Table 1 Outcome measures and data collection timepoints for patients
Outcome measures | Timepoints | |
|---|---|---|
(T1) One week after the primary care consultation where CRC screening is discussed | (T2) 1 year after the CRC screening consultation | |
Number of eligible patients identified and successfully enrolled | X | |
Number of patients enrolled who receive the patient-facing intervention | X | |
Discontinuation rate | X | |
CRC screening uptake (primary outcome) with self-report item | X | |
Screening intention (1 items) | X | |
Knowledge of CRC screening (2 items) | X | X |
Patient activation (13 items) | X | X |
Health literacy (7 items) | X | |
EPICES (11 items) | X | |
SURE (4 items) | X | |
Was the questionnaire completed alone? (1 item) | X | X |
Demographics (9 items) | X | |
Total number of self-report items per timepoint | 48 | 17 |