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Stacy M Carter

Biographic Data

ID189982
NAMEStacy M Carter
GIVEN NAMESStacy M
FAMILY NAMECarter
SIGNATURECARTER S M
AFFILIATIONSThe University of Sydney
ORCID0000-0003-2617-8694
VERIFIEDYes
TOTAL WORKS59
TOTAL CITATIONS82
AUTHOR COUNT59
EDITOR COUNT0
FIRST PUBLICATION YEAR2001
LATEST PUBLICATION YEAR2026
H-INDEX7
  • Towards Evidence of Rigour in Empirical Deliberative Democratic Methods: Development and Piloting of the C‐JuRI Framework

    Open Access•Emma K Frost, Yves Saint James Aquino et al.•ARTICLE•Health Expectations•2026

    BACKGROUND: Deliberative democratic methods are increasingly being used to involve the public in health policy decision-making. These methods are rooted in deliberative democratic theory, which proposes the methods as democratic, inclusive and relevant ways to involve the public in policy decisions. Many practitioners have created methods for evaluating aspects of deliberative democratic engagement, but there are few practical guidelines for eval…

  • A critical analysis of the Australian public consultation on childhood vaccine mandate introduction

    Open Access•Sayali Gore, Katie Attwell et al.•ARTICLE•Social Science & Medicine•2026

    Several countries have revised their policies to make vaccine refusal more difficult. The role of the public in this process has seldom been examined. We analysed the public consultation process for the Australian government’s 2016 ‘No Jab No Pay’ mandatory childhood vaccination policy to better understand who participated, their arguments, and how their contributions were incorporated into the legislative process. Publicly available submissions …

  • Practical, epistemic and normative implications of algorithmic bias in healthcare artificial intelligence: A qualitative study of multidisciplinary expert perspectives

    Open Access•Yves Saint James Aquino, Stacy M Carter et al.•ARTICLE•Journal of Medical Ethics•2025

    BACKGROUND: There is a growing concern about artificial intelligence (AI) applications in healthcare that can disadvantage already under-represented and marginalised groups (eg, based on gender or race). OBJECTIVES: Our objectives are to canvas the range of strategies stakeholders endorse in attempting to mitigate algorithmic bias, and to consider the ethical question of responsibility for algorithmic bias. METHODOLOGY: The study involves in-dept…

  • Understanding Public Judgements on Artificial Intelligence in Healthcare: Dialogue Group Findings From Australia

    Open Access•Emma K Frost, Yves Saint James Aquino et al.•ARTICLE•Health Expectations•2025

    INTRODUCTION: There is a rapidly increasing number of applications of healthcare artificial intelligence (HCAI). Alongside this, a new field of research is investigating public support for HCAI. We conducted a study to identify the conditions on Australians' support for HCAI, with an emphasis on identifying the instances where using AI in healthcare systems was seen as acceptable or unacceptable. METHODS: We conducted eight dialogue groups with 4…

  • Making recommendations to subsidize new health technologies in Australia: A qualitative study of decision-makers’ perspectives on committee processes

    Open Access•Marcus Sellars, Stacy M Carter et al.•ARTICLE•Health Policy•2024

    OBJECTIVES: To explore experiences of, and perspectives on, health technology assessment (HTA) processes used to produce recommendations about subsidizing new medicines, and medical technologies in Australia, from the perspectives of those experienced in these processes. METHODS: Semi-structured interviews with a diverse group of 18 informants currently or previously members of the Pharmaceutical Benefits Advisory Committee (PBAC) or the Medical …

  • Accounts of harm and conflicts of interest in transvaginal mesh: Professional evaluations during an Australian Senate Inquiry

    Open Access•Mina Motamedi, Chris Degeling et al.•ARTICLE•SSM - Qualitative Research in…•2024

    Transvaginal mesh (TVM) surgeries were introduced as an innovative treatment for stress urine incontinency (SUI) and/or pelvic organ prolapse (POP) in 1996. Years after rapid adoption of these surgeries into practice, it emerged that TVM-associated adverse events were uncommon but potentially severe. This initiated global action, including an Australian Commonwealth Government Senate Inquiry, in 2017. This inquiry was both a causal factor in, and…

  • Public values to guide childhood vaccination mandates: A report on four Australian community juries

