• Use SMaRT with a prospective cohort, randomized controlled trial (RCT), cross-sectional, or qualitative study design

• Accommodate study staff and participants involved in multiple studies

• Specify study details, milestones for each arm or treatment group, site specific email addresses, automated notifications (email/text/push), and custom fields

• Create visit activities, task activities, or survey activities with custom URLs and survey completion feedback

• Insert ad hoc activities as needed on individual participant timelines

• Enter participants manually or import in bulk

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