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Anne Parkinson

Biographic Data

ID293126
NAMEAnne Parkinson
GIVEN NAMESAnne
FAMILY NAMEParkinson
SIGNATUREPARKINSON A
AFFILIATIONSGriffith University
ORCID0000-0001-9053-0707
VERIFIEDYes
TOTAL WORKS11
TOTAL CITATIONS8
AUTHOR COUNT11
EDITOR COUNT0
FIRST PUBLICATION YEAR1981
LATEST PUBLICATION YEAR2026
H-INDEX2
  • Consumer Engagement in Chronic Conditions Research

    Open Access•Mingming Zhou, Anne Parkinson et al.•ARTICLE•Health Expectations•2026

    BACKGROUND: Consumer engagement ensures that health research reflects lived experiences and generates outcomes relevant to those most affected. However, frameworks guiding engagement in research about chronic conditions remain limited and often lack theoretical grounding. OBJECTIVE: To develop an integrated, evidence-based framework to support consumer engagement in research about chronic conditions. METHODS: We integrated findings from (1) a sco…

  • Lived experience of out-of-pocket costs of health care and medicines by people with chronic conditions and their families in Australia

    Open Access•Jane Desborough, Charles Maskell-Knight et al.•ARTICLE•Health Policy•2025

  • A framework for involving coproduction partners in research about young people with type 1 diabetes

    Open Access•Jane Desborough, Anne Parkinson et al.•ARTICLE•Health Expectations•2022

    BACKGROUND: Involvement of end-users in research can enhance its quality, relevance, credibility and legitimacy; however, the processes through which these changes occur are unclear. Our aim was to explore a coproduction research team's experiences of their involvement in research about young people with type 1 diabetes mellitus (T1DM). METHODS: Semi-structured interviews conducted with two young people with T1DM, two parents, one diabetes educat…

  • Intertwined like a double helix

    Open Access•Anne Parkinson, Crystal Brunoro et al.•ARTICLE•Health Expectations•2022

  • ‘They're getting a taste of our world’

    Open Access•Anne Parkinson, Janet Drew et al.•ARTICLE•Health Expectations•2021

    BACKGROUND: People with multiple sclerosis (MS), who are often immunocompromised, require complex care and engage with a variety of health-care providers to manage their health. OBJECTIVE: To elucidate people with MS' experiences of accessing health care during the COVID-19 pandemic in Australia. DESIGN: A qualitative study involving semi-structured interviews and thematic analysis. SETTINGS AND PARTICIPANTS: Eight adults with a clinical diagnosi…

  • ‘It struck at the heart of who I thought I was’

    Open Access•Jane Desborough, Crystal Brunoro et al.•ARTICLE•Health Expectations•2020

  • Experiencing integration in Australian primary health care

    Open Access•Anne Parkinson, Melanie Banfield et al.•ARTICLE•International Journal of…•2016

    Introduction: Integrated care means different things to different people. We often find the terms ‘integration’ and ‘integrated care’ used interchangeably. However, Kodner and Spreeuwenberg (2002) suggest ‘integration’ refers to structures and processes, while ‘integrated care’ refers more to patient experiences and the outcomes of such processes. Contributing further to its complexity, integration occurs between different levels of the health sy…

  • Time to manage

    Open Access•T Jowsey, Denni et al.•ARTICLE•Sociology of Health & Illness•2016•Cited by: 6•References: 9

    This paper examines how people with chronic illnesses respond to absences of continuity and coordination of care. Little work has been done on how the ill person might mitigate flaws in a less than optimal system. Our qualitative research, carried out among 91 participants in Australia, reveals that people with chronic illnesses create strategies to facilitate the management of their care. These strategies included efforts to improve communicatio…

  • Does it matter who organises your health care

    Open Access•Paresh Dawda, Ian McRae et al.•ARTICLE•International Journal of…•2015

    In moving towards care coordination there are opportunities to improve the care coordination process itself, and the key enablers to improving care coordination appear to be the availability and communication of clinical information and the role of the clinical team

  • The public inquiry as a contested political technology

    Richard Hindmarsh, Anne Parkinson•ARTICLE•Environmental Politics•2012•Cited by: 2•References: 13

    In 2007, the Australian states of Victoria and New South Wales held reviews of their moratoriums on the commercial release of genetically modified (GM) food crops. The public inquiry form of review selected offered the best strategic pathway to amend these moratoriums to allow commercial release. As such, the reviews represented ‘political technologies’. This proposition is informed by: their formation within a policy context of pro-GM developmen…

  • Distributive industry in the UK to the year 1995

    Open Access•Anne Parkinson, A M Parkinson et al.•ARTICLE•Futures•1981

  • Time to manage

    Open Access•T Jowsey, Denni et al.•ARTICLE•Sociology of Health & Illness•2016•Cited by: 6•References: 9

    This paper examines how people with chronic illnesses respond to absences of continuity and coordination of care. Little work has been done on how the ill person might mitigate flaws in a less than optimal system. Our qualitative research, carried out among 91 participants in Australia, reveals that people with chronic illnesses create strategies to facilitate the management of their care. These strategies included efforts to improve communicatio…

