Socioeconomic disadvantage and self-reported health
Analysis examining how socioeconomic disadvantage affects transitions from good health to poorer health among the working-age population in England and Wales between 2011 and 2021.
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A cross-sectional study examining whether social care funding for people with intellectual disabilities is distributed equitably across English local authorities.
Key statistics
Key messages
Policy implications
Gaps
Commentary
This study identifies a clear equity issue in the distribution of social care funding for people with intellectual disabilities. Local authorities with higher levels of deprivation support more individuals with intellectual disabilities but do not receive or allocate proportionately greater resources. This mismatch between need and funding creates a structural disadvantage for people living in more deprived areas.
From a care equity perspective, this finding is particularly significant. When funding does not reflect population need, local authorities face constraints in service availability, workforce capacity and quality of provision. Over time, this risks entrenching place-based inequities, where access to adequate support depends on where a person lives rather than their level of need.
The absence of effects related to rurality or political leadership suggests that these inequities are systemic rather than incidental. This points towards national funding mechanisms that insufficiently weight deprivation and prevalence, rather than local decision-making alone. As a result, local authorities with the greatest challenges may be least able to respond effectively.
For people with intellectual disabilities, these structural funding gaps can translate into reduced access to personalised support, longer waiting times and greater pressure on families and unpaid carers. Without adjustment, funding arrangements risk reproducing inequality rather than mitigating it.
Addressing these inequities requires a shift towards needs-based resource allocation that explicitly recognises socioeconomic context. Ensuring equitable access to social care for people with intellectual disabilities depends not only on local practice, but on national systems that distribute resources in line with demand and complexity of need.
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Analysis examining how social policies in England and Wales fail to address the needs of Autistic adults, focusing on barriers in health services and social care systems.
A study examining safety inequities experienced by people with learning disabilities in English health and social care, drawing on lived experiences from focus groups and patient feedback narratives.
A systematic review examining interventions designed to reduce inequities in dementia diagnosis and post-diagnostic care across multiple countries, focusing on individual, community and health system solutions.
A qualitative study examining how newly qualified social workers in England experience and respond to racism in practice, and how social work education prepares them to challenge racism in health and social care contexts.
A national study exploring practical solutions to reduce inequalities in dementia diagnosis and care across England, drawing on workshops with people with dementia, carers, professionals and third sector organisations.
A policy-focused review examining barriers to dementia care access for Black and minoritised communities in the UK, highlighting gaps between national policy ambitions and local service delivery.