Research
You will find a complete range of our peer-reviewed monographs, multi-authored and edited works, including original scholarly research across the social sciences and aligned disciplines. We publish long and short form research and you can browse the Bristol University Press and Policy Press archive.
Policy Press also publishes policy reviews and polemic work which aim to challenge policy and practice in certain fields. These books have a practitioner in mind and are practical, accessible in style, as well as being academically sound and referenced.
Books: Research
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Available open access digitally under CC-BY-NC-ND licence.
Stigma has long been a central concern for social scientists studying health and illness. Yet, in existing work, stigma often escapes definition and clarification, is treated as universal and constant, and becomes a vague catch-all term for a range of conditions and situations.
This book initiates a process of recalibrating the conceptualisation of stigma. The book features original analyses from early- and mid-career scholars focusing on diverse issues, including mental health, racism, sex, HIV, reproduction, obesity, eating disorders, self-harm, exercise, drug use, COVID-19 and disability.
This ambitious book offers new perspectives to stimulate and intensify conversations around stigma, and highlights the valuable contributions of sociological approaches to the study of health and illness.
Available open access digitally under CC-BY-NC-ND licence.
Older adults’ civic engagement has become a key concern in academic and policy debates in recent years. However, existing studies on this topic remain fragmented across various conceptual and methodological approaches.
This book provides a comprehensive, interdisciplinary, and multidimensional perspective on older adults’ civic engagement. It proposes a conceptual framework which understands civic engagement as a multidimensional concept encompassing a diversity of activities through which older adults contribute to their communities and wider society. Contributors explore the factors shaping older adults’ participation in various civic activities across the life course, considering their diversity in terms of social locations such as gender, health status, migrant background, socioeconomic background and residential arrangements.
By analysing past and current research, policy and practice, the book offers recommendations for future efforts to advance the field.
The gap between personal and formal politics has been widening globally and locally. As personal politics have become more inclusive and egalitarian inspired by new social movements, neoliberal ideologies have undermined democracy, increasing isolation, inequality, poverty, disease and environmental threat. Yet this paradox may also offer a path to transformation.
Using international evidence and examples, The Antidote explores what we can learn from the equalisation of personal roles and relationships that’s been taking place, to help us reconnect with ourselves and each other and make possible more participatory and liberatory policy and politics. It sets out the barriers we face and offers a route map to bring an end to the destructive effects of unfettered neoliberal ideology, economics, policy and politics.
As populations age around the world, there is an urgent need to address the inadequate and unequal provision of care and support to older and disabled people.
This book represents the first collective effort to use the concept of care poverty to analyse unmet needs and inequalities in care at an international level and from a social policy perspective. It presents pioneering empirical studies and novel theoretical and methodological approaches to unmet needs and care poverty.
This volume points the way forward for international care research and, in particular, for the growing field of research on inadequate care and support.
Are we accepting of death, or in denial of it, and what can we learn, that might help us think and act meaningfully amidst the climate emergency, from the different ways death has been imagined, theorized and organized in Western social and intellectual history? Beginning with the role of tragedy, and then philosophy, in Greek antiquity, before exploring the history of European attitudes to death and their increasing entanglement with colonial atrocities and politically organized killing, this interdisciplinary study probes the work of philosophers, sociologists, historians and psychoanalysts to help make sense of mortality in the Anthropocene. Examining the denial of death discourse that was hegemonic in earlier mortality studies, it critically analyses the opposing argument that we are today more reconciled with the realities of death. Drawing on existential philosophy, Levinas’s theory of our responsibility for the death of others, and Harmut Rosa’s account of social acceleration and the catastrophe of resonance, Bowring highlights notable points of contact between anomic feelings of disappointment and missing out, growing climate anxiety and despair over the future conditions of life on earth, and the sense of wasted efforts and lost purposes that is characteristic of the midlife crisis. In response to this malaise he argues that we need to think of mortality as more than just a life of finite time, to recognize instead our shared vulnerability and passivity, and to understand how this makes us both dependent on others and responsible for other equally precarious forms of life.
This book explores the critical issue of how to manage the ever-increasing demand for social care in Britain’s ageing society. With informal care, from family members and friends, now the dominant form of adult social care in the UK, this precarious system is struggling to provide enough support.
Exploring the relationship between formal and informal care, this book develops ideas for a ‘caring economy’, showing the potential to integrate paid-for and unpaid care within a framework of solidarity based on the strengths of the community, working to improve the quality and quantity of state-funded care provision while sharing unpaid support more widely as a community responsibility.
Institutions play a crucial role in shaping experiences of end-of-life care, dying, death, body disposal and bereavement. However, there has been little holistic or multidisciplinary research in this area, with studies typically focusing on individual settings such as hospitals and cemeteries, or being confined to specific disciplines.
This interdisciplinary collection combines chapters on process, place and the past to examine the relationships both within and between institutions, institutionalisation and death in international contexts.
Of broad appeal to students and academics in areas including social policy, health sciences, sociology, psychology, anthropology, cultural studies, history and the wider humanities, this collection spans multiple disciplines to offer crucial insights into the end of life, body disposal, bereavement, and mourning.
The COVID-19 pandemic took many by surprise when it arrived in Britain in early 2020. Daily lives changed dramatically with the introduction of unprecedented restrictions and lockdowns. How did people react?
This book draws on the diaries of 68 men and women aged 70 and above, capturing their thoughts and experiences over the following months. Although these older diarists considered themselves among the more fortunate at the time, their entries reveal both highs and lows. There were anxieties and frustrations but also much positivity and, often, a reluctance for an over-hasty return to pre-pandemic times.
Through these personal and contemporaneous accounts, the book offers a unique contribution to our understanding of the pandemic and its significance in modern social history.
EPDF and EPUB available open access under CC-BY-NC-ND licence.
Civil society organizations (CSOs) and non-governmental organizations have increased at the United Nations (UN) since the 1990s. Yet few studies discuss the notion of inclusion and what it entails in intergovernmental negotiations.
This book delves into the UN’s relationship with CSOs, exploring who participates in negotiations and how their input is integrated into ratified documents. Drawing on ethnographic research, the author uncovers the complexities of accreditation, participation, and the interpretation of CSOs’ contributions. Offering a sociological analysis, she highlights the increased exclusion of CSOs despite their apparent inclusion in institutions of global governance unbounded to public accountability.
Leah R. Kimber examines the practices of exclusion CSOs are subjected to in UN negotiations by opening the machinery of intergovernmental negotiations in light of the UN’s future and legitimacy.
Dementia is one of the greatest challenges facing humanity in the 21st century. Responding to the global dementia challenge, however, affects more than humans alone. We live in a multi-species world but often think about dementia in mono-species ways. From the lab to the living room, other beings are “on the scene” and our relations with them affect how we understand, experience, and respond to dementia. Drawing on cutting-edge work across the social and biological sciences, this book offers readers the tools to respond to dementia in multi-species ways. By exploring a range of topics, from pathology to personhood, contributors highlight how thinking about dementia as a more-than-human phenomenon may enable new ways of responding to our global dementia challenge.
