ArticleBMC research notes2016
The association between caregiver well-being and care provided to persons with Alzheimer's disease and related disorders.
Article in BMC research notes, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
6 citing papers in PubMed.
- Relieving care burden and promoting health-related quality of life for family caregivers of elderly people with Alzheimer's disease via an empowerment program.Aging clinical and experimental research · 2023Trial
- Distribution of Informal Caregiving for Older Adults Living With or At Risk of Cognitive Decline Within and Beyond Family in Rural South Africa.The journals of gerontology. Series B, Psychological sciences and social sciences · 2025Article
- Alcohol Use and Abuse Among Family Caregivers of People Living with Dementia in the United States: A Scoping Review.International journal of environmental research and public health · 2024Article
- Family caregiver quality of life and the care provided to older people living with dementia: qualitative analyses of caregiver interviews.BMC geriatrics · 2022Article
- Measuring quality and level of care provided by family caregivers of persons with dementia: protocol for a systematic review of validated instruments.AIMS public health · 2021Article
- Clinical and Demographic Predictors of Adverse Outcomes in Caregivers of Patients with Dementia.Dementia and neurocognitive disorders · 2019Article
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
backgroundAlzheimer's disease and related disorders (ADRD) are some of the leading causes of morbidity in developed nations. Unpaid family caregivers are primarily responsible for providing the care and support needed by persons with ADRD. In the process of caring for their loved ones with ADRD, caregivers often have to deal with multiple challenges, including their own deteriorating well-being and overall quality-of-life (QoL). A recent systematic review showed that very little research has been undertaken to study the relationship between AD caregiver QoL and the level or quality of care that caregivers provide to their loved ones. In this study, we investigate the relationships between caregiver well-being and the care provided to persons with ADRD.
methodsWe used 12-month follow-up data from the Philadelphia site (n = 125) of the National Institutes of Health (NIH) multi-site study, Resources for Enhancing Alzheimer's Caregiver Health (REACH I) to examine the relationship between caregiver well-being and the level or quality of care provided while adjusting for important covariates (e.g., age, income, and years since caregiving). Caregivers who participated in REACH I had to be at least 21 years of age and they had to be providing at least 4 h of care per day for 6 months or more to a live-in loved one with ADRD. Linear regression analysis was used to examine the relationships between well-being and the level or quality of care provided to persons with ADRD.
resultsOf the 255 caregivers who participated in the REACH I study, 125 (49.0 %) remained after 12 months of follow-up. Comparisons of participants at the 12-month follow-up and participants who were lost to follow-up showed that these two sets of participants were not statistically significantly different on any of the variables examined in this study. Linear regression analysis showed that there was no statistically significant association between caregiver well-being and level or quality of care provided.
conclusionsFurther research is required to investigate the factors associated with level and quality of care provided to persons with ADRD, and whether caregiver well-being (or QoL in general) is a contributor.
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