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Results of the 2006/2007 Hospice Patient Survey

Hastie, Charlotte L. and Jenkins, Linda M. (2007) Results of the 2006/2007 Hospice Patient Survey. Project report. Centre for Health Services Studies, Canterbury (KAR id:2887)

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Abstract

The National Minimum Standards for Independent Healthcare, published in 2002 by the Care Standards Commission (now the Healthcare Commission), states that hospices are required to conduct an annual patient survey. In response to this, a Patient Survey Group (with representation from independent

2006/2007. The self-complete survey incorporated questions relating to: information giving; staff attitudes; patient involvement in care planning; confidence in staff; privacy and respect; catering and hygiene; awareness of the process for complaints; and support when patients were discharged or had died. 1352 questionnaires were returned from daycare patients and 1052 from inpatients.

Item Type: Monograph (Project report)
Uncontrolled keywords: Patient, survey, daycare, services, hospice
Subjects: H Social Sciences > H Social Sciences (General)
H Social Sciences > HM Sociology
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: Paula Loader
Date Deposited: 05 Jun 2008 17:23 UTC
Last Modified: 16 Feb 2021 12:15 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/2887 (The current URI for this page, for reference purposes)
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