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Timeline for study participants
| Schedule of events | |||
|---|---|---|---|
| Day 0 visit | Day 7 visit (+/− 2 days) | Unscheduled visit | |
| Informed consent and enrolment | x | ||
| Demographic data collection | x | ||
| History/physical examination | x | x | x |
| Diagnostic tests | x | ||
| Treatment prescription | x | x | |
| Patient adherence evaluation | x | x | |
| Collection of qualitative data | x | x | |
| Delivery of communication messages | x | ||
| Adverse event monitoring (see Safety reporting section) | x | x | |
