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Childhood cancer survivorship care: A qualitative study of healthcare providers’ professional preferences

Frontiers in oncology, 2022-10, Vol.12, p.945911-945911

2022

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Pilot testing “Teach Ted”: A digital application for children undergoing blood tests and their parents

PEC innovation, 2024-12, Vol.4, p.100251-100251, Article 100251

2024

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When to break the news and whose responsibility is it? A cross-sectional qualitative study of health professionals’ views regarding disclosure of BRCA genetic cancer risk

BMJ open, 2020-02, Vol.10 (2), p.e033127-e033127

2020

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The feasibility and acceptability of collecting psychosocial outcome measures embedded within a precision medicine trial for childhood cancer

Cancer medicine (Malden, MA), 2024-06, Vol.13 (12), p.e7339-n/a

2024

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Adapting the Voicing My CHOiCES Advance Care Planning Communication Guide for Australian Adolescents and Young Adults with Cancer: Appropriateness, Acceptability, and Considerations for Clinical Practice

Cancers, 2023-04, Vol.15 (7), p.2129

2023

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Online group-based cognitive-behavioural therapy for adolescents and young adults after cancer treatment: a multicenter randomised controlled trial of Recapture Life-AYA

BMC cancer, 2012-08, Vol.12 (1), p.339-339, Article 339

2012

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“We needed this”: perspectives of parents and healthcare professionals involved in a pilot newborn screening program for spinal muscular atrophy

EClinicalMedicine, 2021-03, Vol.33, p.100742-100742, Article 100742

2021

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Access to and experience of education for children and adolescents with cancer: a scoping review protocol

Systematic reviews, 2021-06, Vol.10 (1), p.1-167, Article 167

2021

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Quality of Life (QoL) of Children and Adolescents Participating in a Precision Medicine Trial for High-Risk Childhood Cancer

Cancers, 2022-10, Vol.14 (21), p.5310

2022

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The Perceived Impact of COVID-19 on the Mental Health Status of Adolescent and Young Adult Survivors of Childhood Cancer and the Development of a Knowledge Translation Tool to Support Their Information Needs

Frontiers in psychology, 2022-05, Vol.13, p.867151-867151

2022

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Psychological Outcomes, Health-Related Quality of Life, and Neurocognitive Functioning in Survivors of Childhood Cancer and Their Parents

The Pediatric clinics of North America, 2020-12, Vol.67 (6), p.1103-1134

2020

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Providing Psychological Support to Parents of Childhood Cancer Survivors: ‘Cascade’ Intervention Trial Results and Lessons for the Future

Cancers, 2021-11, Vol.13 (22), p.5597

2021

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Co-design of a paediatric oncology medicines database (ProCure) to support complex care provision for children with a hard-to-treat cancer

Frontiers in medicine, 2024-03, Vol.11, p.1332434-1332434

2024

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The Impact of the Early COVID-19 Global Pandemic on Children Undergoing Active Cancer Treatment and Their Parents

Current oncology (Toronto), 2023-02, Vol.30 (2), p.2441-2456

2023

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Gastroenterology services for patients with Cystic Fibrosis across Australia and New Zealand: a multi-stakeholder assessment of patients' and professionals' perspectives

Frontiers in pediatrics, 2023-12, Vol.11, p.1322941-1322941

2023

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Quitting intentions and behaviours among young Australian e‐cigarette users

Addiction (Abingdon, England), 2024-09, Vol.119 (9), p.1608-1615

2024

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Patient-reported depression measures in cancer: a meta-review

The Lancet. Psychiatry, 2015-07, Vol.2 (7), p.635-647

2015

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Hearing parents' voices: A priority-setting workshop to inform a suite of psychological resources for parents of children with rare genetic epilepsies

PEC innovation, 2022-12, Vol.1, p.100014-100014, Article 100014

2022

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Patterns and Predictors of Healthcare Use among Adolescent and Young Adult Cancer Survivors versus a Community Comparison Group

