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Caregiver burden in end-stage kidney disease requires assessment using validated instruments. This systematic review evaluated measurement properties of caregiver burden instruments in end-stage kidney disease using Consensus-Based Standards for the Selection of Health Measurement Instruments methodology. We searched 8 databases (PubMed, CINAHL, Embase, Web of Science, MEDLINE, Cochrane Library, Scopus, and PsycINFO) for studies evaluating measurement properties of caregiver burden instruments in caregivers of patients with kidney failure. The Consensus-Based Standards for the Selection of Health Measurement Instruments Risk of Bias checklist assessed methodological quality, and Grading of Recommendations Assessment, Development and Evaluation approach evaluated evidence quality. Twenty-four studies evaluating 21 distinct caregiver burden instruments were included. The Zarit Burden Interview, Caregiver Burden Scale, and Beck Depression Inventory were most frequently evaluated. Only a few instruments had high-quality evidence of sufficient content validity, internal consistency, test-retest reliability, and construct validity. Cross-cultural validity was assessed for only 9 instruments, with most rated as indeterminate owing to methodological limitations. No studies evaluated responsiveness to change over time. Quality of evidence was low to very low for most measurement properties, highlighting significant gaps in validation research. The Zarit Burden Interview, Caregiver Burden Scale, and Beck Depression Inventory show promising validity and reliability but require further testing. Rigorously conducted validation studies, involvement of caregivers of patients with kidney failure in content validation, and cross-cultural adaptations are priorities for optimizing burden assessment in this unique population.
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http://dx.doi.org/10.1016/j.xkme.2025.101054 | DOI Listing |
JMIR Res Protoc
September 2025
Institute for Collaboration on Health, Intervention, and Policy, University of Connecticut, Storrs, CT, United States.
Background: Children in the United States have poor diet quality, increasing their risk for chronic disease burden later in life. Caregivers' feeding behaviors are a critical factor in shaping lifelong dietary habits. The Strong Families Start at Home/Familias Fuertes Comienzan en Casa (SFSH) was a 6-month, home-based, pilot randomized-controlled feasibility trial that aimed to improve the diet quality of 2-5-year-old children and promote positive parental feeding practices among a predominantly Hispanic/Latine sample.
View Article and Find Full Text PDFGerontologist
September 2025
Department of Psychiatry, University of Rochester Medical Center, Rochester, NY, 14642, USA.
Background And Objectives: Over 12% of older Latinos in the United States have Alzheimer's disease and related dementias (ADRD), facing earlier onset of the disease and severe symptoms compared to non-Hispanic Whites. These disparities in ADRD among Latinos can lead to significant caregiver strain and burden in Latino ADRD caregivers. Notably, Latino ADRD caregivers have poor overall health outcomes and face systemic inequities including limited access to quality dementia care resources that impact their well-being significantly.
View Article and Find Full Text PDFDisabil Rehabil Assist Technol
September 2025
Department of Special Needs Education and Rehabilitation, Department Pedagogy and Didactics for People with Physical and Motor Development Impairments and Chronic and Progressive Illnesses, Carl von Ossietzky University, Oldenburg, Germany.
Objectives: Many studies investigate the impact of assistive devices and technologies (AD/AT) on physical outcomes. The role of AD/ATs in everyday activities and participation of children with cerebral palsy (CP) has received much less attention. This review scopes the impact of AD/ATs by the activities and participation components of the International Classification of Functioning, Disability and Health (ICF) model.
View Article and Find Full Text PDFCureus
August 2025
Psychiatry and Behavioral Sciences, West Virginia University, Morgantown, USA.
This study examined whether caregivers of male or female patients with epilepsy differ in perceived burden, social support, and coping mechanisms. In a cross-sectional design conducted at a tertiary neuropsychiatric hospital, 60 caregivers (30 per group) completed the Family Burden Interview Schedule (FBIS), the Social Support Questionnaire (SSQ), and the Ways of Coping Questionnaire (WCQ). Caregivers of female patients reported greater financial strain and more pronounced impacts on mental and physical health, yet they also perceived higher levels of social support.
View Article and Find Full Text PDFJ Med Internet Res
September 2025
Dementia Care and Research Center, Peking University Institute of Mental Health (Sixth Hospital), Beijing, China.
Background: Informal caregivers of home-dwelling people with dementia experience significant unmet needs. However, family physician teams as primary health care gatekeepers for aging populations in China remain an underused resource for structured caregiver support.
Objective: This hybrid effectiveness-implementation study aimed to evaluate a policy-aligned integration of the World Health Organization's iSupport web-based program with China's family physician contract services for informal dementia caregivers while systematically assessing implementation determinants using the Consolidated Framework for Implementation Research (CFIR).