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- W2162024500 abstract "To identify key health outcomes, beyond morbidity and mortality, regarded as important in children and young people with neurodisability, and their parents.Qualitative research incorporating a thematic analysis of the data supported by the Framework Approach; the International Classification of Functioning, Disability and Health (ICF) provided a theoretical foundation.The study was conducted in community settings.Participants were 54 children and young people with neurodisability: 50 participated in focus groups, and 4 in interviews; 53 parents participated: 47 in focus groups and 6 in interviews. Children/young people and parents were recruited through different networks, and were not related.Children/young people and parents viewed health outcomes as inter-related. Achievement in some outcomes appeared valued to the extent that it enabled or supported more valued domains of health. Health outcomes prioritised by both young people and parents were: communication, mobility, pain, self-care, temperament, interpersonal relationships and interactions, community and social life, emotional well-being and gaining independence/future aspirations. Parents also highlighted their child's sleep, behaviour and/or safety.Those responsible for health services for children/young people with neurodisability should take account of the aspects of health identified by families. The aspects of health identified in this study provide a basis for selecting appropriate health indicators and outcome measures." @default.
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- W2162024500 date "2014-04-01" @default.
- W2162024500 modified "2023-10-02" @default.
- W2162024500 title "Key health outcomes for children and young people with neurodisability: qualitative research with young people and parents" @default.
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- W2162024500 doi "https://doi.org/10.1136/bmjopen-2013-004611" @default.
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