To save content items to your account,
please confirm that you agree to abide by our usage policies.
If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account.
Find out more about saving content to .
To save content items to your Kindle, first ensure no-reply@cambridge.org
is added to your Approved Personal Document E-mail List under your Personal Document Settings
on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part
of your Kindle email address below.
Find out more about saving to your Kindle.
Note you can select to save to either the @free.kindle.com or @kindle.com variations.
‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi.
‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.
To decolonize social institutions (i.e. political, criminal justice, educational, and economic systems) a more profound commitment to inclusion and well-being will require a reimagining of the embedment of anti-racist and anti-oppressive paradigms. Various social institutions either inherited or created to meet the needs and aspirations of the former colonized, have faltered and failed under the pressures of Neo-Colonialism and structural racism, and have manifested in their various forms as structural adjustment programs, outsourcing, privatization of human services, and the rise of Non-Governmental Organizations (NGO’s). There is an urgent need for new and innovative research on the subject of producing a brave and adaptable generation of leaders who understand the value of servant leadership principles coupled with the principles of the Afrocentric Perspective as a framework to create social policies and engage in leadership practices that are sensitive to the needs of Black, Indigenous, and People of Color (BIPOC) and other oppressed groups in general as a conceptualization of a praxis of decoloniality. This chapter will address how these two approaches can contribute to the reinvigoration of upcoming leaders committed to serving BIPOC and other oppressed and marginalized groups.
People living with dementia (PLWD) want – and have the right – to participate in research that impacts them. However, barriers in legislation, institutional practices, and/or biases may jeopardize inclusion.
Objective and Methods
Interviews with 33 Canadian dementia researchers were conducted to explore understandings of research consent with regard to dementia, research practices, and approaches in everyday research contexts.
Findings
Analysis of these interviews revealed challenges in negotiating the space between best practices and institutional requirements; gaps in knowledge, procedures, and guidelines on inclusion and consent; tensions regarding who should be involved in decision making; and how assumptions of presumed incapacity and/or the ‘protection’ of vulnerable groups create and/or sustain the exclusion of PLWD from research.
Discussion
Moving forward, findings suggest that advancing the meaningful inclusion of PLWD in Canadian dementia research will require clear, consistent standardized guidelines, flexible and ongoing consent processes, accessibility accommodations, and a stronger focus on rights-based practices.
This Element argues for the benefits of integrating the perspectives of a new historiography of paleontology in the training of upcoming paleontologists and in the paleontological community's culture more broadly. Wrestling with the complex legacy of its past, the paleontological community is facing the need to reappreciate its history to address issues of accessibility and equity affecting the field, such as gender gap, parachute science, and specimen repatriation. The ability of the paleontological community to address these issues depends partly on the nature of its engagement with the past in which they find their source. This Element provides a conceptual toolkit to help with the interpretation of the unprecedented position in which the paleontological community finds itself regarding its past. It also introduces historiographical resources and provides some suggestions to foster collaboration between paleontology and the history of paleontology.
How much do we care when no one is looking? A patient with critical injury and vulnerable to bias—as an uninsured Person of Color experiencing homelessness and social isolation, with a history of mental illness and drug use— experiences barriers to receiving necessary treatment and standard care. When a patient is unable to ask for help, and has no family member or friend to help, what standard of care can they hope to receive? Can the quality of care provided to unrepresented patients represent a hospital’s culture of care? The writer wonders whether to “stay in my lane” and focus only on the ethical question prompting consultation, or if the principles of beneficence and nonmaleficence justify speaking up about substandard care. To mitigate the risk of acting as the “ethics police” by engaging in micromanagement of patient care, the writer describes efforts to expand ethics’ scope to change systemic and cultural attitudes by establishing preventative measures to identify and combat bias and preemptive judgments of futility.
The World Health Organization recognizes disability as part of being human. The fact that people with PICS are a part of a global disabled population at high risk of disparities due to disability itself is underrecognized.To better explore PICS as a subgroup within a larger disabled community, this chapter reviews international consensus on human rights and disability; the difference between equality and equity; the Biomedical and Social Models of Disability; application of the Social Model of Disability to the lived experiences of people with PICS; and practical strategies to make care more just and inclusive for people with PICS based on strategies that have been successful for other communities with disabilities.
