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Return to work after a cancer diagnosis: a meta-review of reviews and a meta-synthesis of recent qualitative studies

Journal of cancer survivorship, 2020-04, Vol.14 (2), p.114-134

2020

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Avoiding the ‘survivorship abyss’: Qualitative insights from 15‐year prostate cancer survivors

Psycho-oncology (Chichester, England), 2021-10, Vol.30 (10), p.1745-1755

2021

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Colorectal cancer survivorship: A systematic review and thematic synthesis of qualitative research

European journal of cancer care, 2021-07, Vol.30 (4), p.e13421-n/a

2021

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Identifying and Addressing Barriers to Treatment Decision-making in Bipolar II Disorder: Clinicians' Perspective

Australian psychologist, 2018-02, Vol.53 (1), p.40-51

2018

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Disability, psychological distress and quality of life in relation to cancer diagnosis and cancer type: population-based Australian study of 22,505 cancer survivors and 244,000 people without cancer

BMC medicine, 2020-12, Vol.18 (1), p.372-372, Article 372

2020

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Measuring female breast cancer survivors’ concerns about late effects of treatment: initial development of the Concerns about Late Effects in Oncology Questionnaire (CLEO)

Supportive care in cancer, 2022-04, Vol.30 (4), p.3563-3572

2022

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Work: saviour or struggle? A qualitative study examining employment and finances in colorectal cancer survivors living with advanced cancer

Supportive care in cancer, 2022-11, Vol.30 (11), p.9057-9069

2022

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Exploring the communication of oncologists, patients and family members in cancer consultations: development and application of a coding system capturing family-relevant behaviours (KINcode)

Psycho-oncology (Chichester, England), 2016-07, Vol.25 (7), p.787-794

2016

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The long haul: Lived experiences of survivors following different treatments for advanced colorectal cancer: A qualitative study

European journal of oncology nursing : the official journal of European Oncology Nursing Society, 2022-06, Vol.58, p.102123-102123, Article 102123

2022

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Pain and its interference with daily living in relation to cancer: a comparative population-based study of 16,053 cancer survivors and 106,345 people without cancer

BMC cancer, 2023-09, Vol.23 (1), p.1-11, Article 774

2023

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Evaluation of a novel individualised communication-skills training intervention to improve doctors’ confidence and skills in end-of-life communication

Palliative medicine, 2013-03, Vol.27 (3), p.236-243

2013

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Exploring the factors impacting choice and quality of overnight private hospital stays and consumer perspectives on patient reported experience measures (PREMs) in Australia: a qualitative interview study

Journal of patient-reported outcomes, 2024-07, Vol.8 (1), p.75-11, Article 75

2024

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Workforce participation in relation to cancer diagnosis, type and stage: Australian population-based study of 163,556 middle-aged people

Journal of cancer survivorship, 2022-04, Vol.16 (2), p.461-473

2022

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Fear of Cancer Progression and Death Anxiety in Survivors of Advanced Colorectal Cancer: A Qualitative Study Exploring Coping Strategies and Quality of Life

Omega: Journal of Death and Dying, 2022-09, p.302228221121493-302228221121493

2022

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Healthcare experiences of people with advanced colorectal cancer: A qualitative study

European journal of oncology nursing : the official journal of European Oncology Nursing Society, 2023-04, Vol.63, p.102265-102265, Article 102265

2023

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Supporting Carers: Study Protocol of a Meta-Review of Psychosocial Interventions for Carers of People With Cancer

JMIR research protocols, 2024-09, Vol.13, p.e56403

2024

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Development of Web-Based Education Modules to Improve Carer Engagement in Cancer Care: Design and User Experience Evaluation of the e-Triadic Oncology (eTRIO) Modules for Clinicians, Patients, and Carers

JMIR medical education, 2024-04, Vol.10, p.e50118-e50118

2024

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Intensive communication skills teaching for specialist training in palliative medicine: development and evaluation of an experiential workshop

Journal of palliative medicine, 2012-05, Vol.15 (5), p.585-591

2012

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Managing challenging interactions with family caregivers in the cancer setting: Guidelines for clinicians (TRIO Guidelines-2)

