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The barefoot-doctor scheme in rural China during the Cultural Revolution of 1966–76 was a synonym for social medicine in the People’s Republic of China. This chapter examines how sociopolitical, disease, and economic factors contributed to the development of the barefoot-doctor program and shaped the unique path of social medicine in China. It analyzes how the government clarified and addressed the dilemma between ideological equity and structural inequity. Furthermore, it discusses how disease models both facilitated and challenged the barefoot-doctor program and impacted on social medicine, and investigates how the changing roles and function of barefoot doctors has impacted social medicine in the evolution of community medicine. The barefoot doctors echoed the themes of social medicine in developing and developed countries and left its inspirations and legacies. By revisiting the state’s role in the barefoot-doctor program, the chapter provides a new understanding of the global history of social medicine in the twentieth century and beyond.
Edited by
Richard Pinder, Imperial College of Science, Technology and Medicine, London,Christopher-James Harvey, Imperial College of Science, Technology and Medicine, London,Ellen Fallows, British Society of Lifestyle Medicine
Health inequalities refer to unfair and avoidable differences in health across populations, influenced by factors such as socio-economic status and societal inequality. These disparities are evident in various health and social outcomes, including child mortality, obesity, and life expectancy. Lifestyle Medicine, which focuses on individual behaviours, acknowledges the need for multi-level action to address health inequalities effectively. Strategies to improve health equity must consider individual circumstances, providing support according to specific needs. For instance, addressing food insecurity, promoting physical activity, and ensuring good quality sleep are Public Health targets that can benefit both individuals and society. Interventions must be tailored to overcome barriers such as cost, availability of resources, and safe environments for positive health behaviours. Ultimately, tackling lifestyle-related health inequality requires a collaborative effort between Lifestyle Medicine and Public Health, aiming for upstream changes to social determinants and advocating for a more equal society
This chapter argues that the implications of territorial disputes for individuals are seldom considered in the Court’s legal reasoning and proposes ways to do so. It first observes that the Court traditionally resolves territorial disputes with reference to a firm hierarchy of titles, few of which allow for the consideration of individuals. It then considers how the title of effectivités could potentially allow for the consideration of individuals and acknowledges that their rights and needs have been mentioned by the Court as an afterthought in certain judgments. It analyses the reasons for the Court’s approach and argues that the principle of equity could play a stronger role in allowing for the consideration of individuals in territorial disputes.
This chapter identifies the distinct contexts in maritime disputes where concerns for local populations are raised in states’ arguments but dismissed by the Court. It observes that the overarching reason underpinning this approach is the Court’s adherence to legal formalism. This approach is appropriate when determining the pre-existence of a maritime boundary before delimiting one. However, when adjusting a provisional line in maritime boundary delimitation, it argues that the principle of equity can play a greater role in promoting a fuller consideration of the needs of local populations. Beyond the delimitation process, when attributing sovereignty to a maritime zone, the dismissing concerns for local populations has taken the form of rejecting states’ arguments regarding historic fishing rights. In this context, this chapter argues that reframing the understanding of stability can allow for historic fishing rights to be upheld and, therefore, for the needs of local populations to be considered.
How can organizations better achieve inclusion, equity, and superior performance from diversity? Decades of stalled progress require a wider range of policies. Applying a system thinking approach to a transdisciplinary synthesis of research findings, the authors' comprehensive framework guides inquiry and practice by identifying problematic dynamics. Comparative case studies reveal, in contrast, favorable dynamics of intergroup contact that result from an evolved elaboration of practices for inclusive interactions, socialization, and accountability. Over time, when promoted for mission attainment, applied to all members, and customized to the workgroup, the practices generate inclusion, equity, and superior performance.
The concept of equity is indispensable to Kantian morality. This claim is controversial given Kant’s labelling of equity as an unenforceable right and his reputed moral absolutism. A need for equity, however, can be elicited from within his writing. For Kant, human dignity constitutes the basis of duty. Conscience demands conformity with duty. Our duties to positively serve humanity are indeterminate. The need for equity arises, therefore, to guide conscientious deliberations in applying moral principles appropriately toward that end in particular situations. This is especially pronounced when one strives to support the dignity of others consistently with one’s own dignity.