The 1958–1965 period witnessed the rise and fall of the Great Leap Forward. During this period, China saw the second and most radical switch between decentralized and recentralized industrialization in the Mao era, and a further swing in labour policy towards promoting temporary employment. This chapter begins by presenting an overview of the economic and political circumstances of this period. It then examines how the rise and fall of the Great Leap Forward, combined with the shift in labour policy, dramatically redrew the exclusion system, thus affecting the scale and conditions of those in precarious urban employment.
The challenge of transitioning to a net-zero-carbon world requires engineers and scientists to blend their technical proficiency with soft skills such as trust-building, stakeholder influence, and effective leadership within multidisciplinary teams. This seamless integration of subject matter expertise and interpersonal skills — especially those focused on leadership — are essential for driving change. Unfortunately, these skills and knowledge are frequently left out of the foundational curriculum of science-based graduate programs across the United States. In order to accelerate the energy transition, we propose that our students receive instruction in developing skills required for effective implementation and leadership of change. This chapter will set up the framework for management and leadership training for STEM (science, technology, engineering, and mathematics) students or postdocs, whether in a two-hour workshop or a full semester course.
The scope, complexity, and interconnectedness of modern society should prompt us to develop dynamic understandings of democratic modes of inclusion and exclusion. In particular, democratic theory is becoming more attentive to the mismatch between those who make decisions and those who are affected by them as well as to the need to account for the voice of the latter. In this article I build on James Bohman’s understanding of democracy as a rule by multiple dêmoi to develop a framework for studying and evaluating modes of democratic inclusion that are based on being affected. To develop this framework I turn to law and public administration and examine the democratic properties of different institutions and procedures that give a voice to those who are affected by a decision.
The question of who ought to be included in the demos is distinct from, and yet related to, the question of how to distribute decision-making power among those who are included. Political equality is the most common answer to the former question within democratic theory. In democratic practice, it is usually realized through one person one vote. Within democratic theory, there is not as much agreement as to what the answer to the latter question should be. The answer that has attracted most attention within the scholarly literature is that all those who are affected should be included. However, prominent scholars have argued that this all-affected principle is incompatible with political equality and therefore an unattractive answer to the question of inclusion. This article challenges this critique and argues that it is based on a misconception of political equality and a narrow reading of the all-affected principle.
Museum visitors are not reflective of the diversity present in communities around the nation. In this study, we investigate the racial and ethnic diversity of art museum participants as well as the potential motivations and barriers to visiting a museum. Using the General Social Survey, we examine race and ethnicity and arts participation in the USA. We find Black individuals are less likely to attend an art museum than white individuals. Certain motivations and barriers to participating may explain part of the lack of diversity. We find Black and Latinx individuals are motivated to participate in art museums for cultural heritage reasons more than white individuals, but race and ethnicity are unrelated to perceiving admission fees as a barrier. This research highlights the urgency in the field to make museums more inclusive.
Volunteering is associated with health-promoting benefits for both recipients and volunteers and may contribute to a more inclusive society. However, studies have shown a persistent pattern of social inequality among those who volunteer, and immigrants participate as volunteers less than the majority population. To date, approaches for recruiting immigrant populations have not been sufficiently examined, even though multicultural societies are becoming increasingly diverse. This study investigates how recruitment is carried out in voluntary organizations and how volunteers who are involved in recruitment reflect on the inclusion of citizens with immigrant backgrounds. Qualitative interviews were conducted with 18 volunteers and three employees with recruitment responsibility at five voluntary organizations engaged in welfare and community-related activities in a semirural district in Norway. Our findings show that different structural factors and individual aspects of the recruiter influence the recruitment of immigrants as volunteers. Large-scale organizations are more professionalized and more directed by fundings and frameworks and demand more qualifications due to their volunteer tasks. This might make inclusive recruitment more challenging. Small-scale organizations have more flexibility and less professionalized volunteer activities, making recruitment more inclusive. In addition, if the small-scale organizations are minority driven, it seems to positively influence the recruitment of immigrants through increased diversity sensitivity and more connections with immigrants through their social network.
