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Australian experiences of out-of-pocket costs and financial burden following a cancer diagnosis: a systematic review

Psychometric properties of leadership scales for health professionals: a systematic review

System-wide and group-specific health service improvements: cross-sectional survey of outpatient improvement preferences and associations with demographic characteristics

Taking the pulse of the health services research community: A cross-sectional survey of research impact, barriers and support

Patients' experiences and preferences for opt-in models and health professional involvement in biobanking consent: a cross-sectional survey of Australian cancer outpatients

Facilitating High Quality Cancer Care: A Qualitative Study of Australian Chairpersons' Perspectives on Multidisciplinary Team Meetings

Enlisting the willing: a study of healthcare professional-initiated and opt-in biobanking consent reveals improvement opportunities throughout the registration process

Cross-sectional data that explore the relationship between outpatients' quality of life and preferences for quality improvement in oncology settings

Implementing systematic screening and structured care for distressed callers using Cancer Council's telephone services: protocol for a randomized stepped-wedge trial

A systematic review of barriers to optimal outpatient specialist services for individuals with prevalent chronic diseases: what are the unique and common barriers experienced by patients in high income countries?

Consumer participation in quality improvements for chronic disease care: development and evaluation of an interactive patient-centered survey to identify preferred service initiatives

Getting right to the point: identifying Australian outpatients' priorities and preferences for patient-centred quality improvement in chronic disease care

Collaborative patient-centered quality improvement: a cross-sectional survey comparing the types and numbers of quality initiatives selected by patients and health professionals

A cross-sectional audit of current practices and areas for improvement of distress screening and management in Australian cancer services: is there a will and a way to improve?

Consumer input into health care: Time for a new active and comprehensive model of consumer involvement

Not seeing the forest for the trees: a systematic review of comprehensive distress management programs and implementation strategies

A qualitative study investigating Australian cancer service outpatients’ experience of distress screening and management: what is the personal relevance, acceptability and improvement opportunities from patient perspectives?

Impact of financial costs of cancer on patients - the Australian experience

Protocol for a randomized controlled trial of proactive web-based versus telephone-based information and support: can electronic platforms deliver effective care for lung cancer patients?

Implementation of lung cancer multidisciplinary teams: a review of evidence-practice gaps

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