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Article History

Received: 30 July 2017

Accepted: 19 June 2018

First Online: 26 June 2018

Authors’ information

: Liz Gill, <i>Dip PT, BSc PT, MBA, MA and PhD</i>, is a Research Fellow. She has worked as a health professional in the areas of direct service provision; health system design; policy and consulting. Her research interests are in the areas of service co-creation in health services, and the role and contribution of the client to health service quality and service outcomes.Sandra Bradley, <i>RN, BSc, BArts, BN, Masters (Research) and PhD</i> is a Research Fellow conducting research in all areas of end of life care. With both qualitative and quantitative research skills her areas of interest focus on the decision-making that occurs by people assessing end of life care options.Ian Cameron<i>, MBBS PhD FAFRM (RACP),</i> is a Consultant Physician in Rehabilitation Medicine, Chair in Rehabilitation Medicine and Head of the Rehabilitation Studies Unit, Sydney Medical School, at the University of Sydney. Ian has a National Health and Medical Research Council Practitioner Fellowship and is a clinician researcher.Julie Ratcliffe, <i>BA Hons and PhD</i> is Professor in Health Economics at the Institute for Choice, University of South Australia. She has a strong track record in health economics research and teaching. Areas of research expertise include measurement & valuation of health outcomes, new/emerging healthcare technologies and healthcare preferences.

: This study was approved by the Flinders University Social and Behavioural Research Ethics Committee (Project Number 6448). Written consent to participate was obtained from all participants.

: Not applicable.

: Ian Cameron is a member of the editorial board.

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