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What is e-health (5) : a research agenda for eHealth through stakeholder consultation and policy context review

JONES, Ray
et al
November 2005

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This article reports a study that explored the concerns of professional and lay stakeholders regarding future developments of eHealth in the UK and reviewed relevant policy to produce recommendations for eHealth research. It concludes that the scope of eHealth research (grouped under four headings: using, processing, sharing, controlling information) derived empirically from this study corresponds with 'textbook' descriptions of informatics. Stakeholders would like eHealth research to include outcomes such as improved health or quality of life, but such research may be long term while changes in information technology are rapid. Longer-term research questions need to be concerned with human behavior and our use of information, rather than particular technologies A parallel literature review was carried out by others and has been reported elsewhere

Quebec classification : disability creation process

FOUGEYROLLAS, Patrick
et al
1999

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This book presents 'an explanatory model for the causes and consequences of disease, trauma and other disruptions to a person's integrity and development'. It approaches the challenge of creating a classification system from a perspective of social change, human rights and equal opportunities. Specific issues addressed in the book include: the person-environment interaction; positive concepts; disability as the situational result of social participation; extrinsic and intrinsic distinction (or environmental/situational versus personal dimensions); the ethics of applying the classification system in different situations

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