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Demand for child and adolescent mental health support is rising, with long waits risking deterioration. The Lucy Project provides rapid, self–referral, low–intensity CBT (LICBT) within paediatric settings, with interventions taking place via video call. While previous work suggests good reach and outcomes, equity of access and acceptability across demographic groups requires evaluation. This paper examines whether socioeconomic status (SES) and ethnicity are associated with engagement with the service. Service records for 149 patients referred to The Lucy Project in Sheffield Children’s Hospital between December 2022 and December 2024 were analysed. Engagement (engaged vs not–engaged) was recorded, and this was analysed in the context of ethnicity (White British; other; unknown) and indices of multiple deprivation (IMD) decile. Binary logistic regression tested associations. The sample’s ethnicity was broadly similar to that of the general population where the service is based; 27.5% lived in the two most deprived IMD deciles (vs 34.2% citywide). Ethnicity did not predict engagement, whereas IMD decile was shown to be associated with engagement. Results suggested that the more affluent a patient, the more likely they were to drop out. In this video-based, self–referral LICBT service, engagement did not differ by ethnicity but was higher among children and young people from more deprived areas. Findings support the model’s potential to mitigate socioeconomic barriers post–referral, while highlighting the need to optimise engagement for more affluent families and to continue addressing pre–referral inequities and digital exclusion.
Key learning aims
(1) To Understand the context of the implementation of The Lucy Project, a self-referral low-intensity cognitive behavioural therapy service in a paediatric setting.
(2) To explore the relationship between experiences of deprivation and its impact on engagement with The Lucy Project.
(3) To explore the relationships between ethnicity and engagement with The Lucy Project.
(4) To explore potential pros and cons of a self-referral mental health service in a paediatric setting.
This chapter addresses three questions about health systems: What is a health system? What are health systems for? What functions should a health system perform? A health system can be understood as an interconnected set of structural relationships between two components: a population and a set of providers. A health system includes the resources, actors and institutions related to the financing, regulation and provision of activities, whose primary intent is to improve or maintain health. Health systems include personal health services, hybrid health services and population health services. The defining purpose of the health system is to improve health, both the average level and its distribution across individuals. Two other intrinsic goals of the health system should be responsiveness to the legitimate expectations of the population, and fairness in financial contribution. Health systems must perform five basic functions: financing, provision, resource development, systemic integration and the meta-function of stewardship.
Conventional service design methods are valuable for improving healthcare experience, but are limited in scale and information capture. Based on a constructed database of 2,320 stories from patients and carers with multiple long-term conditions (MLTC), this paper shows how real-life experiences can be used to inform healthcare service redesign. By combining the richness of qualitative insight with the breadth and representativeness of large-scale data, it identifies “Continuity of care”, “Care coordination”, and “Temporal – Access to services” as the priority redesign opportunities for MLTC.
Nadheim offers healthcare to persons selling sexual services. Using relational, feminist, and system-oriented design, a rich design methodology combined cultural probes, vignette studies, and giga mapping unc toovered issues of service fragmentation, stigma, and digital exclusion. A co-created digital tool offering anonymous, centralized access to health, legal, and support services. An added speculative concept imagines a sex worker union to allow for radical change. Findings highlight trust, inclusion, and co-agency, positioning design as a catalyst for social justice.
This paper explores the role of artificial intelligence to reduce resource burden and support service delivery processes in generalist secondary-care mental health services in the Netherlands. Through semi-structured interviews with domain experts and using service blueprinting as a stimulus, we identified challenges and bottlenecks in mental health care pathways and intervention opportunities. We propose four intervention directions for design researchers and developers to prototype and assess how AI technologies may alleviate capacity issues in mental healthcare.
Nurses and midwives must be able to provide culturally safe health care to all Aboriginal and Torres Strait Islander peoples. Yatdjuligin: Aboriginal and Torres Strait Islander Nursing and Midwifery Care introduces readers to historical and contemporary approaches to Indigenous nurse-led theory, research and praxis. Now in its fourth edition, Yatdjuligin advocates for the knowledge and experiences of First Nations peoples to be prioritised across all health care contexts. New chapters on healthcare in custodial care settings, long-term health conditions and the effects of climate change on Indigenous people's health have been added. Updated case studies and reflective questions offer students realistic examples of theory in practice, encouraging them to consider and challenge their own beliefs and understandings. Written entirely by leading Aboriginal and Torres Strait Islander nurses, midwives, academics and researchers, Yatdjuligin is an essential resource for students establishing the foundations of culturally safe healthcare in their practice.
