This book addresses the major theoretical and practical issues of the forms of citizenship and access to citizenship in different types of polity, and the specification and justification of rights of non-citizen immigrants as well as non-resident citizens. It also addresses the conditions under which norms governing citizenship can legitimately vary. The book discusses the principles of including all affected interests (AAI), all subject to coercion (ASC) and all citizenship stakeholders (ACS). They complement each other because they serve distinct purposes of democratic inclusion. The book proposes that democratic inclusion principles specify a relation between an individual or group that has an inclusion claim and a political community that aims to achieve democratic legitimacy for its political decisions and institutions. It contextualizes the principle of stakeholder inclusion, which provides the best answer to the question of democratic boundaries of membership, by applying it to polities of different types. The book distinguishes state, local and regional polities and argues that they differ in their membership character. It examines how a principle of stakeholder inclusion applies to polities of different types. The book illustrates the difference between consensual and automatic modes of inclusion by considering the contrast between birthright acquisition of citizenship, which is generally automatic, and naturalization, which requires an application.
Some questions for Rainer Bauböck
Joseph H. Carens
In this chapter, the author describes Rainer Bauböck's virtues and limitations of three different principles of democratic inclusion. The principles include all affected interests (AAI), all subject to coercion (ASC), and all citizenship stakeholders (ACS). Bauböck argues that the three principles complement one another, with each providing legitimation for a different set of democratic institutions and practices. He has many illuminating things to say about these three principles, including the ways in which they are derived from different but compatible conceptions of democracy. Bauböck also explores fundamental questions about what a just global political order would require from a democratic perspective. The primary purpose of democracy is to provide legitimacy to coercive political rule through popular self-government. Lots of people would argue that one can be committed to equality of rights and democratic inclusion without embracing the view of the legal rights of irregular migrants.
Results of the Charité Human Remains Project
Holger Stoecker and Andreas Winkelmann
From 2010 to 2013 the Charité Human Remains Project researched the provenance of the remains of fifty-seven men and women from the then colony of German South West Africa. They were collected during German colonial rule, especially but not only during the colonial war 1904–8. The remains were identified in anthropological collections of academic institutions in Berlin. The article describes the history of these collections, the aims, methods and interdisciplinary format of provenance research as well as its results and finally the restitutions of the remains to Namibia in 2011 and 2014.
Edited by: Penny Bee, Helen Brooks, Patrick Callaghan and Karina Lovell
This handbook is written for patients and members of the public who want to understand more about the approaches, methods and language used by health-services researchers. Patient and public involvement (PPI) in research is now a requirement of most major health-research programmes, and this book is designed to equip these individuals with the knowledge and skills necessary for meaningful participation. Edited by award-winning mental-health researchers, the book has been produced in partnership with mental-health-service users and carers with experience of research involvement. It includes personal reflections from these individuals alongside detailed information on quantitative, qualitative and health-economics research methods, and comprehensively covers all the basics needed for large-scale health research projects: systematic reviews; research design and analysis using both qualitative and quantitative approaches; health economics; research ethics; impact and dissemination. This book was developed during a five-year research programme funded by the UK’s National Institute for Health Research (NIHR) called Enhancing the Quality of User Involved Care Planning in Mental Health Services (EQUIP). The handbook clearly outlines research practices, and gives an insight into how public and patient representatives can be involved in them and shape decisions. Each chapter ends with a reflective exercise, and there are also some suggested sources of additional reading. People who get involved in health research as experts from experience now have a textbook to support their research involvement journey.
Helen Brooks and Penny Bee
Research activity does not finish when data analysis is complete. Once research findings are available, researchers still have obligations to fulfil. These obligations include sharing the findings with different audiences and ensuring maximum impact from the study. Dissemination refers to the active process of communicating research findings in a targeted and personalised way to identified relevant audiences who may be interested in the findings and/or able to benefit from them. This chapter describes some different ways in which research findings can be disseminated in order to increase the impact of research and ensure continued engagement with stakeholders.
Colonialism, grave robbery and intellectual history
Larissa Förster, Dag Henrichsen, Holger Stoecker and Hans Axasi╪Eichab
In 1885, the Berlin pathologist Rudolf Virchow presented three human skeletons from the colony of German South West Africa to the Berlin Society for Anthropology, Ethnology and Prehistory. The remains had been looted from a grave by a young German scientist, Waldemar Belck, who was a member of the second Lüderitz expedition and took part in the occupation of colonial territory. In an attempt to re-individualise and re-humanise these human remains, which were anonymised in the course of their appropriation by Western science, the authors consult not only the colonial archive, but also contemporary oral history in Namibia. This allows for a detailed reconstruction of the social and political contexts of the deaths of the three men, named Jacobus Hendrick, Jacobus !Garisib and Oantab, and of Belck’s grave robbery, for an analysis of how the remains were turned into scientific objects by German science and institutions, as well as for an establishment of topographical and genealogical links with the Namibian present. Based on these findings, claims for the restitution of African human remains from German institutions cannot any longer be regarded as a contemporary phenomenon only but must be understood as part of an African tradition of resistance against Western colonial and scientific practices.
Owen Price and Karina Lovell
Quantitative research uses large samples and, as such, the findings of well-conducted studies can often be generalised to larger populations. However, it is important that studies are well-designed to avoid errors in their interpretation and/or the reporting of inaccurate results. Misleading results from quantitative studies can have serious negative implications such as wasting public money on flawed policies and subjecting service users to ineffective or harmful treatments. This chapter explores descriptive and experimental quantitative research designs and examines, through case examples, the difference between cross-sectional, longitudinal and cohort studies. Factors leading to poorly and well-constructed studies are explored, along with a discussion of the key features of well-designed randomised controlled trials, the gold-standard design for testing treatment effectiveness.
Patrick Callaghan and Penny Bee
Quantitative data analysis makes sense of numerical data. We can use numbers to summarise the experiences or characteristics of a group of participants, for example their average age or the number of symptoms they report. We can also use numbers to look at people’s behaviours, experiences and views. Perhaps most importantly, we can use numbers to look at differences between groups of people or the same group over time. This can help us understand the effect of new treatment or policy initiatives, both in terms of the type of effect (e.g. does a new policy make things better, worse or leave things unchanged?) and the size of its impact (e.g. are any changes big enough to be meaningful or could they have happened just by chance?). This chapter explores some of the different approaches to analysing numerical data, examines the difference between descriptive and inferential statistics, and highlights some of the ways in which you can begin to interpret research data presented as numbers.
Designing and road testing new measurement scales
This chapter will examine the origins of measurement scales in research by considering the science of psychological testing. In particular the chapter provides a brief definition of a measurement scale, outlines why scales are used, examines the design and evaluation of scales, discusses what the responses to scales mean, outlines advantages and limitations of their use, and provides examples of measurement scales developed and used in the EQUIP project and other published mental health research. In recent years, as a response to criticisms that measurement scales are often not patient-oriented, we have seen increasing emphasis placed on the development of Patient Reported Outcomes Measures (PROMs). These tend to be less focussed on symptoms and more on the everyday experiences of people using services. They are much more likely to be designed and developed in collaboration with service users. The EQUIP research project developed a good quality PROM for assessing user and carer involvement in care planning, the first such measure of its kind in mental health.
Owen Price and Lauren Walker
It is of great importance that research projects are informed by sound ethics, properly planned, approved by an independent ethical board and rigorously monitored throughout the duration of the study. This chapter introduces four principles that govern the conduct of ethical research using relevant case examples to bring each principle to life. Topics explored include ‘informed consent’, capacity to provide consent, minimising and managing harm and the fair and equal treatment of study participants.