Cancers, 2021-10, Vol.13 (21), p.5270

2021

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Guidelines for Caring for the Social Well-Being of Adolescents and Young Adults with Cancer in Australia

Journal of adolescent and young adult oncology, 2024-02, Vol.13 (1), p.8-29

2024

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A Digital Educational Intervention With Wearable Activity Trackers to Support Health Behaviors Among Childhood Cancer Survivors: Pilot Feasibility and Acceptability Study

JMIR cancer, 2022-08, Vol.8 (3), p.e38367

2022

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Primary Care Physicians’ Perspectives of Their Role in Cancer Care: A Systematic Review

Journal of general internal medicine : JGIM, 2016-10, Vol.31 (10), p.1222-1236

2016

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Aligning intuition and theory: enhancing the replicability of behaviour change interventions in cancer genetics

Implementation science communications, 2020-10, Vol.1 (1), p.90-90, Article 90

2020

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Cancer Survivorship in the Indo-Pacific: Priorities for Progress

JCO global oncology, 2023-01, Vol.9 (9), p.e2200305-e2200305

2023

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Childhood cancer survivorship care: A qualitative study of healthcare providers’ professional preferences

Pilot testing “Teach Ted”: A digital application for children undergoing blood tests and their parents

Online, Group-Based Psychological Support for Adolescent and Young Adult Cancer Survivors: Results from the Recapture Life Randomized Trial

When to break the news and whose responsibility is it? A cross-sectional qualitative study of health professionals’ views regarding disclosure of BRCA genetic cancer risk

The feasibility and acceptability of collecting psychosocial outcome measures embedded within a precision medicine trial for childhood cancer

Adapting the Voicing My CHOiCES Advance Care Planning Communication Guide for Australian Adolescents and Young Adults with Cancer: Appropriateness, Acceptability, and Considerations for Clinical Practice

Online group-based cognitive-behavioural therapy for adolescents and young adults after cancer treatment: a multicenter randomised controlled trial of Recapture Life-AYA

“We needed this”: perspectives of parents and healthcare professionals involved in a pilot newborn screening program for spinal muscular atrophy

Access to and experience of education for children and adolescents with cancer: a scoping review protocol

Quality of Life (QoL) of Children and Adolescents Participating in a Precision Medicine Trial for High-Risk Childhood Cancer

The Perceived Impact of COVID-19 on the Mental Health Status of Adolescent and Young Adult Survivors of Childhood Cancer and the Development of a Knowledge Translation Tool to Support Their Information Needs

Psychological Outcomes, Health-Related Quality of Life, and Neurocognitive Functioning in Survivors of Childhood Cancer and Their Parents

Providing Psychological Support to Parents of Childhood Cancer Survivors: ‘Cascade’ Intervention Trial Results and Lessons for the Future

Co-design of a paediatric oncology medicines database (ProCure) to support complex care provision for children with a hard-to-treat cancer

The Impact of the Early COVID-19 Global Pandemic on Children Undergoing Active Cancer Treatment and Their Parents

Gastroenterology services for patients with Cystic Fibrosis across Australia and New Zealand: a multi-stakeholder assessment of patients' and professionals' perspectives

Quitting intentions and behaviours among young Australian e‐cigarette users

Patient-reported depression measures in cancer: a meta-review

Hearing parents' voices: A priority-setting workshop to inform a suite of psychological resources for parents of children with rare genetic epilepsies

Patterns and Predictors of Healthcare Use among Adolescent and Young Adult Cancer Survivors versus a Community Comparison Group

Guidelines for Caring for the Social Well-Being of Adolescents and Young Adults with Cancer in Australia

A Digital Educational Intervention With Wearable Activity Trackers to Support Health Behaviors Among Childhood Cancer Survivors: Pilot Feasibility and Acceptability Study

Primary Care Physicians’ Perspectives of Their Role in Cancer Care: A Systematic Review

Aligning intuition and theory: enhancing the replicability of behaviour change interventions in cancer genetics

Cancer Survivorship in the Indo-Pacific: Priorities for Progress

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