| Trial period | ||||||
---|---|---|---|---|---|---|---|
Enrolment | Allocation to intervention | Post-allocationa | |||||
Time point | 0 | 0 | 2–3 weeks | 1 month | 6 months | 12 months | 5 years |
Enrolment | |||||||
 Eligibility screen | X |  |  |  |  |  |  |
 Informed consent | X |  |  |  |  |  |  |
 Allocation to intervention |  | X |  |  |  |  |  |
Interventions | |||||||
 SCRIPT intervention |  |  | X (PRS report) |  |  |  |  |
 Control |  | X (cancer risk reduction brochure) |  |  |  | X (PRS report) |  |
Assessments | |||||||
 Demographics | X |  |  |  |  |  |  |
 CRC screening + health service utilisation data (GP record, MBS, NBCSP, VAED) |  |  |  |  |  | X | X |
 CRC screening data (participant report) | X |  |  | X | X | X |  |
 CRC risk perception | X |  |  | X | X | X |  |
 Cancer-specific anxiety (Cancer Worry Scale) | X |  |  | X | X | X |  |
 Influences of CRC screening behaviour (Preventative Health Model) | X |  |  | X | X | X |  |
 Cancer screening intentions | X |  |  | X | X | X |  |