Colonialism has produced the global health system, and decoloniality must inform global health law. This article considers the foundational impact of colonialism on the global health system and advocates for adopting decoloniality as a crucial framework to reshape global health law. Through a historical lens, it examines how European colonialism established power dynamics and structures that continue to influence contemporary global health governance. This article calls for overcoming enduring challenges by emphasizing the urgency of dismantling outdated and unjust systems that perpetuate health inequities and hinder effective interventions. It argues for a paradigm shift toward epistemically inclusive, ethical, and equitable practices, emphasizing the active participation of marginalized communities in health policymaking. By addressing the root causes of health disparities and decoupling health systems from racial capitalism, a decolonial approach promises a more just and effective future for global health law.
The Damna Usuum was a series of complaints about the operation of uses written during the negotiations with the Commons which culminated in the Statute of Uses (1536). Through detailed analysis of the manuscript, this paper demonstrates that the Damna Usuum has been misunderstood by legal historians. Rather than being a public document intended to persuade the Commons to support reform; the Damna Usuum can be shown to be a series of rough notes prepared by the Crown’s lawyers ahead of their negotiations with the Commons. Furthermore, this has a significant impact on our understanding of how contemporary lawyers conceptualised pre-1536 uses in a period in which they had taken on more proprietary “thing-like” characteristics.
This chapter examines the challenges in measuring long-term care needs to determine eligibility and the impact of eligibility rules on access to care and wellbeing, focusing on European countries with established long-term care systems. Eligibility rules are crucial for identifying individuals with the greatest need and ensuring equitable resource distribution, yet defining these rules is challenging due to the lack of a universal approach to measuring health and social needs. Consequently, some individuals with functional or cognitive limitations may be inadequately supported or face high out-of-pocket costs, leading to reliance on informal care or unmet needs. This can reduce their independence and increase the risk of costly hospitalizations. The chapter advocates for expanding eligibility rules to improve coverage, equity, and efficiency, highlighting their role in increasing access to care, reducing poverty due to care costs, and enhancing wellbeing.
This chapter concludes by summarizing the evidence presented in the book and considering the way forward by re-visiting the arguments in favour of investing in long-term care and the costs of inaction.
Conventional benefit–cost analysis plays an important role in informing policy decisions, encouraging systematic investigation of the positive and negative impacts of alternative policies. It is based on strong normative assumptions, however. To measure individual wellbeing, the conventional approach relies on individuals’ willingness to exchange their income for the outcomes they experience. To measure societal welfare, it relies on simple aggregation of these values across individuals. In this “Ethics and Benefit–Cost Analysis” special issue, we explore alternative conceptions of individual and societal welfare, their application, and the implications, from both practical and ethical perspectives.
Community advisory boards (CABs) have traditionally been formed in the context of discrete projects and served to support community protections within the confines of the associated investigation(s). However, as funding bodies increasingly prioritize health equity, CABs have shifted – evolving into long-running organizations with broader scope and value. An emerging cornerstone of these project-independent boards (PICABs) has been the formation of “Research Review Boards” (RRBs). While unified in their goal of promoting community protection and representation in health research, it is unknown to what degree RRBs differ on key features including membership, leadership, service reach, and – crucially – impact. A scoping review was conducted according to PRISMA-ScR guidelines to analyze current practices for RRBs. Of screened articles (n= 1878), 25 were included, corresponding to 24 unique RRBs. Findings indicated overlaps in the stated missions, funding structures, and processes of most RRBs. Differences in membership composition, location, service-reach, leadership structures, evaluation procedures, and perceived impact were evident. Where data is available, RRBs receive positive endorsement from both internal members and external users. Standardization of evaluation procedures is needed to fully quantify impact. Additional challenges to sustainability, communication, and conflicts (e.g., of interest, commitment, and power differentials) merit further consideration.
This chapter discusses multicultural humanistic psychology, which is a theoretical foundation that seeks to engage the culturally relative self-actualization processes of the individual and community through the diverse spectrum of multicultural facets, so that wellbeing and social and emotional intelligences flourish. This paradigm synthesizes the strengths of both humanistic psychology and multicultural paradigms to support clinicians and educators in engaging with phenomena in the rapidly changing world. Multicultural humanistic psychology is not about validating Western cultural paradigms so that a new theory can be prepackaged and distributed globally. Rather, it is a way to awaken the potential of consilience, to recognize and transcend limitations, and acknowledge that together the fields are more relevant to global challenges. This paradigm guides the further discussions on social and emotional intelligences.
