45
Views
6
CrossRef citations to date
0
Altmetric
RESEARCH

Consumer participation in mental health research: articulating a model to guide practice

&
Pages 237-241 | Published online: 06 Jul 2009

References

  • Human Rights and Equal Opportunity Commission. Human Rights and Mental Illness: Report of the National Inquiry into the Human Rights of People With Mental Illness. Australian Government Publishing Service, Canberra 1993
  • World Health Organisation. Consumer Participation Manual. A Document to Facilitate Consumer Participation in the Mental Health System. WHO, British Columbia 1993
  • Commonwealth of Australia. National Mental Health Plan. Australian Government Printer, Canberra 1992
  • Commonwealth of Australia. National Standards for Mental Health. Australian Government Printer, Canberra 1997
  • Commonwealth of Australia. Evaluation of the National Mental Health Strategy. Australian Government Publishing Service, Canberra 1998
  • National Health and Medical Research Council. Values and Ethics: Guidelines for Ethical Conduct in Aboriginal and Torres Strait Islander Health Research. NHMRC, Canberra 2003
  • Telford R, Faulkner A. Learning about service user involvement in mental health research. Journal of Mental Health 2004; 13: 549–559
  • Griffiths KM, Jorm AF, Christensen H. Academic consumer researchers: A bridge between consumers and researchers. Australian and New Zealand Journal of Psychiatry 2004; 38: 191–196
  • Philpot M, Collins C, Trivedi P, Treloar A, Gallacher S, Rose D. Eliciting users’ views of ECT in two mental health trusts with a user designed questionnaire. Journal of Mental Health 2004; 13: 403–413
  • Roper C. Consumer participation in mental health: we want it!. Health Issues 2003; 74: 19–22
  • Rose D. Having a diagnosis is a qualification for the job. British Medical Journal 2003; 326: 1331
  • Trivedi P, Wykes T. From passive subjects to equal partners – Qualitative review of user involvement in research. British Journal of Psychiatry 2001; 181: 468–472.
  • Knowles C. Bedlam on the Streets. Routledge, London 2000
  • Roper C. We are the evidence: consumer perspective in research. New Paradigm 2005; September issue. Available at: www.vicserv.org.au/publications/new_para/index.htm (accessed February 2006).
  • Entwistle VA, Renfrew MJ, Yearley S, Forrester J, Lamont T. Lay perspectives: advantages for health research. British Medical Journal 1998; 316: 463–466
  • Ochocka J, Janzen R, Nelson G. Sharing power and knowledge: professional and mental health consumer/survivor researchers working together in a participatory action research project. Psychiatric Rehabilitation Journal 2002; 25: 379–387
  • Goodare H, Lockwood S. Involving patients in clinical research improves the research. British Medical Journal 1999; 319: 1315–1318
  • Hanley B, Truesdale A, King A, Elbourne D, Chalmers I. Involving consumers in designing, conducting, and interpreting randomised controlled trials: questionnaire survey. British Medical Journal 2001; 322: 519–523
  • Lammers J, Happell B. Research involving mental health consumers and carers: a reference group approach. International Journal of Mental Health Nursing 2004; 13: 262–266

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.