Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Salvi, Giovanni
Jones, Julia
and
Ruggeri, Mirella
2005.
Systematic review of the role of service users as researchers in mental health studies.
Epidemiology and Psychiatric Sciences,
Vol. 14,
Issue. 4,
p.
217.
Sweeney, Angela
2005.
The Ethics of Survivor Research: Guidelines for the Ethical Conduct of Research Carried Out by Mental Service Users and Survivors
Alison Faulkner, Bristol: Policy Press, 2004, £9.95, 56 pp. ISBN: 1-86134-641-7.
Psychiatric Bulletin,
Vol. 29,
Issue. 10,
p.
398.
Thornicroft, Graham
and
Tansella, Michele
2005.
Growing recognition of the importance of service user involvement in mental health service planning and evaluation.
Epidemiologia e Psichiatria Sociale,
Vol. 14,
Issue. 1,
p.
1.
Tansella, M.
Amaddeo, F.
Burti, L.
Lasalvia, A.
and
Ruggeri, M.
2006.
Evaluating a community‐based mental health service focusing on severe mental illness. The Verona experience.
Acta Psychiatrica Scandinavica,
Vol. 113,
Issue. s429,
p.
90.
Lasalvia, A.
and
Ruggeri, M.
2007.
Assessing the outcome of community‐based psychiatric care: building a feedback loop from ‘real world’ health services research into clinical practice.
Acta Psychiatrica Scandinavica,
Vol. 116,
Issue. s437,
p.
6.
Lucock, Mike
Barber, Rosemary
Jones, Anthony
and
Lovell, Jacqui
2007.
Service users' views of self-help strategies and research in the UK.
Journal of Mental Health,
Vol. 16,
Issue. 6,
p.
795.
HUBBARD, G.
KIDD, L.
and
DONAGHY, E.
2008.
Involving people affected by cancer in research: a review of literature.
European Journal of Cancer Care,
Vol. 17,
Issue. 3,
p.
233.
Crone, Diane
and
Guy, Helen
2008.
‘I know it is only exercise, but to me it is something that keeps me going’: A qualitative approach to understanding mental health service users' experiences of sports therapy.
International Journal of Mental Health Nursing,
Vol. 17,
Issue. 3,
p.
197.
Tew, Jerry
2008.
Researching in Partnership.
Qualitative Social Work,
Vol. 7,
Issue. 3,
p.
271.
Martindale, S. J.
Chambers, E.
and
Thompson, A. R.
2009.
Clinical psychology service users' experiences of confidentiality and informed consent: A qualitative analysis.
Psychology and Psychotherapy: Theory, Research and Practice,
Vol. 82,
Issue. 4,
p.
355.
Gillard, Steve
Turner, Kati
Neffgen, Marion
Griggs, Ian
and
Demetriou, Alexia
2010.
Doing research together: bringing down barriers through the ‘coproduction’ of personality disorder research.
Mental Health Review Journal,
Vol. 15,
Issue. 4,
p.
29.
Storm, Marianne
Hausken, Kjell
and
Mikkelsen, Aslaug
2010.
User involvement in in‐patient mental health services: operationalisation, empirical testing, and validation.
Journal of Clinical Nursing,
Vol. 19,
Issue. 13-14,
p.
1897.
Kernick, David
and
Mitchell, Annie
2010.
Working with lay people in health service research: A model of co-evolution based on complexity theory.
Journal of Interprofessional Care,
Vol. 24,
Issue. 1,
p.
31.
Gillard, Steven
Borschmann, Rohan
Turner, Kati
Goodrich‐Purnell, Norman
Lovell, Kathleen
and
Chambers, Mary
2010.
‘What difference does it make?’ Finding evidence of the impact of mental health service user researchers on research into the experiences of detained psychiatric patients.
Health Expectations,
Vol. 13,
Issue. 2,
p.
185.
Gillard, Steve
Turner, Kati
Lovell, Kathleen
Norton, Kingsley
Clarke, Tom
Addicott, Rachael
McGivern, Gerry
and
Ferlie, Ewan
2010.
“Staying native”: coproduction in mental health services research.
International Journal of Public Sector Management,
Vol. 23,
Issue. 6,
p.
567.
Boote, Jonathan
Baird, Wendy
and
Beecroft, Claire
2010.
Public involvement at the design stage of primary health research: A narrative review of case examples.
Health Policy,
Vol. 95,
Issue. 1,
p.
10.
Goodman, Claire
Mathie, Elspeth
Cowe, Marion
Mendoza, Alex
Westwood, Daphne
Munday, Diane
Wilson, Patricia M
Crang, Clare
Froggatt, Katherine
Iliffe, Steve
Manthorpe, Jill
Gage, Heather
and
Barclay, Stephen
2011.
Talking about living and dying with the oldest old: public involvement in a study on end of life care in care homes.
BMC Palliative Care,
Vol. 10,
Issue. 1,
Barber, Rosemary
Beresford, Peter
Boote, Jonathan
Cooper, Cindy
and
Faulkner, Alison
2011.
Evaluating the impact of service user involvement on research: a prospective case study.
International Journal of Consumer Studies,
Vol. 35,
Issue. 6,
p.
609.
Boote, Jonathan
Baird, Wendy
and
Sutton, Anthea
2011.
Public involvement in the systematic review process in health and social care: A narrative review of case examples.
Health Policy,
Vol. 102,
Issue. 2-3,
p.
105.
Gillard, Steve
Borschmann, Rohan
Turner, Kati
Goodrich-Purnell, Norman
Lovell, Kathleen
and
Chambers, Mary
2012.
Producing different analytical narratives, coproducing integrated analytical narrative: a qualitative study of UK detained mental health patient experience involving service user researchers.
International Journal of Social Research Methodology,
Vol. 15,
Issue. 3,
p.
239.