Julian Ashton, Clare F. Aldus, Peter Richmond and Helen Allen
This paper aims to assess the current state, and various methods, of public and patient involvement, particularly but not exclusively in research on ageing and dementia.
Abstract
Purpose
This paper aims to assess the current state, and various methods, of public and patient involvement, particularly but not exclusively in research on ageing and dementia.
Design/methodology/approach
Interviews were carried out with a researcher, who has had a leading role in research on dementia; a public contributor with extensive relevant experience; and a member of the research design service with responsibility for patient and public involvement.
Findings
All those involved in the research can benefit considerably from public and patient involvement and it can make a significant difference to the course of a project. The importance of choosing an appropriate method of involvement is discussed and planning for it in both financial terms and time allowed. Examples are given of successful studies.
Research limitations/implications
Those who took part in the interviews were chosen for their record in furthering public and patient involvement in research. There is no attempt to compare their views with those of the wider research community.
Practical implications
The various ways in which patients and the public are involved in relevant research is a guide to those designing projects and those who may want to explore opportunities for involvement.
Social implications
Social implications include being able to influence research projects, contributors of all ages find they are valued.
Originality/value
The format of the paper is original, eliciting material from three viewpoints on research and involvement.
Details
Keywords
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Abstract
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Abstract
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