    Open Access•Chris Degeling, Julie Leask et al.•ARTICLE•Health Expectations•2024

    OBJECTIVE: Governments use vaccination mandates, of different degrees of coerciveness, to encourage or require childhood vaccination. We elicited the views of well-informed community members on the public acceptability of using childhood vaccination mandates in Australia. METHODS: Four community juries were conducted in Canberra, Launceston, Cairns and Melbourne, Australia between 2021 and 2022. We recruited 51 participants from diverse backgroun…

  • Transvaginal mesh in Australia: An analysis of news media reporting from 1996 to 2021

    Open Access•Mina Motamedi, Stacy M Carter et al.•ARTICLE•Health Expectations•2023

    INTRODUCTION: Transvaginal mesh (mesh) surgeries have been used to treat stress urinary incontinence (incontinence) and/or pelvic organ prolapse (prolapse). In Australia, as in many other countries, the harms caused by mesh eventually prompted individual and collective attempts to achieve redress. The rise of mesh surgery as a procedure, the experience of mesh-affected women and the formal inquiries and legal actions that followed all occurred in…

  • Multi-stakeholder preferences for the use of artificial intelligence in healthcare: A systematic review and thematic analysis

    Open Access•Vinh Vo, Gang Chen et al.•ARTICLE•Social Science & Medicine•2023

  • Reports of new healthcare AI interventions should include systematic ethical evaluations

    Open Access•William Rogers, Hal Draper et al.•ARTICLE•Bioethics•2022

  • Reimagining consumer involvement: Resilient system indicators in the Covid‐19 pandemic response in New South Wales, Australia

    Open Access•Patti Shih, Laila Hallam et al.•ARTICLE•Health Expectations•2022

    BACKGROUND: Reflections on the response to the COVID-19 pandemic often evoke the concept of 'resilience' to describe the way health systems adjusted and adapted their functions to withstand the disturbance of a crisis, and in some cases, improve and transform in its wake. Drawing from this, this study focuses on the role of consumer representatives in healthcare services in initiating changes to the way they participated in the pandemic response …

  • ‘Get your own house in order’: Qualitative dialogue groups with nonvaccinating parents on how measles outbreaks in their community should be managed

    Open Access•Kerrie Wiley, Penelope Robinson et al.•ARTICLE•Health Expectations•2022

    OBJECTIVE: Communities with high levels of vaccine rejection present unique challenges to vaccine-preventable disease outbreak management. We sought perspectives of nonvaccinating parents to inform public health responses in such communities. METHODS: Nineteen purposively sampled nonvaccinating Australian parents participated in one of seven online dialogue groups. We asked what they thought parents, school principals and public health profession…

  • Sharing precision medicine data with private industry: Outcomes of a citizens' jury in Singapore

    Open Access•Angela Ballantyne, Tamra Lysaght et al.•ARTICLE•Big Data & Society•2022•Cited by: 1•References: 33

    Precision medicine is an emerging approach to treatment and disease prevention that relies on linkages between very large datasets of health information that is shared amongst researchers and health professionals. While studies suggest broad support for sharing precision medicine data with researchers at publicly funded institutions, there is reluctance to share health information with private industry for research and development. As the private…

  • Direct-to-consumer detection of atrial fibrillation in a smartwatch electrocardiogram: Medical overuse, medicalisation and the experience of consumers

    Open Access•Patti Shih, Kathleen Prokopovich et al.•ARTICLE•Social Science & Medicine•2022•Cited by: 2•References: 31

  • Evaluation of artificial intelligence clinical applications: Detailed case analyses show value of healthcare ethics approach in identifying patient care issues

    Open Access•William Rogers, Hal Draper et al.•ARTICLE•Bioethics•2021

    This paper is one of the first to analyse the ethical implications of specific healthcare artificial intelligence (AI) applications, and the first to provide a detailed analysis of AI‐based systems for clinical decision support. AI is increasingly being deployed across multiple domains. In response, a plethora of ethical guidelines and principles for general AI use have been published, with some convergence about which ethical concepts are releva…

  • Sharing administrative health data with private industry: A report on two citizens' juries

    Open Access•Jackie Street, Belinda Fabrianesi et al.•ARTICLE•Health Expectations•2021