This chapter offers an historical examination of Aboriginal and Torres Strait Islander healthcare from a nursing viewpoint. It considers how the current shape of Aboriginal and Torres Strait Islander health has been formed by actions taken since European colonisation. It discusses the status of Aboriginal and Torres Strait Islander health during different historical periods, including what is known about the pre-invasion health system and health service provision during the periods of initial contact, separation and protection. Finally, the chapter discusses the rise of the Aboriginal and Torres Strait Islander community-controlled health system and contemporary choices for Aboriginal and Torres Strait Islander people in the delivery of healthcare and health outcomes. It further discusses the approach taken by all Australian governments of working with Aboriginal and Torres Strait Islander people, communities and organisations to implement the new National Agreement on Closing the Gap at the national, state and territory, and local levels. Each section of this chapter is framed within the prism of nursing, exploring the role of nursing in health systems and the delivery of healthcare.
In this facility-based cross-sectional survey in primary health care centres in southern Ethiopia, women attending for antenatal care (ANC) were screened for depression (PHQ-9; score ≥ 5 and functionally impaired), anxiety symptoms (GAD-7; score ≥ 10), post-traumatic stress disorder (PCL-5 score ≥ 31), intimate partner violence (IPV; non-graphic language screening test) and risky substance use (ASSIST). Clinical notes were reviewed post-consultation for evidence of health worker recognition of psychosocial concerns and actions taken. Of the 2,079 interviewed women, 24.9% had at least one psychosocial problem, and 7.3% had two or more. The most common psychosocial problem was probable IPV (n = 289; 13.9%, 95% CI: [12.57–15.25]), followed by risky khat use (n = 134; 6.5%, 95% CI: [3.72–10.94]) and depression (n = 110; 5.3%, 95% CI: [3.98–7.00]). Identification by ANC professionals was low: 2.7% of women with probable depression, none with probable IPV had it recorded. A history of mental health problems was not documented in 99.7% and only 47.3% (n = 938) reported being asked how they were feeling emotionally. Systemic changes to provider training and procedures are required to promote person-centred maternal care and improve identification of psychosocial problems in ANC in rural Ethiopia.
This chapter examines how medical workplaces – as material places and as institutions - protect or undermine the physical and emotional lives of the doctors who work there. Workplaces include hospitals, ambulatory clinics, locum settings, and precarious workplaces such as international humanitarian medical work, and newer, non-material workplaces such as telemedicine. Dominance and sexual harassment can occur in the interstices of all these workplaces, and sometimes in the full view of others.
Sexual harassment not only harms survivors; it also has impacts on the team, the organisation and the profession. Harms can include changes in the way teams and individuals interact, which can have a direct impact on the quality of patient care. It can mean survivors and witnesses are less able to be empathic and interpersonally aware, as they are focussed on defensive and protective behaviours. Sexual harassment by a senior colleague changes the way survivors and bystanders see their profession, and this can cause long-lasting harm in their own practice. Many survivors leave or change their workplace, causing workforce deficits and loss of experience and skills. Those survivors who live with intersectional disprivilege provide critical diversity in teams that need to manage a breadth of patient experience. Unfortunately, they are at higher risk of sexual harassment, and so are more likely to leave, restricting the profession’s capacity to respond to community needs across the breadth of the population. The cost is a drop in the capacity of the organisation to provide quality care.
This chapter defines sexual harassment and its key targets and perpetrators to argue that their attitudes and beliefs are the anthesis of medical values and principles – to do not harm. It identifies the costs to the organisations of this sexual harassment and abuse. Adopting a preventative medicine framework we extend the scale and focus of prior work to consider evidence-based SHA interventions. We aim to advance current understanding about SHA and its detection, deterrence and amelioration within the health workforce through a multi-level and multi-stage SHA prevention strategy that collectively impacts up- and down-stream changes for this workforce and their workplaces. We outline five levels at which awareness raising, education and intervention is required – to include primordial, primary, secondary, tertiary, and quaternary.
This chapter describes the role of medical regulators including the history of the International Association of Medical Regulatory Authorities (IAMRA). It highlights the common key processes of medical regulation agencies internationally and the standards of practice that are relevant to sexual harassment and abuse of doctors by doctors.
Examples of regulatory standards specifically relevant to sexual harassment and abuse of are drawn from the regulatory frameworks of several different countries illustrating the range which varies from specifically condemning sexual harassment to more generic requirements for good behaviour, productive and respectful collegiality and being aware of power imbalances.
In the final section the author documents typical regulatory processes that occur on receipt of a complaint of sexual harassment or abuse by a doctor as well as the range of responses that may occur if an adverse finding is made against a doctor. The advantage of involving medical regulators is that it allows communication about concern regarding perpetrators found to have failed the standard between jurisdictions and between specific clinical settings.
This chapter discusses the role of men in abuse of doctors by doctors. The chapter considers the role of men at all levels including victim, bystander, perpetrator, employer or those within the regulatory and legal systems. The chapter helps us to understand and look beneath the obvious drawing on the evidence of men’s roles at all levels. It also speaks to the potential of men to positively influence for change and prevention of abuse, as well as drawing our attention to possible risks of abuse occurring. It raises our awareness of the ‘not so innocent bystander’ and the significant potential of engaging bystanders, colleagues, and system leaders into positive action.
