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A full trial is feasible with amendments to the recruitment process, outcome measure choice and intervention specification.
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Katherine Froggatt
[Image - ORCID logo], Ashley Best
[Image - ORCID logo], Frances Bunn
[Image - ORCID logo], Girvan Burnside
[Image - ORCID logo], Joanna Coast
[Image - ORCID logo], Lesley Dunleavy
[Image - ORCID logo], Claire Goodman
[Image - ORCID logo], Ben Hardwick
[Image - ORCID logo], Clare Jackson
[Image - ORCID logo], Julie Kinley
[Image - ORCID logo], Anne Davidson Lund, Jennifer Lynch
[Image - ORCID logo], Paul Mitchell
[Image - ORCID logo], Gareth Myring
[Image - ORCID logo], Shakil Patel
[Image - ORCID logo], Guillermo Perez Algorta
[Image - ORCID logo], Nancy Preston
[Image - ORCID logo], David Scott, Kate Silvera
[Image - ORCID logo] & Catherine Walshe
[Image - ORCID logo].
Katherine Froggatt 1, Ashley Best 2, Frances Bunn 3, Girvan Burnside 2, Joanna Coast 4, Lesley Dunleavy 1, Claire Goodman 3, Ben Hardwick 2, Clare Jackson 2, Julie Kinley 5, Anne Davidson Lund 6, Jennifer Lynch 3, Paul Mitchell 4, Gareth Myring 4, Shakil Patel 7, Guillermo Perez Algorta 1, Nancy Preston 1, David Scott 6, Kate Silvera 2, Catherine Walshe 1,*
1 International Observatory on End of Life Care, Faculty of Health and Medicine, Lancaster University, Lancaster, UK
2 Clinical Trials Research Centre, University of Liverpool, Liverpool, UK
3 Department of Health and Human Sciences, University of Hertfordshire, Hatfield, UK
4 Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK
5 Hospice UK, London, UK
6 Patient and public involvement member, UK, ,
7 Lancashire Clinical Trials Unit, University of Central Lancashire, Preston, UK
* Corresponding author Email: c.walshe@lancaster.ac.uk
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