    BACKGROUND: There is good evidence of both community support for sharing public sector administrative health data in the public interest and concern about data security, misuse and loss of control over health information, particularly if private sector organizations are the data recipients. To date, there is little research describing the perspectives of informed community members on private sector use of public health data and, particularly, on …

  • Why Does Cancer Screening Persist Despite the Potential to Harm

    Open Access•Stacy M Carter•ARTICLE•Science Technology and Society•2021

    Population screening for early-stage cancer or cancer precursors began in the mid-twentieth century, with the goal of reducing suffering from cancer illness and lengthening average life by preventing cancer deaths. Since the establishment of cancer screening, concerns have emerged that it may be doing considerable harm; despite this, screening practices have remained relatively intractable. This intractability in the face of harm is the central p…

  • Stigmatized for standing up for my child: A qualitative study of non-vaccinating parents in Australia

    Open Access•Kerrie Wiley, Julie Leask et al.•ARTICLE•SSM - Population Health•2021

    Non-vaccinating Australian parents feel stigmatized for defending their child from perceived risk of harm, reporting a range of social and psychological effects, as well as financial effects from policies which disadvantaged their children through differential financial treatment, and diminished early childhood educational opportunities. While it might be argued that social stigma and exclusionary policies directed a small minority for the greate…

  • How do people understand overtesting and overdiagnosis? Systematic review and meta-synthesis of qualitative research

    Open Access•Tomas Rozbroj, Romi Haas et al.•ARTICLE•Social Science & Medicine•2021

  • Labels matter: Use and non-use of 'anti-vax' framing in Australian media discourse 2008-2018

    Open Access•Jay Court, Stacy M Carter et al.•ARTICLE•Social Science & Medicine•2021•Cited by: 8•References: 28

  • Methodological challenges in deliberative empirical ethics

    Stacy M Carter•ARTICLE•Journal of Medical Ethics•2020

    The abstract for this item has not been populated

  • Perspectives of Vietnamese, Sudanese and South Sudanese immigrants on targeting migrant communities for latent tuberculosis screening and treatment in low‐incidence settings: A report on two Victorian…

    Open Access•Chris Degeling, Stacy M Carter et al.•ARTICLE•Health Expectations•2020

    BACKGROUND: Tuberculosis (TB) elimination strategies in Australia require a focus on groups who are at highest risk of TB infection, such as immigrants from high-burden settings. Understanding attitudes to different strategies for latent TB infection (LTBI) screening and treatment is an important element of justifiable elimination strategies. METHOD: Two community panels were conducted in Melbourne with members of the Vietnamese (n = 11), Sudanes…

  • The introduction and demise of full-body computed tomography (CT) scanning in Australia: Implications for preventing overdiagnosis

    Open Access•Chris Degeling, Eliza J McEwin et al.•ARTICLE•Critical Public Health•2020

    Full-body computed tomography (CT) screening came to Australia in 2002. Within a year, public access to self-referred full-body CT screening was withdrawn as a consequence of sustained professional and political pressure and legislative changes. We examine how self-referred full-body CT scans were made available to Australian consumers, and evaluate the social, cultural and system factors that contributed to their de-implementation. Using histori…

  • Parenting and the vaccine refusal process: A new explanation of the relationship between lifestyle and vaccination trajectories

    Open Access•Kerrie E Wiley, Kerrie Wiley et al.•ARTICLE•Social Science & Medicine•2020•Cited by: 10•References: 18

  • Developing and applying a deductive coding framework to assess the goals of Citizen/Community Jury deliberations

    Open Access•Anna Mae Scott, Rebecca Sims et al.•ARTICLE•Health Expectations•2019

    BACKGROUND: Public participation in health policy decision making is thought to improve the quality of the decisions and enhance their legitimacy. Citizen/Community Juries (CJs) are a form of public participation that aims to elicit an informed community perspective on controversial topics. Reporting standards for CJ processes have already been proposed. However, less clarity exists about the standards for what constitutes a good quality CJ delib…

Next
  • Parenting and the vaccine refusal process: A new explanation of the relationship between lifestyle and vaccination trajectories

    Open Access•Kerrie E Wiley, Kerrie Wiley et al.•ARTICLE•Social Science & Medicine•2020•Cited by: 10•References: 18