The diversity gap in precision medicine research (PMR) participation has led to efforts to boost the inclusion of underrepresented populations. Yet our prior research shows that study teams need greater support to identify key decision-making issues that influence diversity and equity, weigh competing interests and tradeoffs, and make informed research choices. We therefore developed a Diversity Decision Map (DDM) to support the identification of and dialogue about study practices that impact diversity, inclusion, and equity.
Methods:
The DDM is empirically derived from a qualitative project that included a content analysis of documents, observations of research activities, and interviews with PMR stakeholders. We identified activities that influenced diversity goals and created a visual display of decision-making nodes, their upstream precedents, and downstream consequences. To assess the potential utility of the DDM, we conducted engagements with stakeholder groups (regulatory advisors, researchers, and community advisors).
Results:
These engagements indicated that the DDM helped diverse stakeholder groups trace tradeoffs of different study choices for diversity, inclusion, and equity, and suggest paths forward. Stakeholders agreed that the DDM could facilitate discussion of tradeoffs and decision-making about research resources and practices that impact diversity. Stakeholders felt that different groups could use the DDM to raise questions and dilemmas with each other, and shared suggestions to increase the utility of the DDM.
Conclusion:
Based on a research life course perspective, and real-world research experiences, we developed a tool to make transparent the tradeoffs of research decisions for diversity, inclusion, and equity in PMR.
We use a within-subject experimental design to investigate whether systematic relationships exist across distinct features of individual preferences: altruism in a two-person context, risk aversion in monetary outcomes, and social preferences in a group context. We find that altruism is related to demographic variables, including years of education, gender, and age. Perhaps most importantly, self allocation in a two-person dictator game is related to social preferences in a group context. Participants who are more generous in a dictator game are more likely to vote against their self-interest in a group tax redistribution game which we interpret to be an expression of social preferences.
An inequality game is an asymmetric 2 × 2 coordination game in which player 1 earns a substantially higher payoff than player 2 except in the inefficient Nash equilibrium (NE). The two players may have either common or conflicting interests over the two NE. This paper studies a redistribution scheme which allows the players to voluntarily transfer their payoffs after the play of an inequality game. We find that the redistribution scheme induces positive transfer from player 1 to player 2 in both common- and conflicting- interest games, and is particularly effective in increasing efficient coordination and reducing coordination failures in conflicting-interest games. We explain these findings by considering reciprocity by player 1 in response to the sacrifice made by player 2 in achieving efficient coordination in conflicting-interest games.
Though Health Technology Assessment (HTA) has steadily grown over the past decades, less attention has been paid to the way HTA may prove more responsive to the broader economic, social, and environmental challenges that health systems are facing today. In view of climate change, chronic diseases, an aging population, inequalities, and workforce issues, the HTA community’s unique set of skills nonetheless holds great potential to help decision-makers strengthen many publicly funded health systems around the world.
Methods
This article adopts an integrated system-wide perspective guided by the Responsible Innovation in Health (RIH) framework to explore how the HTA community may not only adapt to the speed of innovation but also consider its direction.
Results
Because RIH aims to steer innovation toward a more sustainable pathway, it can help HTA agencies anticipate decision-makers’ informational needs regarding four systemic challenges: (1) equitable access; (2) workforce issues; (3) accountable policy trade-offs; and (4) environmental sustainability. We clarify how key elements of the RIH framework may be used by HTA agencies to: (1) supplement their evaluation process; (2) align their priority-setting or strategic planning activities with their health system challenges; or (3) inform the production of early HTAs, horizon scans, or reports that are broader in scope than a single technology review.
Conclusions
The article concludes with three practical implications that were identified by the Institut National d’Excellence en Santé et Services Sociaux (INESSS) (Québec, Canada) and may inspire other HTA agencies.
Childhood morbidity is a precursor and contributor to under-five child mortality. Community-based primary healthcare programs are culturally responsive and low-cost strategies for delivering maternal and child health services in rural communities.
Aim:
To evaluate the equity effect of the Ghana Essential Health Intervention Program (GEHIP) – a five-year community-based primary healthcare program – on childhood morbidity.
