The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.
Caregiver burden and patients’ perception of being a burden in ALS
Abstract
The determinants of ALS caregiver burden and the feeling of the patients as being a burden were assessed using the Caregiver Burden Inventory and the Self-Perceived Burden Scale in 60 caregiver-patient couples. Caregiver burden was correlated to their level of depression and quality of life and, differently from other chronic disorders, increased with the worsening of patients' disability. ALS patients have a good objective perception of their impact on caregivers.
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“Quality of life may be increased and perceived carer burden decreased in MND family carers who find positive meaning [13,14] and have a sense of hope [18].”
From Feasibility, acceptability and potential effectiveness of dignity therapy for family carers of people with motor neurone disease (2014) · cites this paper as [18]
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Metadata
- Authors
- Chiò, A., Gauthier, A., Calvo, A., Ghiglione, P., & Mutani, R.
- Affiliations
- From the Department of Neuroscience (Drs. A. Chiò, A. Gauthier, A. Calvo, A. Ghiglione, and R. Mutani), University of Turin, and IRCCS Istituto Auxologico Italiano (Dr. R. Mutani), Piancavallo, Italy.
- IRCCS Istituto Auxologico Italiano (IT)
- ORCID
- Calvo, A.
- Venue
- Neurology
- Published
- 2005-05-24
- Volume
- 64
- Issue
- 10
- Pages
- 1780-1782
- ISSN
- 0028-3878 (ISSN-L)
- 1526-632X
- OpenAlex
- W2080752676
- Cited by
- 223
- References
- 9
- Citations by year
- 2026: 8 · 2025: 6 · 2024: 11 · 2023: 10 · 2022: 5 · 2021: 19 · 2020: 15 · 2019: 8 · 2018: 11 · 2017: 11 · 2016: 10 · 2015: 16 · 2014: 13 · 2013: 4 · 2012: 16
- FWCI
- 22.70
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neurology (publishedVersion)
- PubMed (publishedVersion)
- Institutional Research Information System University of Turin (University of Turin) (submittedVersion)
- Topics
- Health Sciences › Nursing › Research and Theory › Nursing care and research
- Health Sciences › Medicine › Clinical Neurology › Amyotrophic Lateral Sclerosis Research
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Keywords
- amyotrophic lateral sclerosis, caregiver burden, perceived burden, depression, quality of life, disability progression, Caregiver Burden Inventory
- MeSH terms
- Activities of Daily Living, Adult, Age Factors, Aged, Amyotrophic Lateral Sclerosis, Chronic Disease, Depression, Female, Humans, Male, Middle Aged, Patients, Quality of Life, Surveys and Questionnaires, Sex Factors, Social Support, Caregivers, Disease Progression, Spouses
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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