  • Evidence, Ethics, and Values: A Framework for Health Promotion

    Stacy M Carter, Lucie Rychetnik et al.•ARTICLE•American Journal of Public Health•2011•Cited by: 10•References: 65

    We propose a new approach to guide health promotion practice. Health promotion should draw on 2 related systems of reasoning: an evidential system and an ethical system. Further, there are concepts, values, and procedures inherent in both health promotion evidence and ethics, and these should be made explicit. We illustrate our approach with the exemplar of intervention in weight, and use a specific mass-media campaign to show the real-world dang…

  • Influencing health policy through public deliberation: Lessons learned from two decades of Citizens'/community juries

    Open Access•Chris Degeling, Lucie Rychetnik et al.•ARTICLE•Social Science & Medicine•2017•Cited by: 9•References: 23

  • Getting evidence into policy: The need for deliberative strategies

    Open Access•Kathy Flitcroft, James Gillespie et al.•ARTICLE•Social Science & Medicine•2011•Cited by: 9•References: 15

  • Labels matter: Use and non-use of 'anti-vax' framing in Australian media discourse 2008-2018

    Open Access•Jay Court, Stacy M Carter et al.•ARTICLE•Social Science & Medicine•2021•Cited by: 8•References: 28

  • You Have to Make Something of All That Rubbish, Do You? An Empirical Investigation of the Social Process of Qualitative Research

    Open Access•Stacy M Carter, Christopher F C Jordens et al.•ARTICLE•Qualitative Health Research•2008•Cited by: 8•References: 24

    In this article, we examine participants' talk about qualitative research. We provide empirical support for post-structural theorizations of the interview and propose three distinct but related dimensions of qualitative research: emotional, purposive/relational, and epistemic/ontological. In this study, participants often became upset but constructed participation as enjoyable and cathartic. The purpose of participation was to assist the communit…

  • Balance, Balancing, and Health

    Open Access•Wendy L Lipworth, Wendy Lipworth et al.•ARTICLE•Qualitative Health Research•2011•Cited by: 7•References: 48

    In this article we explore the concept of balance in the context of health. We became interested in balance during a grounded theory study of lay conceptualizations of cancer risk in which participants were concerned with having a good life, which relied heavily on balancing processes. This led us to the qualitative literature about balance in the context of health, which was large and in need of synthesis. We identified 170 relevant studies and …

  • Writing social determinants into and out of cancer control: An assessment of policy practice

    Open Access•Stacy M Carter, Claire Hooker et al.•ARTICLE•Social Science & Medicine•2009•Cited by: 7•References: 8

  • Journal peer review in context: A qualitative study of the social and subjective dimensions of manuscript review in biomedical publishing

    Open Access•Wendy L Lipworth, Wendy Lipworth et al.•ARTICLE•Social Science & Medicine•2011•Cited by: 4•References: 3

  • Pragmatic pluralism: Mutual tolerance of contested understandings between orthodox and alternative practitioners in autologous stem cell transplantation

    Open Access•Miles Little, Christopher F C Jordens et al.•ARTICLE•Social Science & Medicine•2007•Cited by: 3•References: 29

  • Direct-to-consumer detection of atrial fibrillation in a smartwatch electrocardiogram: Medical overuse, medicalisation and the experience of consumers

    Open Access•Patti Shih, Kathleen Prokopovich et al.•ARTICLE•Social Science & Medicine•2022•Cited by: 2•References: 31

  • Decision-Making Preferences and Deprescribing: Perspectives of Older Adults and Companions About Their Medicines

    Open Access•Kristie Rebecca Weir, Kristie Weir et al.•ARTICLE•The Journals of Gerontology…•2017•Cited by: 2•References: 3

    This study provides a novel typology to describe differences between older people who are happy to take multiple medicines, and those who are open to deprescribing. To enable shared decision-making, prescribers need to adapt their communication about polypharmacy based on their patients' attitudes to medicines and preferences for involvement in decisions

  • Sharing precision medicine data with private industry: Outcomes of a citizens' jury in Singapore

    Open Access•Angela Ballantyne, Tamra Lysaght et al.•ARTICLE•Big Data & Society•2022•Cited by: 1•References: 33

    Precision medicine is an emerging approach to treatment and disease prevention that relies on linkages between very large datasets of health information that is shared amongst researchers and health professionals. While studies suggest broad support for sharing precision medicine data with researchers at publicly funded institutions, there is reluctance to share health information with private industry for research and development. As the private…

