View Article and Find Full Text PDFSleep Med Clin
September 2025
Department of Neurology, National Institute of Mental Health & Neuro Sciences (NIMHANS), Hosur Road, Bengaluru 560029, Karnataka, India. Electronic address:
Sleep dysfunction is a significant component of the non-motor symptom profile in Parkinson's disease (PD). Patients with early onset PD (EOPD) are a unique challenge and may present with specific patterns of sleep disturbances, which tend to be related to the underlying genetic causes. Furthermore, owing to the younger age of patients with EOPD, sleep disturbances significantly impact multiple domains including employment, ability to drive, social interactions, caregiver burden, and so forth.
View Article and Find Full Text PDFEur J Pain
October 2025
Department of Neurosurgery, AZ Delta Hospital, Roeselare, Belgium.
Background: Spinal cord stimulation (SCS) is a well-established treatment for chronic neuropathic and ischaemic pain. Although patient-reported outcomes have increasingly gained recognition, the impact of SCS on informal caregivers-an equally important consideration-remains underexplored. This study aims to address this gap by evaluating multidimensional outcomes following SCS, with a particular focus on the burden experienced by informal caregivers over a one-year period.
View Article and Find Full Text PDFClin Ophthalmol
August 2025
State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, People's Republic of China.
Purpose: To evaluate the caregiver burden and its associated factors among patients receiving anti-VEGF intravitreal injections for age-related macular degeneration (AMD) and diabetic retinopathy (DR) in a tertiary hospital in Guangzhou, China.
Methods: This cross-sectional study recruited 88 patients who received intravitreal anti-VEGF injections and their primary caregivers. Patients completed the Activities of Daily Living (ADL) scale, while caregivers completed the Zarit Burden Interview (ZBI) and the Connor-Davidson Resilience Scale (CD-RISC).