Methods:
GEHIP was implemented in the Upper East region of Northern Ghana. Household baseline and end line surveys conducted in 2010/2011 and 2014/2015, respectively, from both intervention and comparison districts were used to assess three childhood morbidity conditions: maternal recall of neonatal illness, the incidence of diarrhoea, and fever. Difference-in-differences analysis, mean comparison test, and multivariate logistic regressions are used to assess the effect of GEHIP exposure on these three childhood morbidity conditions.
Results:
Baseline sample data of 2,911 women and end line sample of 2,829 women were included in this analysis. There was generally more reduction in all three childhood morbidity conditions in intervention communities relative to comparison communities. Diarrhoea and fever had a statistically significant treatment effect (AOR = 0.95, p-value<0.01 and AOR = 0.94, p-value<0.001). Results of equity analysis indicate significant mean reductions for both the poor and non-poor for neonatal illness and diarrhea, while only the intervention group had a significant reduction for both poor and non-poor for fever. Regression analysis shows no significant equity/inequity effects of GEHIP on the incidence of diarrhoea and fever. Neonatal illness, however, shows significant effects of wealth within the intervention group.
Conclusion:
This study shows that GEHIP contributed significantly to childhood morbidity reduction. This implies that community-based strategies have the potential to improve child health and contribute to the attainment of the United Nations sustainable development goal related to child health. Specific targeted measures are recommended to ensure both the poor and relatively better-off benefit from interventions.
In recent years, there has been a growth in awareness of the importance of equity and community engagement in clinical and translational research. One key limitation of most training programs is that they focus on change at the individual level. While this is important, such an approach is not sufficient to address systemic inequities built into the norms of clinical and translational research. Therefore, it is necessary to provide training that addresses changing scientific norms and culture to ensure inclusivity and health equity in translational research.
Method:
We developed, implemented, and assessed a training course that addressed how research norms are based on histories and legacies of white supremacy, colonialism, and patriarchy, ultimately leading to unintentional exclusionary and biased practices in research. Additionally, the course provides resources for trainees to build skills in how to redress this issue and improve the quality and impact of clinical and translational research. In 2022 and 2023, the course was offered to cohorts of pre and postdoctoral scholars in clinical and translational research at a premier health research Institution.
Results:
The efficacy and immediate impact of three training modules, based on community engagement, racial diversity in clinical trials, and cancer clusters, were evaluated with data from both participant feedback and assessment from the authors. TL1 scholars indicated increased new knowledge in the field and described potential future actions to integrate community voices in their own research program.
Conclusions:
Results indicate that trainings offered new perspectives and knowledge to the scholars.
Ensuring more equitable transformations requires addressing how different contextual dimensions of identity, such as gender and class, hinder equity. However, previous analyses on equity have addressed these dimensions separately. We suggest advancing beyond these methods by integrating intersectional analysis into the distributive, procedural, and recognition aspects of equity when examining social–ecological transformations. A review of 37 studies on social–ecological transformation shows that social–ecological transformation scholars commonly addressed social, spatial, and environmental transformations. In contrast, few studies have gone into depth in analyzing the reasons for power imbalances. We encourage scholars to use critical questions to reflect on social–ecological transformations collectively.
Technical summary
Ensuring equity in social–ecological transformations involves understanding how aspects of identity – such as gender, age, and class – affect experiences on the path to sustainability. Previous studies have often focused on one dimension of difference, but an intersectionality framework is essential for recognizing interconnected identities. In this paper, we review 37 empirical studies on social–ecological transformations, identifying key assets of transformation, including economic, social, cultural, political, spatial, environmental, and knowledge-based assets. We apply an analytical framework based on intersectional equity, incorporating intersectionality in equity analysis, which examines how power dynamics contribute to inequities in distribution, procedure, and recognition. Our findings show that social, spatial, and environmental assets of transformation are the most frequently mentioned in our sampled literature, together with benefits, costs, inclusiveness, and knowledge of equity dimensions. Power imbalances occurred the most often, while different aspects of identity were mentioned only in two-thirds of the studies. We believe an intersectional equity approach will help better conceptualize transformation concerning (in)equity. Based on our reflections, we suggest critical questions encouraging scholars to evaluate them iteratively with an interdisciplinary group.
Social media summary
An intersectional equity approach is key to just social–ecological transformations. We review 37 studies to show why.