Peer reviewed journal articles

  1. Carter P, Martin G. Engagement of patients and the public in NHS sustainability and transformation: an ethnographic study. Critical Policy Studies (2017)
  2. Martin G, Carter P, Dent M. Major health service transformation and the public voice: conflict, challenge or complicity? Journal of Health Services Research and Policy (2017)

Reports / conference proceedings

  • Carter P. (2016). Participation, involvement and engagement – more than a question of semantics. International Sociological Association conference 2016. Vienna.
  • Carter P, Martin G. (2015) Managing Patient and Public Involvement in Polycentric Governance: An Institutional Logics Approach. Is there an alternative? Management After Critique.
  • Carter P, Brown L, Parker M, Martin G, Dixon-Woods M. (2013). In confidence: an exploratory qualitative study of the social licence for epidemiological and clinical research. Changing society BSA annual conference 2014.
  • Carter P, Jinks C, Robinson A, Dobel-Ober D. (2010). The Research Design Service and the patient and public involvement agenda”. INVOLVE. Nottingham.
  • Carter P, Edelstyn N. (2012, November 13). The patients, the professional researcher and the PPI adviser: How we helped to design a study for Parkinson’s Disease patients. INVOLVE 2012. Eastleigh
  • Jinks C, Carter P, Higginbottom A, Redwood S, Stevenson F, Jowett S, Chuter A. Meanings, costs and consequences of PPI. School for Primary Care Research 2012 Showcase Abstract book (pp. 91).
  • Carter P. (2008, September 11). Jane’s story: A governmental narrative of work to welfare. In Dilemmas in Human Services. London.
  • Carter P. (2007, September 6). Four Symbols and a Situation. In Ethnographic Futures. Liverpool.
  • Carter P, Beech R, Ong BN, Jinks C. (2012, November 13). An evaluation of how people with musculoskeletal conditions are actively involved in research. In INVOLVE 2012. Nottingham: INVOLVE.
  • Jinks C, Carter P. (2011, September 14). A case study to evaluate patient and public involvement in musculoskeletal research. Med Soc. Chester, UK.
  • Carter P. (2012, June 18). “I think you should really look into this”: understanding how patients responded to a survey of their priorities for research and how a mixed methods team approached free text analysis. Mixed Methods International conference. Leeds.
  • Carter P. (2010, October). “Evaluating Patient and Public Involvement in Research: Methodological Considerations”. European Evaluation Society. Prague.
  • Ashmore C, Carter P, Jinks C, Ong P, Rhodes R. (2010) Supporting patient and public involvement (PPI) in research: the role of a user support worker Examples of training and support for public involvement in research. Eastleigh: INVOLVE
  • Carter P. (2008) “Jane’s story: A governmental narrative of work to welfare” conference proceedings, Dilemmas in Human Services. ISBN 978-1-905858-17-0

Share this page: