The full report of this research, entitled, South Australian Suicide Postvention Project 2004: Report to Mental Health Services, is available from: http://hdl.handle.net/2440/37903 (168 pages).
Consumer participation: Ensuring suicide postvention research counts for end users
Article first published online: 27 JAN 2010
© 2010 Blackwell Publishing Asia Pty Ltd
International Journal of Nursing Practice
Volume 16, Issue 1, pages 7–13, February 2010
How to Cite
Wilson, A. (2010), Consumer participation: Ensuring suicide postvention research counts for end users. International Journal of Nursing Practice, 16: 7–13. doi: 10.1111/j.1440-172X.2009.01811.x
- Issue published online: 27 JAN 2010
- Article first published online: 27 JAN 2010
- Accepted for publication August 2009
- consumer participation;
- primary health care;
- suicide postvention
Wilson A. International Journal of Nursing Practice 2010; 16: 7–13 Consumer participation: Ensuring suicide postvention research counts for end users
Primary health-care research is about working with those who have a vested interest in the outcomes of that research, including consumers, service providers and service organizations. This article describes how consumers were included in the research processes of a South Australian study into suicide postvention services, and illustrates important principles to consider when including consumers in research. A concurrent mixed-method approach facilitated the collection of mixed data through the application of questionnaires. The study was conducted in an Australian metropolitan area. Because of media releases, a large number of people rang to enquire and volunteer their participation. From over 200 expressions of interest, 161 individuals participated. The participation of consumers in the research process ensured the findings were relevant for end users. A number of recommendations for the care and support of those bereaved through suicide were developed as a result.