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An intervention was co-produced and outcome data secured for most trial participants, but the consent rate did not satisfy a 'stop/go' level of >=20% and a full trial is not feasible.
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Adam Noble
[Image - ORCID logo], Sarah Nevitt
[Image - ORCID logo], Emily Holmes
[Image - ORCID logo], Leone Ridsdale
[Image - ORCID logo], Myfanwy Morgan
[Image - ORCID logo], Catrin Tudur-Smith
[Image - ORCID logo], Dyfrig Hughes
[Image - ORCID logo], Steve Goodacre
[Image - ORCID logo], Tony Marson
[Image - ORCID logo] & Darlene Snape
[Image - ORCID logo].
Adam Noble 1,*, Sarah Nevitt 2, Emily Holmes 3, Leone Ridsdale 4, Myfanwy Morgan 5, Catrin Tudur-Smith 2, Dyfrig Hughes 3, Steve Goodacre 6, Tony Marson 7, Darlene Snape 1
1 Department of Health Services Research, University of Liverpool, Liverpool, UK
2 Department of Biostatistics, University of Liverpool, Liverpool, UK
3 Centre for Health Economics and Medicine Evaluation, Bangor University, Bangor, UK
4 Department of Basic and Clinical Neuroscience, King’s College London, London, UK
5 Institute of Pharmaceutical Science, King’s College London, London, UK
6 School of Health and Related Research, University of Sheffield, Sheffield, UK
7 Department of Molecular and Clinical Pharmacology, University of Liverpool, Liverpool, UK
* Corresponding author Email: adam.noble@liv.ac.uk
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