Lo scenario
A parallel-arm randomized trial evaluating a diabetes intervention, following CONSORT guidelines for transparent reporting of participant flow.
Cosa contiene questo disegno
Leggi le decisioni che ne stanno alla base.
01
Participants assessed for eligibility and reasons for exclusion recorded.
02
Random assignment to intervention or control.
03
Tracking of intervention receipt and follow-up losses.
04
Intention-to-treat analysis including all randomized participants.
When designing or reporting a clinical trial to ensure clear participant flow documentation as per CONSORT.