Table 1 Schedule of enrolment, variables and measures
Timepoint | Trial period | ||
|---|---|---|---|
Enrollment | Allocation | Post-allocation | |
Baseline | 0 | Post (7–10 days after randomization) | |
Registration and signed informed consent | X | ||
Allocation | X | ||
Demographics | X | ||
Use of internet | X | ||
Experience with other screenings | X | ||
Previous mammography | X | ||
Previous participation in screening programmes | X | ||
Family history of breast cancer | X | ||
Perceived risk of breast cancer | X | ||
Knowledge of breast cancer screening | X | X | |
Attitude to breast cancer screening | X | X | |
Intention regarding breast cancer screening | X | X | |
Satisfaction and acceptability of the information received | X | ||
Decisional conflict | X | ||