Social inclusion of people with severe mental illness: a review of current practices, evidence and unmet needs, and future directions

Social inclusion means being able to participate in activities valued within one's community or wider society as one would wish. People with severe mental illness (i.e., psychoses, bipolar disorder, and severe depression) experience some of the highest rates of social exclusion compared to people with other disabilities. This is the case regardless of the availability of specialist mental health services. Therefore, questions arise about the extent to which mental health services can and do prioritize social inclusion as a goal of service provision, and what strategies are needed outside of mental health services, at the levels of legislation and policy, statutory services, and civil society. In this paper we consider what social inclusion means in different cultures and contexts, since the value attached to different activities varies by culture and by life stage and gender. We discuss the subjective impact of low levels of social inclusion in terms of loneliness, and the evidence base for interventions to address it. We then turn to strategies to increase observable forms of social inclusion, considering them at the levels of legislation, services and other community assets. While evidence for some interventions is largely based on the Global North, we use evidence and examples from the Global South to the extent that we have found them. We also consider the predominant frameworks for social inclusion used in health services, followed by alternatives that may offer a more empowering approach to social inclusion for some people. We then describe strategies to reduce social exclusion through interventions to address stigma and discrimination, directed at key target groups or at population level. We make recommendations for policy makers, researchers, health professionals, and advocates based on the evidence and examples we have found, covering various forms of legislation, services and mental health research. Our conclusions identify the next steps for interventions, including development, evaluation, implementation or modification for better contextual adaptation.

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Publication Details

Journal
World Psychiatry
Published
2026-01-14
DOI
https://doi.org/10.1002/wps.70031
Citations
10
Primary Topic
Mental Health and Patient Involvement
Type
article
Field-Weighted Citation Impact
460.24
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article

Social inclusion of people with severe mental illness: a review of current practices, evidence and unmet needs, and future directions

Anthony Salla, Jasmine Kalha, Gerald Jordan, Sebastian Hinde et al.
10 citations
World Psychiatry
Mental Health and Patient Involvement
460.24
article

Social inclusion of people with severe mental illness: a review of current practices, evidence and unmet needs, and future directions

Anthony Salla, Jasmine Kalha, Gerald Jordan, Sebastian Hinde, Mike Dominic Slade, Yasuhiro Kotera, LAURA BOJKE, Peter A. Coventry, Brynmor Lloyd‐Evans, Claire Henderson, Matthew Gorner
article en
10 citations

Abstract

Social inclusion means being able to participate in activities valued within one's community or wider society as one would wish. People with severe mental illness (i.e., psychoses, bipolar disorder, and severe depression) experience some of the highest rates of social exclusion compared to people with other disabilities. This is the case regardless of the availability of specialist mental health services. Therefore, questions arise about the extent to which mental health services can and do prioritize social inclusion as a goal of service provision, and what strategies are needed outside of mental health services, at the levels of legislation and policy, statutory services, and civil society. In this paper we consider what social inclusion means in different cultures and contexts, since the value attached to different activities varies by culture and by life stage and gender. We discuss the subjective impact of low levels of social inclusion in terms of loneliness, and the evidence base for interventions to address it. We then turn to strategies to increase observable forms of social inclusion, considering them at the levels of legislation, services and other community assets. While evidence for some interventions is largely based on the Global North, we use evidence and examples from the Global South to the extent that we have found them. We also consider the predominant frameworks for social inclusion used in health services, followed by alternatives that may offer a more empowering approach to social inclusion for some people. We then describe strategies to reduce social exclusion through interventions to address stigma and discrimination, directed at key target groups or at population level. We make recommendations for policy makers, researchers, health professionals, and advocates based on the evidence and examples we have found, covering various forms of legislation, services and mental health research. Our conclusions identify the next steps for interventions, including development, evaluation, implementation or modification for better contextual adaptation.

World PsychiatryVol. 25(1)
Birmingham City University (GB), City, University of London (GB), King's College London (GB), South London and Maudsley NHS Foundation Trust (GB), Indian Law Institute (IN), Nord University (NO), Institute of Mental Health (GB), Genesis Research Institute (JP), University College London (GB), University of York (GB), The University of Osaka (JP)
Reduced inequalities
Openalex Percentile: Top 0%
Mental Health and Patient Involvement
460.24
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