This response builds upon ideas introduced in Charity Hudley et al.'s (2020) target article by focusing on the themes of excellence and racial justice. In addition to relying on previous academic work on race and racism, I also draw from my own experiences as a person of color in the field of linguistics and as a scholar who works with racially minoritized communities. The primary claims of this paper are that the field of linguistics as a whole benefits from broadening and deepening our conceptualizations of scholarly excellence and from consciously attending to the needs and concerns of scholars and community members from racially minoritized groups. To support these claims, I discuss ways in which institutional structures of universities hinder equity and inclusion by marginalizing contributions of scholars from racially minoritized groups and by promoting extractive and neocolonial work involving minoritized communities. I conclude by offering general principles that can serve as guides for fostering greater diversity, equity, and inclusion in university settings. These principles involve acknowledging present shortcomings, aligning the reward system to a broadened notion of excellence and to inclusion, and embracing creative alternatives.
There are currently millions of people with Alzheimer and other dementia-related conditions. Considering relatives and caregivers among others, this means additional millions of people affected. Despite expansive research also on the impact on welfare and health-care systems, the question of dementia from a democratic perspective has been neglected thus far. However, the current situation and projected developments require us to reflect on how participation and inclusion are fundamentally challenged for citizens with dementia. Consequently, the following explores pressing theoretical implications and emerging democratic deficits for societies where, constrained by conventional forms of participation, a rapidly increasing number of citizens are excluded from political processes. Furthermore, as will be illustrated, non-conventional and participatory-oriented concepts could even exacerbate rather than ameliorate inclusion and participation. Finally, I further hope to prompt reflection on possible avenues to enhancing representation and inclusion, ensuring ‘vote and voice’ to an ever growing group of citizens.
This study examines how performing diaspora philanthropy in the country of origin (Morocco) and the experience of integration and inclusion in the country of residence (Netherlands) influences the sense of belonging amongst cross-border diasporic philanthropists. The examination combines theories on migration, cross-border diasporic philanthropy and the sense of belonging. Based on a qualitative exploration of the perspectives and motives of individual cross-border diasporic philanthropists (N = 30), the analysis reveals a profile of cross-border diasporic philanthropists for whom country of residence serves as a positive reference, due to the constant experience of inclusion. They use their country of residence as a reference for social change in their country of origin. This generates a sense of belonging amongst diasporic philanthropists. The findings of this study contribute to the existing literature on the sense of belonging within diasporic communities and cross-border diasporic philanthropists, thereby enhancing understanding of motivations for diasporic philanthropy.
Japan combines demographic challenges of decreasing childbirths and an ageing population, yet political unwillingness to use immigration to ease labour market and caregiving shortages. Paying attention to gender, diversity, and inclusion would seem to be a ‘rational’ political choice. Although Prime Minister Abe (Abe II) understands the need to appear to be responding to Japanese women qua equal citizens, women remain more an ‘object’ of LDP policy than a substantive beneficiary. To improve his image, Abe has incorporated ‘Womenomics’ into his strategy of economic revitalisation; the result has been a rather incoherent blend of ‘equal participation’ and ‘women’s utilisation’. In 2016, the dearth of diversity and anti-feminist sentiment within Japanese politics continues to be mirrored in both passive and active ways within the discursive and institutional political climate, including within academia. It is largely premature to assume a shared normative or scientific commitment to inclusion and diversity in Japan. Japanese Political Science (JPS) is no exception, and this has obvious implications for what constitutes a ‘serious’ political issue worthy of study, what gets funded, who gets hired, and the extent to which critical debates within feminist political science (FSP) on gender, race, and diversity are taken seriously. In this article, I offer a preliminary evaluation of JPS in light of three indicators: the under-representation of women in Japanese academia generally and political science specifically; the access of FPS to large-scale government funding grants (2003–2013) and its impact on the discipline; and recent efforts by feminist political scientists in Tokyo to create a ‘home’ for debates on gender, diversity, and political representation. I conclude with a hopeful expectation that increasing numbers of political scientists in Japan will begin to genuinely problematise the dearth of diversity in Japanese politics and to approach this fundamental puzzle of Japanese democratisation with the intellectual curiosity that it deserves.
