“…CRNs viewed themselves as patient advocates and referred to this role as their “ duty of care ” (Kyte et al, , p.6), throughout the patient's research journey and beyond (Kunhunny & Salmon, ; Larkin et al, ; Lawton et al, ; Loh, Butow, Brown, & Boyle, ; Schlichting, ; Tinkler et al, ). They considered patients first with the study taking second place (Höglund et al, ; Kyte et al, ; Larkin et al, ), and some were motivated to make the transition to the CRN role in pursuit of helping make a patient's life or health “ better ” (Rickard et al, , p.170). Even after the trial had finished, if contacted by patients, CRNs were happy to provide support (Schlichting, ).…”