This chapter introduces the potential legal consequences of occupational sexual harm of medical practitioners by medical practitioners, and outlines some of the reasons for non-reporting in the criminal context. The challenges of reporting of sexual harm in the workplace are discussed and followed by three illustrative case studies from Australia one from a criminal court, one from a civil court and one case brought by the Medical Board to the Administrative Appeals Tribunal. The chapter concludes with the recognition that complex structural and cultural environments exist which deter some victims from pursuing legal redress and can inadvertently harm those who do pursue it. Solutions are not simple or easy and, irrespective of the prevalence of occupational sexual harm, pursuit of legal claims is likely to remain low due to the personal and professional risks a complainant endures.
This chapter draws from work and social-cognitive psychology, which is concerned with understanding people at work, and specifically the social and individual cognitive dimensions to these serious misconducts. It offers a distinct perspective on sexual harm, by focusing on three interconnected elements: the individual, the specific types of behaviours, and the environment. Understanding these distinct elements and how they combine, alongside insight into different inhibitors is critical not only understanding why these events occur, but also why they persist. This lens highlights the role of power and its abuse by elites, and why others may be reluctant to challenge and raise their concerns. It also reveals why a professional, undertaking morally praiseworthy activities may paradoxically be more at risk from the distorting cognitive processes of moral licensing. Psychology offers new perspectives into these phenomena and more critically into upstream preventative responses, to show why remediative sanctions may not be so simple here.
The framework of human rights has permeated international discourse and has evolved into standards that are replicated at international, regional, and domestic levels. This chapter utilises the human rights framework to explore the value it may offer in addressing the issue of abuse between medical practitioners. Beginning with a brief description of the overarching instruments from which the modern understanding of human rights stem, the chapter progresses to look at the specific human rights instruments at an international, regional, and domestic level. This analysis concludes the human rights framework offers little to an individual in terms of timely redress, however, the value of this approach lies in collective advocacy. Utilising a common language, global criteria, and data, human rights act as a point of agitation which can assist in exposing archaic notions around appropriate workplace behaviours and transforming rights into enshrined legislative materials with the full protection of the law. The human rights framework should be pursued alongside a more responsive methodology, such as though legal options and mechanisms, until such a time as neither are required.
Sexual harassment between doctors is a common problem hiding in plain sight. There have been prevalence studies across the world, across contexts and across disciplines and although definitions,methodologies and results vary, the prevalence of sexual harassment inmedicine continues to be unacceptedly high.Harassment is more common when the survivor is still in training, and it is more likely to be experienced by doctors who live with multiple marginalisations. This book combines expert analysis and commentary from multiple interdisciplinary perspectives. It privileges the voices of survivors, whose rich experience helps to inform our understanding of a complex problem. With contributing authors from Austria to Zambia, the book spans multiple languages, sociocultural contexts, and academic disciplines and offers unique globally contextualised perspectives. It gives leaders, scholars and survivors a nuanced, holistic understanding of sexual harms between doctors, and it demonstrates how silence prevents effective evidence-based management of sexual harassment. This volume not only helps to break the silence, it also offers potential solutions in discrete cultural contexts. This title is also available as Open Access on Cambridge Core.
Perinatal mental health disorders are prevalent in Ecuador and Peru. Despite national health policies supporting maternal mental health care, service provision remains fragmented, relying on a mix of public, private, and nongovernmental actors. This study examined professional interest holders’ perceptions of barriers to perinatal mental health care and the solutions they propose. We employed a mixed-methods approach. First, a systematic review of publicly available data was conducted to identify organizations engaged in maternal and mental health care in Ecuador and Peru. Following this, in-depth, semistructured interviews were conducted with 17 key informants representing research institutions, nongovernmental organizations (NGOs), government agencies, and private sector entities. Thematic analysis was applied to identify structural barriers, institutional challenges, and proposed solutions. Findings revealed multilevel barriers to perinatal mental health care, including stigma, financial constraints, limited provider training, fragmented health services, and bureaucratic inefficiencies. Community-based interventions, task-shifting strategies, and increased public education were identified as effective approaches to addressing these challenges. Participants also emphasized the need for intersectoral collaboration, increased governmental investment, and policy reforms to strengthen maternal mental health services. Efforts to improve perinatal mental health care in Ecuador and Peru require a combination of culturally sensitive, community-driven interventions, as well as sustainable government investment and commitment.
Critical to successful engagement in any organisation is an understanding of the important elements affecting good communication. There are many dimensions to the study of communication in the 21st century, both generally and in health service settings, in the 21st century. This chapter considers the foundational concepts, with references to help students discover more about communication in organisational, social and cultural settings. Many believe that even the definition of communication is worth questioning. As a notion it is so discursive and diverse that any definition other than the simplest becomes so complex as to cease being useful.
Intense debate surrounds the differences between the roles, functions and even the differences between leaders and managers. Leadership is not wholly different from management; indeed, it is a component of management and a responsibility of management, especially of senior managers. Effective managers need to be effective leaders, and the most effective leaders are also good managers.