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The Quality of Life of Persons With Chronic Fatigue Syndrome
Abstract
This descriptive study used a between-methods triangulation design to analyze the multiple dimensions of quality of life in persons with chronic fatigue syndrome (CFS). This method, which refers to the combination of both quantitative and qualitative methods in the same study, allowed the authors to obtain more comprehensive and robust data than could be obtained by either method alone. A convenience sample of 110 persons with CFS completed the quality of life index and CFS questionnaire, and a subset of 22 persons were interviewed regarding their lived experience with CFS. Overall scores on the quality of life index were significantly lower in CFS than for other chronic illness groups. Subjects reported the lowest quality of life scores in health and functioning domain. Indepth interviews provided a more complete understanding of the quality of life in CFS and further explained the low ratings that were found on the quality of life index. The findings suggest that quality of life is particularly and uniquely disrupted in CFS.
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“Research shows that the QoL is lower in CFS patients compared with other chronic ill and healthy control groups [35-37].”
From Cognitive behavior therapy in patients with chronic fatigue syndrome: The role of illness acceptance and neuroticism. (2013) · cites this paper as [37]
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Metadata
- Authors
- ANDERSON, J. S., & FERRANS, C. E.
- Affiliations
- University of Illinois Chicago (US)
- Venue
- The Journal of Nervous & Mental Disease
- Published
- 1997-06
- Volume
- 185
- Issue
- 6
- Pages
- 359-367
- ISSN
- 0022-3018 (ISSN-L)
- OpenAlex
- W2090187894
- Cited by
- 227
- References
- 19
- Citations by year
- 2026: 1 · 2025: 4 · 2024: 4 · 2023: 1 · 2022: 1 · 2021: 4 · 2020: 3 · 2019: 6 · 2018: 4 · 2017: 9 · 2016: 5 · 2015: 16 · 2014: 8 · 2013: 7 · 2012: 7
- FWCI
- 5.16
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Nervous and Mental Disease (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Fibromyalgia and Chronic Fatigue Syndrome Research
- Health Sciences › Medicine › Clinical Neurology › Long-Term Effects of COVID-19
- Health Sciences › Medicine › Clinical Neurology › Traumatic Brain Injury Research
- Keywords
- chronic fatigue syndrome, quality of life, lived experience, quality of life index, health and functioning, chronic disease, patient-reported outcomes
- MeSH terms
- Adolescent, Adult, Aged, Attitude to Health, Employment, Family, Female, Health Status Indicators, Humans, Income, Male, Middle Aged, Psychometrics, Quality of Life, Surveys and Questionnaires, Social Support, Fatigue Syndrome, Chronic, Sickness Impact Profile
About these checks
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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