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- W2003600527 abstract "People with amyotrophic lateral sclerosis (ALS) frequently express dissatisfaction with services. Patient satisfaction with services in ALS care is not always measured and service user perspectives are not usually included when evaluating the outcomes of care. There is a lack of consensus on what constitutes satisfaction for patients in ALS care. To date, health care professionals’ conceptualization of outcomes in ALS care has excluded measures of patient satisfaction with services. Exploring the context of the ALS service user experience of care will identify a conceptual framework that will include the domains of satisfaction with care for patients with ALS. An instrument that draws on the ALS patient perspective of services, developed on the basis of qualitative investigation, should be used to measure satisfaction with services." @default.
- W2003600527 created "2016-06-24" @default.
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- W2003600527 creator A5027086651 @default.
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- W2003600527 date "2011-10-13" @default.
- W2003600527 modified "2023-10-10" @default.
- W2003600527 title "Experience of Services as a Key Outcome in Amyotrophic Lateral Sclerosis (ALS) Care" @default.
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- W2003600527 doi "https://doi.org/10.1177/1049909111423774" @default.
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