Feasibility and acceptability of an evidence-informed digital intervention to support self-management in people with non-alcoholic fatty liver disease: protocol for a non-randomised feasibility study (VITALISE)

Table 3 Feasibility study parameters

Parameter	Method of assessment
Recruitment rate	The number of eligible patients invited, who provide informed consent to participate in the study, versus those who decline, with reason(s) recorded
Intervention uptake, engagement and adherence	The number of patients who login to access VITALISE The mean and median number of times VITALISE is accessed over the 6-month time period
Completion and follow-up rate	The number of patients who complete the intervention, baseline and follow-up assessment outcome measures. Reasons for loss to follow-up will also be recorded

ISSN: 2055-5784