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Research on Users’ Views about Stroke Services: Towards an Empowerment Research Paradigm or More of the Same?

Research output: Contribution to Journal/MagazineJournal articlepeer-review

<mark>Journal publication date</mark>1996
Issue number1
Number of pages7
Pages (from-to)6-12
Publication StatusPublished
<mark>Original language</mark>English


The findings of two small-scale qualitative research projects about the health needs of people with stroke are used to introduce and discuss key concepts which frame current debates about the health care professional’s role and relationship to consumers of health care, the place of ‘user view’ research and the ‘consumer voice’ in health needs assessment, and the political nature of research on chronic illness and disability.