Consumer involvement in health research: Fact or fiction?

British Journal of Clinical Governance

Volumn 7, Issue 2, 2002, Pages 92-103

  Telford, R ^a   Beverley, C A ^a   Cooper, C L ^a   Boote, J D ^a,b  

^a UNIVERSITY OF SHEFFIELD   (United Kingdom)

^b SHEFFIELD HEALTH AND SOCIAL CARE NHS FOUNDATION TRUST   (United Kingdom)

Author keywords

Health care; National Health Service; R D; User studies

Indexed keywords

ACCURACY; ARTICLE; AWARENESS; CONSUMER; HEALTH CARE POLICY; HEALTH CARE UTILIZATION; HEALTH PROGRAM; HEALTH SURVEY; HUMAN; MEDICAL RESEARCH; NATIONAL HEALTH SERVICE; POLITICS; PRIORITY JOURNAL; RESOURCE MANAGEMENT;

EID: 0036277214     PISSN: 14664100     EISSN: None     Source Type: Journal    
DOI: 10.1108/14664100210427606     Document Type: Article

References (42)

1. The NHS and its users
2. Speaking up for ourselves. The evolution of consumer advocacy in health care
3. Critical appraisal skills programme
4. What do I want from health research and researchers when I am a patient?
5. Research: Who's Learning?
6. What is participatory research?
7. The National Research Register
8. Research and development
9. Research governance framework
10. Lay perspectives: Advantages for health research
11. Involving patients in clinical research
12. Consulting to involve or consulting to empower
13. Mismatches in priorities for health research between professionals and consumers
14. Involving consumers in designing, conducting and interpreting randomised controlled trials: Questionnaire survey
15. Who are you, and who are we? Looking through some key words
16. Whose priorities? Listening to users and the public
17. Minority ethnic community participation in needs assessment and service development in primary care: Perceptions of Pakistani and Bangladeshi people about psychological distress
18. User involvement in clinical audit: A review of developments and issues of good practice
19. Participatory research maximises community and lay involvement
20. BIOMED, Ovid Technologies
21. How can health service users contribute to the NHS research and development programme?
22. Exploring lay perspectives on questions of effectiveness
23. Involving consumers in a needs-led research programme: A pilot project
24. The lay perspective in health technology assessment
25. User involvement in mental health service development: How far can it go?
26. What does it mean to listen to people with dementia?
27. Consumer involvement in research is essential
28. Participatory research
29. Setting agendas for relevant research: A participatory approach