  • Smoking to fit a stigmatised identity? A qualitative study of marginalised young people in Australia

    Open Access•Marita Hefler, Stacy M Carter•ARTICLE•Health An Interdisciplinary…•2019•Cited by: 1•References: 46

    In countries with comprehensive tobacco control, smoking is increasingly denormalised, with smokers subject to social stigmatisation. Qualitative research and commentary about denormalisation and stigma has largely focused on the impact on current or former smokers. Little attention has been given to the interaction between existing stigma among socially marginalised and disadvantaged young people and its role in smoking uptake, maintenance and r…

  • Accounts from developers of generic health state utility instruments explain why they produce different Qalys: A qualitative study

    Open Access•Kristen Pickles, Emily Lancsar et al.•ARTICLE•Social Science & Medicine•2019•Cited by: 1•References: 25

  • Worshipping at the Alpine altar: Promoting tobacco in a world without advertising: Figure 1

    Stacy M Carter, Stacy Carter•ARTICLE•Tobacco Control•2001

    Glisten. The party to go with your glamourpuss dress." "Glisten. Music to go with your rock star hair." "Glisten. Cocktails to go with your spanking ring." ("Minimum age 18. Photo ID required. Tobacco & alcohol products for sale.") Three highly stylised advertisements, one for each by-line, and each featuring a young woman on the dancefloor flaunting dress, hair and ring respectively, had been splashed in expensive full colour across the street m…

  • Mongoven, Biscoe & Duchin: Destroying tobacco control activism from the inside

    Stacy M Carter•ARTICLE•Tobacco Control•2002

    Mongoven, Biscoe & Duchin, a specialist firm based in Washington DC, has honed a niche as expert intelligence gatherers, helping tobacco companies such as Philip Morris and RJ Reynolds to damage tobacco control efforts, including the WHO's Framework Convention on Tobacco Control

  • Preserved Olfactory Cuing of Autobiographical Memories in Old Age

    Elizabeth A Maylor, Stacy M Carter et al.•ARTICLE•The Journals of Gerontology…•2002•References: 1

    The authors investigated whether olfactory cues can facilitate memory retrieval and whether they retain their effectiveness in old age. In Phase 1, 57 young and 57 old adults (mean ages of 21 and 84 years, respectively) were asked to recall autobiographical memories associated with each of six cue words. In Phase 2, the same words were presented again with instructions to recall new memories; on this second occasion, half of the words were accomp…

  • Australia is one of the darkest markets in the world: The global importance of Australian tobacco control: Figure 1

    Simon Chapman, Fiona Byrne et al.•ARTICLE•Tobacco Control•2003

    Australia is one of the darkest markets in the world... it probably is the darkest, I mean ourselves and Canada fight every month for who's got the darkest conditions to do tobacco manufacturing and marketing. And one of the things we can offer the world is what we do best, which is how to work, maximize, proactively drive our market position in a market that's completely dark. Now that takes a different skillset... a different type of learning. …

  • Smokers and non-smokers talk about regulatory options in tobacco control

    Stacy M Carter, Simon Chapman•ARTICLE•Tobacco Control•2006

    Simple measures of agreement used in polls may obscure the complexity of community responses to tobacco policy. Support was frequently present but contested; some arguments that seem self-evident to advocates were not so to participants. The detailed understanding of laypeople's responses provided through qualitative methods may help frame proposals and arguments to meet concerns about justice, effectiveness and feasibility

  • Justifying Knowledge, Justifying Method, Taking Action: Epistemologies, Methodologies, and Methods in Qualitative Research

    Open Access•Stacy M Carter, Miles Little•ARTICLE•Qualitative Health Research•2007

    In this article, the authors clarify a framework for qualitative research, in particular for evaluating its quality, founded on epistemology, methodology, and method. They define these elements and discuss their respective contributions and interrelationships. Epistemology determines and is made visible through method, particularly in the participant— researcher relationship, measures of research quality, and form, voice, and representation in an…

  • Pragmatic pluralism: Mutual tolerance of contested understandings between orthodox and alternative practitioners in autologous stem cell transplantation

