Abstract:Despite the acknowledgement that mental health inequalities are shaped by the interaction of macro-level (structural) and micro-level (individual, agentic) powers, dominant paradigms in mental health research have been ill-equipped to integrate those different levels of influence theoretically and empirically. As a result, an 'explanatory deficit' persists as to the causal mechanisms underpinning the impact of social inequalities on mental well-being, particularly mental health recovery. To redress this gap, c… Show more
“…Leamy’s personal recovery framework CHIME (Connectedness, Hope and optimism, Identity, Meaning, Empowerment) is one such model [ 55 ]. However, recent research has argued that such models cannot address structural disadvantages or social marginalisation that a person with SMI might face [ 56 ]. Current models also fail to capture the organisational barriers that need addressing in order to promote recovery-oriented care.…”
Section: Discussionmentioning
confidence: 99%
“…Aside the above three elements of the framework, it is important to identify and tackle the root causes such as discrimination, social stigma and resultant isolation, unemployment-generated poverty, and social inequality that perpetuate poor health conditions in people with SMI. Recent research has demonstrated that personal recovery models do not reflect these broader social structural problems [ 53 , 56 , 65 ], and as a result, fail to achieve sustainable outcomes. Trauma and iatrogenic trauma are other dismaying causes that require close attention if we want genuine changes in service users’ health behaviours [ 66 ].…”
People with severe mental illness (SMI) die significantly earlier than their well counterparts, mainly due to preventable chronic conditions such as cardiovascular disease (CVD). Based on the existing research, this perspective paper summarises the key contributors to CVD in people with SMI to better target the areas that require more attention to reduce, and ultimately resolve this health inequity. We discuss five broad factors that, according to current international evidence, are believed to be implicated in the development and maintenance of CVD in people with SMI: (1) bio-psychological and lifestyle-related factors; (2) socio-environmental factors; (3) health system-related factors; (4) service culture and practice-related factors; and (5) research-related gaps on how to improve the cardiovascular health of those with SMI. This perspective paper identifies that CVD in people with SMI is a multi-faceted problem involving a range of risk factors. Furthermore, existing chronic care or clinical recovery models alone are insufficient to address this complex problem, and none of these models have identified the significant roles that family caregivers play in improving a person’s self-management behaviours. A new framework is proposed to resolve this complex health issue that warrants a collaborative approach within and between different health and social care sectors.
“…Leamy’s personal recovery framework CHIME (Connectedness, Hope and optimism, Identity, Meaning, Empowerment) is one such model [ 55 ]. However, recent research has argued that such models cannot address structural disadvantages or social marginalisation that a person with SMI might face [ 56 ]. Current models also fail to capture the organisational barriers that need addressing in order to promote recovery-oriented care.…”
Section: Discussionmentioning
confidence: 99%
“…Aside the above three elements of the framework, it is important to identify and tackle the root causes such as discrimination, social stigma and resultant isolation, unemployment-generated poverty, and social inequality that perpetuate poor health conditions in people with SMI. Recent research has demonstrated that personal recovery models do not reflect these broader social structural problems [ 53 , 56 , 65 ], and as a result, fail to achieve sustainable outcomes. Trauma and iatrogenic trauma are other dismaying causes that require close attention if we want genuine changes in service users’ health behaviours [ 66 ].…”
People with severe mental illness (SMI) die significantly earlier than their well counterparts, mainly due to preventable chronic conditions such as cardiovascular disease (CVD). Based on the existing research, this perspective paper summarises the key contributors to CVD in people with SMI to better target the areas that require more attention to reduce, and ultimately resolve this health inequity. We discuss five broad factors that, according to current international evidence, are believed to be implicated in the development and maintenance of CVD in people with SMI: (1) bio-psychological and lifestyle-related factors; (2) socio-environmental factors; (3) health system-related factors; (4) service culture and practice-related factors; and (5) research-related gaps on how to improve the cardiovascular health of those with SMI. This perspective paper identifies that CVD in people with SMI is a multi-faceted problem involving a range of risk factors. Furthermore, existing chronic care or clinical recovery models alone are insufficient to address this complex problem, and none of these models have identified the significant roles that family caregivers play in improving a person’s self-management behaviours. A new framework is proposed to resolve this complex health issue that warrants a collaborative approach within and between different health and social care sectors.
“…They can be thought of as “potentialities” inherent in structures which might manifest overtly. That is, depending on the conditions that facilitate the actualization of a structure's causal potential, they may or may not have an observable impact at the empirical level (Karadzhov, 2019). Some of this insight stems from the identification of deep generative processes as vertical explanations recognized between the layers of stratified reality we have previously discussed—the real, actual, and empirical levels.…”
Section: Critical Realismmentioning
confidence: 99%
“…Deepening our understanding of how structural factors trickle down to poor personal well‐being, marginalization, and welfare should therefore become an urgent priority (Karadzhov, 2019). For the purposes of this paper “structural” or “structures” refer to social relations (economic–political–cultural–affective) which have causal powers, capable of change, continuous reproduction and transformation which can be seen or unseen in how they impact individual agency (Jones, 2001).…”
To uncover pathways for understanding and alleviating poverty, this paper offers an alternative approach for examining the real and unseen processes of destitution and in-work poverty which shape the lives of consumers. We apply a critical realist paradigm structured around three core tenets-stratified realities, complex causations and generative structures-to surface the nuanced complexities of these issues. A critical realist lens encourages impact by focusing on the deep causes of enduring social problems and provides transformative consumer research scholars with an integrative way to work toward transformative policy action.
“…By examining the agency-structure nexus, critical realist and the capabilities approach informed research could help illuminate the role of structural configurations that generate inequality, impede clinical recovery, and limit the embodied experience of the aspects of personal recovery we identified. Such research may further clarify the clinical-personal recovery relationship, help identify and remove oppressive structures, and guide ameliorative social change [55,56]. As clinical recovery's influence may differ depending when meaning-making occurs, studies exploring the relationship at different time points post psychiatric diagnosis would be helpful.…”
Section: Limitations and Future Directionsmentioning
Purpose
Long-term data on recovery conceptualisation in psychotic illness are needed to support mental health services to organise themselves according to recovery-oriented frameworks. To our knowledge, no previous research has investigated how first-episode psychosis (FEP) service users (sampled across psychotic illness type) perceive recovery beyond 5 years after diagnosis. We aimed to explore personal recovery meaning with individuals 20 years after their FEP and examine the potential influence of clinical recovery status on how they defined recovery (i.e. personal recovery).
Methods
Twenty participants were purposefully sampled from an epidemiologically representative FEP incidence cohort. At 20-year follow-up, semi-structured interviews were conducted with 10 cohort members who met full ‘functional recovery criteria’ (Clinically Recovered Group) and 10 who did not (Not Clinically Recovered Group). A thematic analysis was performed to develop shared themes and group-specific sub-themes to capture agreement and divergence between groups.
Results
Five shared themes were produced: pursuing balance in conflict, generating meaning in life, experiencing a dynamic personal relationship with time, redressing inequality while managing added challenges/vulnerability, and directing life from resilience to flourishing. The five group-specific sub-themes developed illuminate differences in the meaning ascribed to personal recovery by each group.
Conclusion
Findings emphasise the role of time in how personal recovery is conceptualised by service users and identify ways clinical recovery may influence personal recovery meaning in FEP at mid-later life. Mental health services failing to consider temporal changes in meaning-making and discounting clinical recovery risk ignoring key factors affecting personal recovery.
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