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Measuring the impact of patient and public involvement : the need for an evidence base
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Staniszewska, Sophie, Herron-Marx, Sandy and Mockford, Carole (2008) Measuring the impact of patient and public involvement : the need for an evidence base. International Journal for Quality in Health Care, Vol.20 (No.6). pp. 373-374. ISSN 1353-4505
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Official URL: http://dx.doi.org/10.1093/intqhc/mzn044
| Item Type: | Journal Item |
|---|---|
| Subjects: | H Social Sciences > HV Social pathology. Social and public welfare R Medicine > R Medicine (General) |
| Divisions: | Faculty of Social Sciences > School of Health and Social Studies |
| Library of Congress Subject Headings (LCSH): | Patient participation -- Great Britain -- Research |
| Journal or Publication Title: | International Journal for Quality in Health Care |
| Publisher: | Oxford University Press |
| ISSN: | 1353-4505 |
| Date: | December 2008 |
| Volume: | Vol.20 |
| Number: | No.6 |
| Number of Pages: | 2 |
| Page Range: | pp. 373-374 |
| Identification Number: | 10.1093/intqhc/mzn044 |
| Status: | Peer Reviewed |
| Publication Status: | Published |
| Access rights to Published version: | Restricted or Subscription Access |
| Description: | Editorial |
| References: | 1. Coulter A, McGee H. The European Patient of the Future. Maidenhead, UK: Open University Press, 2003. 2. Staniszewska S, Jones N, Newburn M, Marshall S. User involvement in the development of a research bid: barriers, enablers and impacts. Health Expect 2007;10:173–83. 3. Dorfman P. Patient and Public Involvement Policy in the UK. NHS Centre for Involvement, University of Warwick, 2007. 4. Department of Health. The Local Government and Public Involvement in Health Act. 2007. 5. HTA Programme. Public involvement index. 2005. http://www. hta.nhsweb.nhs.uk/consumers/index.htm (date last accessed 4 June 2008). 6. Boote J, Telford R, Cooper C. Consumer involvement in health research: a review and research agenda. Health Policy 2002;61: 213–36. 7. Oliver SR, Rees RW, Clarke-Jones L. A multidimensional conceptual framework for analysing public involvement in health services research. Health Expect 2008;11:7–84. 8. Crawford M, Rutter D, Manley C et al. Systematic review of involving patients in the planning and development of health care. Br Med J 2002;325:1263–8. 9. Daykin N, Evans D, Petsoulas C, Sayers A. Evaluating the impact of patient and public involvement initiatives on UK health services: a systematic review. Evid Policy 2007;3:47–65. 10. Moher D, Schulz KF, Altman G (for the CONSORT Group). The Consort statement: revised recommendations for improving the quality of reports of parallel-group randomised trials. Lancet 2001;357:1191–4. 11. Streiner DL, Norman GR. Health Measurement Scales: A Practical Guide to their Development and Use. Oxford: Oxford University Press, 1995. |
| URI: | http://wrap.warwick.ac.uk/id/eprint/29020 |
Data sourced from Thomson Reuters' Web of Knowledge
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