    Open Access•Miles Little, Christopher F C Jordens et al.•ARTICLE•Social Science & Medicine•2007•Cited by: 3•References: 29

  • You Have to Make Something of All That Rubbish, Do You? An Empirical Investigation of the Social Process of Qualitative Research

    Open Access•Stacy M Carter, Christopher F C Jordens et al.•ARTICLE•Qualitative Health Research•2008•Cited by: 8•References: 24

    In this article, we examine participants' talk about qualitative research. We provide empirical support for post-structural theorizations of the interview and propose three distinct but related dimensions of qualitative research: emotional, purposive/relational, and epistemic/ontological. In this study, participants often became upset but constructed participation as enjoyable and cathartic. The purpose of participation was to assist the communit…

  • Writing the risk of cancer: Cancer risk in public policy

    Claire Hooker, Stacy M Carter et al.•ARTICLE•Health Risk & Society•2009

    In this paper we examine how cancer risk is written in cancer policy documents from the English speaking OECD nations. We offer an audit of the multiple ways in which cancer risk is conceptualised and presented in health policy and professional contexts with the long term aim of comparing this with lay conceptualisations. Our study sampled cancer policy documents produced by six nations, the World Health Organization and the International Union f…

  • Writing social determinants into and out of cancer control: An assessment of policy practice

    Open Access•Stacy M Carter, Claire Hooker et al.•ARTICLE•Social Science & Medicine•2009•Cited by: 7•References: 8

  • Supporting Patient Autonomy: The Importance of Clinician-patient Relationships

    Open Access•Vikki Entwistle, Vikki A Entwistle et al.•ARTICLE•Journal of General Internal…•2010

  • Beliefs and beyond: What can we learn from qualitative studies of lay people’s understandings of cancer risk

    Open Access•Wendy L Lipworth, Wendy Lipworth et al.•ARTICLE•Health Expectations•2010

    Background Clinicians and public health professionals are centrally concerned with mediating risk. However, people often resist the risk‐related information that is communicated to them by experts, or have their own models of risk that conflict with expert views. Quantitative studies have clearly demonstrated the importance of health beliefs and various cognitive and emotional processes in shaping risk perception. More recently, a growing body of…

  • How to do a grounded theory study: A worked example of a study of dental practices

    Open Access•Alexandra Sbaraini, Stacy M Carter et al.•ARTICLE•BMC Medical Research Methodology•2011

    BACKGROUND: Qualitative methodologies are increasingly popular in medical research. Grounded theory is the methodology most-often cited by authors of qualitative studies in medicine, but it has been suggested that many 'grounded theory' studies are not concordant with the methodology. In this paper we provide a worked example of a grounded theory project. Our aim is to provide a model for practice, to connect medical researchers with a useful met…

  • When good evidence is not enough: The role of context in bowel cancer screening policy in New Zealand

    Kathy Flitcroft, James Gillespie et al.•ARTICLE•Evidence & Policy•2011•References: 2

    Bowel cancer is a serious health problem in developed countries. Australia, the United Kingdom (UK) and New Zealand (NZ) reviewed the same randomised controlled trial evidence on the benefits and harms of population-based bowel cancer screening. Yet only NZ, with the highest age standardised rate of bowel cancer mortality, decided against introducing a bowel cancer screening programme. This case study of policy making explores the unique resource…

  • Journal peer review in context: A qualitative study of the social and subjective dimensions of manuscript review in biomedical publishing

    Open Access•Wendy L Lipworth, Wendy Lipworth et al.•ARTICLE•Social Science & Medicine•2011•Cited by: 4•References: 3

  • Evidence, Ethics, and Values: A Framework for Health Promotion

    Stacy M Carter, Lucie Rychetnik et al.•ARTICLE•American Journal of Public Health•2011•Cited by: 10•References: 65

    We propose a new approach to guide health promotion practice. Health promotion should draw on 2 related systems of reasoning: an evidential system and an ethical system. Further, there are concepts, values, and procedures inherent in both health promotion evidence and ethics, and these should be made explicit. We illustrate our approach with the exemplar of intervention in weight, and use a specific mass-media campaign to show the real-world dang…

  • Getting evidence into policy: The need for deliberative strategies

    Open Access•Kathy Flitcroft, James Gillespie et al.•ARTICLE•Social Science & Medicine•2011•Cited by: 9•References: 15

