Table 1.
MDMS for IDA | Study period – 3 months | |||
---|---|---|---|---|
Consent | Allocation | Post-allocation | Close-out | |
TIMEPOINT | 0 | 4 weeks | 3 months | |
ENROLMENT: | ||||
Eligibility screen | X | |||
Informed consent | X | |||
Allocation | X | |||
INTERVENTION: MDMS | ||||
ASSESSMENTS: | ||||
Primary outcome | ||||
Change in HbA1c | X | X | ||
Secondary outcomes | ||||
Serum fructosamine, patient satisfaction survey, | X | X | ||
Patient acceptability of MDMS survey | X | |||
Self-reported hypoglycaemic events survey | X | X | X | |
Healthcare provider (CDE) satisfaction survey | X | |||
Completion rate of IDA | X | |||
Clinician time, diabetes-related visits to CDE/GP/hospital |
CDE, credentialed diabetes educator; GP, general practitioner; HbA1c, glycated haemoglobin; IDA, insulin dose adjustment; MDMS, mobile diabetes management system.