  • The public inquiry as a contested political technology

    Richard Hindmarsh, Anne Parkinson•ARTICLE•Environmental Politics•2012•Cited by: 2•References: 13

    In 2007, the Australian states of Victoria and New South Wales held reviews of their moratoriums on the commercial release of genetically modified (GM) food crops. The public inquiry form of review selected offered the best strategic pathway to amend these moratoriums to allow commercial release. As such, the reviews represented ‘political technologies’. This proposition is informed by: their formation within a policy context of pro-GM developmen…

  • Distributive industry in the UK to the year 1995

    Open Access•Anne Parkinson, A M Parkinson et al.•ARTICLE•Futures•1981

  • The public inquiry as a contested political technology

    Richard Hindmarsh, Anne Parkinson•ARTICLE•Environmental Politics•2012•Cited by: 2•References: 13

    In 2007, the Australian states of Victoria and New South Wales held reviews of their moratoriums on the commercial release of genetically modified (GM) food crops. The public inquiry form of review selected offered the best strategic pathway to amend these moratoriums to allow commercial release. As such, the reviews represented ‘political technologies’. This proposition is informed by: their formation within a policy context of pro-GM developmen…

  • Does it matter who organises your health care

    Open Access•Paresh Dawda, Ian McRae et al.•ARTICLE•International Journal of…•2015

    In moving towards care coordination there are opportunities to improve the care coordination process itself, and the key enablers to improving care coordination appear to be the availability and communication of clinical information and the role of the clinical team

  • Experiencing integration in Australian primary health care

    Open Access•Anne Parkinson, Melanie Banfield et al.•ARTICLE•International Journal of…•2016

    Introduction: Integrated care means different things to different people. We often find the terms ‘integration’ and ‘integrated care’ used interchangeably. However, Kodner and Spreeuwenberg (2002) suggest ‘integration’ refers to structures and processes, while ‘integrated care’ refers more to patient experiences and the outcomes of such processes. Contributing further to its complexity, integration occurs between different levels of the health sy…

  • Time to manage

    Open Access•T Jowsey, Denni et al.•ARTICLE•Sociology of Health & Illness•2016•Cited by: 6•References: 9

    This paper examines how people with chronic illnesses respond to absences of continuity and coordination of care. Little work has been done on how the ill person might mitigate flaws in a less than optimal system. Our qualitative research, carried out among 91 participants in Australia, reveals that people with chronic illnesses create strategies to facilitate the management of their care. These strategies included efforts to improve communicatio…

  • ‘It struck at the heart of who I thought I was’

    Open Access•Jane Desborough, Crystal Brunoro et al.•ARTICLE•Health Expectations•2020

  • ‘They're getting a taste of our world’

    Open Access•Anne Parkinson, Janet Drew et al.•ARTICLE•Health Expectations•2021

    BACKGROUND: People with multiple sclerosis (MS), who are often immunocompromised, require complex care and engage with a variety of health-care providers to manage their health. OBJECTIVE: To elucidate people with MS' experiences of accessing health care during the COVID-19 pandemic in Australia. DESIGN: A qualitative study involving semi-structured interviews and thematic analysis. SETTINGS AND PARTICIPANTS: Eight adults with a clinical diagnosi…

  • A framework for involving coproduction partners in research about young people with type 1 diabetes

    Open Access•Jane Desborough, Anne Parkinson et al.•ARTICLE•Health Expectations•2022

    BACKGROUND: Involvement of end-users in research can enhance its quality, relevance, credibility and legitimacy; however, the processes through which these changes occur are unclear. Our aim was to explore a coproduction research team's experiences of their involvement in research about young people with type 1 diabetes mellitus (T1DM). METHODS: Semi-structured interviews conducted with two young people with T1DM, two parents, one diabetes educat…

  • Intertwined like a double helix

    Open Access•Anne Parkinson, Crystal Brunoro et al.•ARTICLE•Health Expectations•2022

  • Lived experience of out-of-pocket costs of health care and medicines by people with chronic conditions and their families in Australia

    Open Access•Jane Desborough, Charles Maskell-Knight et al.•ARTICLE•Health Policy•2025

  • Consumer Engagement in Chronic Conditions Research

    Open Access•Mingming Zhou, Anne Parkinson et al.•ARTICLE•Health Expectations•2026

    BACKGROUND: Consumer engagement ensures that health research reflects lived experiences and generates outcomes relevant to those most affected. However, frameworks guiding engagement in research about chronic conditions remain limited and often lack theoretical grounding. OBJECTIVE: To develop an integrated, evidence-based framework to support consumer engagement in research about chronic conditions. METHODS: We integrated findings from (1) a sco…

Psychology (6 works) · Medicine (5 works) · Qualitative research (5 works) · Sociology (5 works) · Health care (4 works) · Nursing (4 works) · Political science (4 works) · Family medicine (3 works) · Mental Health and Patient Involvement (3 works) · Multiple Sclerosis Research Studies (3 works)

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