In western capitalist societies the state has become increasingly criticized for its inadequacy as a mechanism for distributing welfare inclusively. In particular, it has been criticized for its lack of flexibility in meeting the needs of increasingly plural populations, and for being too distant to enable service users to participate in the meeting of their welfare needs. Consequently, in many countries, including the United Kingdom, voluntary and community associations have been used to distribute welfare with the belief that it can remedy the defects of universal state provision. This paper suggests the voluntary and community sector can only achieve this if the organizations are democratically organized, ensuring participation from staff and users. Moreover, participation should be based around the norms of deliberative democracy. The paper argues that this form of participation will best ensure that the needs, preferences, and interests of subordinate groups are included in social policy delivery, due to the fostering of public reason.
People with disabilities in the US are now a health disparities population. Though 25% of US adults have a disability, only 5% of medical research grants are disability related. Knowledge about researchers’ perceived barriers to including people with disabilities in research has focused on a single disability/condition and thus has limited translational science applications. Our CTSA’s Disability as Difference: Reducing Researcher Roadblocks (D2/R3) project examined such roadblocks towards inclusion of people with intellectual and developmental disabilities (I/DD). I/DDs are broad, heterogeneous conditions that originate in childhood, have varying impact and function, and persist throughout the lifespan. Strategies that mitigate their under-representation in research will likely have general applicability to all disabilities. In D2/R3’s first phase we conducted semi-structured interviews with translational science and I/DD program leaders at ten US institutions about perceived barriers and facilitators to including people with I/DD in research. Interviews were held with 25 individuals from partnering Intellectual and Developmental Disabilities Research Centers, University Centers for Excellence in Developmental Disabilities, and Clinical and Translational Science Award programs. Collaborative thematic coding identified key themes as: attitudinal barriers (e.g., assumptions about consent capacity), logistical barriers (e.g., accommodation costs), health disparities, and generalizability concerns. Findings informed development of a survey based on Prosci’s ADKAR® model of change management’s five components: Awareness, Desire, Knowledge, Ability and Reinforcement. Exclusion appears to stem from researchers’ lack of awareness, misconceptions, and knowledge gaps rather than insurmountable obstacles.
Selection processes in France are governed by a comprehensive legal and regulatory framework that prioritizes fairness, non-discrimination, and equal opportunity. French labor laws explicitly prohibit discrimination based on twenty-five criteria, including sex/gender, ethnicity, disability, and age. Despite these protections, disparities persist, fueling ongoing policy debates and legislative refinements. Regulatory bodies such as the Defender of Rights oversee compliance and promote unbiased hiring practices. However, implicit biases and structural barriers continue to influence employment decisions, challenging efforts to achieve true workplace equality. Employers must balance legal obligations, diversity objectives, and test validity while adapting to evolving EU regulations, such as the AI Act (2024). The introduction of diversity labels and corporate social responsibility initiatives reflects a proactive commitment to fostering inclusive workplaces. Yet enforcement challenges remain, as rising reports of workplace discrimination highlight persistent gaps. Several recommendations have been proposed to mitigate discrimination without compromising the quality and effectiveness of selection methods.
This chapter has been written from the stance of a patient and public contributor to mental health research. It examines the role of patient and public involvement in mental health research which has evolved since the mid 1960s and continues to do so. Examining the people, roles and research and providing a definition for the different stages of Patient and Public Involvement, the chapter looks at how these roles interact, the ethics and rationale for involvement, the power relations between the various parties, whether involvement is moving the research agenda closer to preventative health care, and the subject of equality, diversity and inclusion. The difficulties of working with people with serious mental health issues are addressed. Case studies are given to illustrate various points. Subjects such as training and language are included. The complex subject of evaluation and impact and how they can be resolved are raised. Finally, the chapter concludes by inviting the reader to consider what ‘good PPI’ is, and how it is done.
This textbook provides students with basic literacy on key issues related to Justice, Equity, Diversity, and Inclusion in the United States. Over twelve chapters, it employs critical race theory and intersectionality to promote critical thinking and civic engagement on issues such as American culture, gendered racism, and Black reparations. Each chapter employs interactive and engaging opportunities to learn, making it the ideal introductory resource for undergraduate students. The text is structured around real-world stories, which exemplify the humanity of each person and the complexity of these issues. Causadias presents questions for further discussion or to enhance comprehension, defines key concepts, debunks popular myths, summarizes evidence from trusted sources that challenge misinformation and disinformation, and proposes in-class exercises. Curated reading lists can be found at the end of every chapter for readers to expand their understanding of different topics. This book is also available as Open Access on Cambridge Core.