Patient education and counseling, 2018-06, Vol.101 (6), p.983-994

2018

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Family involvement in cancer treatment decision-making: A qualitative study of patient, family, and clinician attitudes and experiences

Patient education and counseling, 2016-07, Vol.99 (7), p.1146-1155

2016

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Facilitating collaborative and effective family involvement in the cancer setting: Guidelines for clinicians (TRIO Guidelines-1)

Patient education and counseling, 2018-06, Vol.101 (6), p.970-982

2018

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Recognising and managing the psychosocial needs of family carers: It’s time for change

Patient education and counseling, 2019-03, Vol.102 (3), p.401-403

2019

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The TRIO Framework: Conceptual insights into family caregiver involvement and influence throughout cancer treatment decision-making

Patient education and counseling, 2017-11, Vol.100 (11), p.2035-2046

2017

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Empowering family carers of people with multimorbidity as partners in chronic health care: Insights from health professionals

Patient education and counseling, 2022-12, Vol.105 (12), p.3550-3557

2022

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Patient readiness for shared decision making: A scoping review of qualitative literature

Patient education and counseling, 2023-04, Vol.109, p.9

2023

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Return to work after a cancer diagnosis: a meta-review of reviews and a meta-synthesis of recent qualitative studies

Avoiding the ‘survivorship abyss’: Qualitative insights from 15‐year prostate cancer survivors

Colorectal cancer survivorship: A systematic review and thematic synthesis of qualitative research

Identifying and Addressing Barriers to Treatment Decision-making in Bipolar II Disorder: Clinicians' Perspective

Disability, psychological distress and quality of life in relation to cancer diagnosis and cancer type: population-based Australian study of 22,505 cancer survivors and 244,000 people without cancer

Measuring female breast cancer survivors’ concerns about late effects of treatment: initial development of the Concerns about Late Effects in Oncology Questionnaire (CLEO)

Work: saviour or struggle? A qualitative study examining employment and finances in colorectal cancer survivors living with advanced cancer

Exploring the communication of oncologists, patients and family members in cancer consultations: development and application of a coding system capturing family-relevant behaviours (KINcode)

The long haul: Lived experiences of survivors following different treatments for advanced colorectal cancer: A qualitative study

Pain and its interference with daily living in relation to cancer: a comparative population-based study of 16,053 cancer survivors and 106,345 people without cancer

Evaluation of a novel individualised communication-skills training intervention to improve doctors’ confidence and skills in end-of-life communication

Exploring the factors impacting choice and quality of overnight private hospital stays and consumer perspectives on patient reported experience measures (PREMs) in Australia: a qualitative interview study

Workforce participation in relation to cancer diagnosis, type and stage: Australian population-based study of 163,556 middle-aged people

Fear of Cancer Progression and Death Anxiety in Survivors of Advanced Colorectal Cancer: A Qualitative Study Exploring Coping Strategies and Quality of Life

Healthcare experiences of people with advanced colorectal cancer: A qualitative study

Supporting Carers: Study Protocol of a Meta-Review of Psychosocial Interventions for Carers of People With Cancer

Development of Web-Based Education Modules to Improve Carer Engagement in Cancer Care: Design and User Experience Evaluation of the e-Triadic Oncology (eTRIO) Modules for Clinicians, Patients, and Carers

Intensive communication skills teaching for specialist training in palliative medicine: development and evaluation of an experiential workshop

Managing challenging interactions with family caregivers in the cancer setting: Guidelines for clinicians (TRIO Guidelines-2)

Family involvement in cancer treatment decision-making: A qualitative study of patient, family, and clinician attitudes and experiences

Facilitating collaborative and effective family involvement in the cancer setting: Guidelines for clinicians (TRIO Guidelines-1)

Recognising and managing the psychosocial needs of family carers: It’s time for change

The TRIO Framework: Conceptual insights into family caregiver involvement and influence throughout cancer treatment decision-making

Empowering family carers of people with multimorbidity as partners in chronic health care: Insights from health professionals

Patient readiness for shared decision making: A scoping review of qualitative literature

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