Abstract

AbstractThe social inclusion of people with dementia (PwD) is recognised as a global goal of legislation, societal initiatives and service provision. Ensuring the social inclusion of PwD in these areas implies that its dimensions and domains are clear and unambiguous. However, the concept of social inclusion as it is currently used by researchers and practitioners is often vague or acts as a container concept for a variety of different approaches. This paper reports on an integrative review that analysed qualitative and quantitative studies on social inclusion and exclusion of PwD. It focused not only on the empirical results of the included studies but also on the theoretical embedding and methodological approaches to the concept of social inclusion and exclusion. We find that empirical studies on the social inclusion of PwD are scarce and largely characterised by a lack of or inconsistent conceptualisation. Against this background, the operationalisation of the concept and the assessment of the individual aspects of social inclusion with standardised instruments seem to be premature. Substantial theoretical and methodological work is needed to guide research on the social inclusion of PwD. The empirical results show that relationships with other people and being integrated into social networks are essential aspects of social inclusion. Likewise, the strategies and attitudes of caring persons can help to create or reinforce exclusion.

Highlights

  • For many years, research on dementia has focused primarily on the pathophysiological changes of the brain that lead to symptoms such as impaired memory, reasoning and comprehension (Plum, 1986: 2)

  • To investigate how social inclusion of people with dementia (PwD) has been researched, this paper reports on an integrative review that analysed qualitative and quantitative studies on social inclusion and exclusion of PwD

  • We aim to describe the use of the concept of ‘social inclusion of people with dementia’ in empirical studies

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Summary

Introduction

Research on dementia has focused primarily on the pathophysiological changes of the brain that lead to symptoms such as impaired memory, reasoning and comprehension (Plum, 1986: 2). This ‘standard paradigm’ was criticised by Kitwood (1997: 20) for neglecting changes in the social-psychological environment. The ability to adapt socially to the changes of dementia and to manage to have a good quality of life despite some limitations is one of the dimensions of social health as proposed by Huber et al (2011). To what extent social inclusion is already the subject of empirical dementia-related research is unclear

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