Wilson, Patricia M. (2013) Patient and Public Involvement in the English Clinical Commissioning Groups: Access, Agenda & Deliberation. In: Royal College of Nursing International Research Conference, 20-22 March 2013, Belfast. (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:39124)
| The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided. |
Abstract
Patient and public involvement (PPI) in health is globally acknowledged (IAPO 2005) and firmly embedded within England's Department of Health policies including the new Clinical Commissioning Groups. However, previous evaluations of PPI suggest that engagement is often tokenistic.
| Item Type: | Conference or workshop item (Paper) |
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| Subjects: | R Medicine > RA Public aspects of medicine |
| Divisions: | Divisions > Division for the Study of Law, Society and Social Justice > School of Social Policy, Sociology and Social Research > Centre for Health Services Studies |
| Depositing User: | Tony Rees |
| Date Deposited: | 09 Apr 2014 10:37 UTC |
| Last Modified: | 16 Nov 2021 10:15 UTC |
| Resource URI: | https://kar.kent.ac.uk/id/eprint/39124 (The current URI for this page, for reference purposes) |
University of Kent Author Information
Wilson, Patricia M..
| Creator's ORCID: |
 https://orcid.org/0000-0002-5787-9736
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