Abstract
Equitable involvement of patients and clinicians in setting research and funding priorities is ethically desirable and can improve the quality, relevance and implementation of research. Survey methods used in previous priority setting projects to gather treatment uncertainties may not be sufficient to facilitate responses from patients and their lay carers for some health care topics. We aimed to develop a new model to engage patients and clinicians in setting research priorities relating to life after stroke, and to explore the use of this model within a James Lind Alliance (JLA) priority setting project.
Original language | English |
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Pages (from-to) | 12-18 |
Number of pages | 7 |
Journal | Journal of Health Services Research and Policy |
Volume | 19 |
Issue number | 1 |
DOIs | |
Publication status | Published - Jan 2014 |
Keywords
- patients
- clinicians
- survey
- study model