  • Balance, Balancing, and Health

    Open Access•Wendy L Lipworth, Wendy Lipworth et al.•ARTICLE•Qualitative Health Research•2011•Cited by: 7•References: 48

    In this article we explore the concept of balance in the context of health. We became interested in balance during a grounded theory study of lay conceptualizations of cancer risk in which participants were concerned with having a good life, which relied heavily on balancing processes. This led us to the qualitative literature about balance in the context of health, which was large and in need of synthesis. We identified 170 relevant studies and …

  • Decision Making in a Crowded Room: The Relational Significance of Social Roles in Decisions to Proceed With Allogeneic Stem Cell Transplantation

    Open Access•Rowena Forsyth, Camilla Scanlan et al.•ARTICLE•Qualitative Health Research•2011•References: 41

    Researchers studying health care decision making generally focus on the interaction that unfolds between patients and health professionals. Using the example of allogeneic bone marrow transplant, in this article we identify decision making to be a relational process concurrently underpinned by patients' engagement with health professionals, their families, and broader social networks. We argue that the person undergoing a transplant simultaneousl…

  • Incorporating evidence and politics in health policy: Can institutionalising evidence review make a difference

    Kathy Flitcroft, James Gillespie et al.•ARTICLE•Evidence & Policy•2014

    Much of the evidence translation literature focuses narrowly on the use of evidence in the initial policy formulation stages, and downplays the crucial role of institutions and the inherently political nature of policy making. More recent approaches acknowledge the importance of institutional and political factors, but make no attempt to incorporate their influence into new models of evidence translation. To address this issue, this article uses …

  • Integrating relationship- and research-based approaches in Australian health promotion practice

    Open Access•Christiane Klinner, Stacy M Carter et al.•ARTICLE•Health Promotion International•2015

    We examine the perspectives of health promotion practitioners on their approaches to determining health promotion practice, in particular on the role of research and relationships in this process. Using Grounded Theory methods, we analysed 58 semi-structured interviews with 54 health promotion practitioners in New South Wales, Australia. Practitioners differentiated between relationship-based and research-based approaches as two sources of knowle…

  • Which public and why deliberate? – A scoping review of public deliberation in public health and health policy research

    Open Access•Chris Degeling, Stacy M Carter et al.•ARTICLE•Social Science & Medicine•2015

  • Literature Review of Multicultural Instrumentation

    Huda Sarraj, Stacy M Carter et al.•ARTICLE•Multicultural Perspectives•2015•References: 3

    Demographic changes at the national level emphasize a critical need for multicultural education to be included as part of undergraduate education. This critical review of the literature examines 10 multicultural instruments that are suitable for use in K–12 or higher education institutions. This is a novel literature review in that it is the first such review to investigate the contribution of each instrument to five multicultural components in e…

  • All care, but whose responsibility? Community juries reason about expert and patient responsibilities in prostate-specific antigen screening for prostate cancer

    Open Access•Chris Degeling, Stacy M Carter et al.•ARTICLE•Health An Interdisciplinary…•2016•References: 44

    General practitioners have implicitly been given responsibility for guiding men's decisions about prostate-specific antigen-based screening for prostate cancer, but patients' expectations of the bounds of this responsibility remain unclear. We sought to explore how well-informed members of the public allocate responsibilities in prostate-specific antigen screening decision-making. In 2014, we convened two Community juries in Sydney, Australia, to…

  • CJC heck Stage 1: Development and testing of a checklist for reporting community juries – Delphi process and analysis of studies published in 1996–2015

    Open Access•Rae Thomas, Rebecca Sims et al.•ARTICLE•Health Expectations•2017

    BACKGROUND: Opportunities for community members to actively participate in policy development are increasing. Community/citizen's juries (CJs) are a deliberative democratic process aimed to illicit informed community perspectives on difficult topics. But how comprehensive these processes are reported in peer-reviewed literature is unknown. Adequate reporting of methodology enables others to judge process quality, compare outcomes, facilitate crit…

Political science (41 works) · Medicine (39 works) · Psychology (38 works) · Sociology (26 works) · Public relations (20 works) · Computer Science (18 works) · Law (18 works) · Public health (16 works) · Nursing (15 works) · Social Psychology (15 works)

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