Table 2.

eRAPID RT study questionnaires and Case Report Forms (CRFs): participant completed

Questionnaire/CRF	Description of time points for completion	Baseline	3 weeks	6 weeks	9 weeks	12 weeks	18 weeks	24 weeks
Consent form	Baseline	X
Baseline: patient sociodemographic data form	Baseline	X
Baseline: computer usage questionnaire	Baseline	X
Patient-reported eRAPID symptom questionnaire (eRAPID intervention arm only)	Within 24 h of study entry and weekly during treatment and 6 weeks afterwards (12 weeks total). Then at 18 and 24 weeks.	X weekly	X weekly	X weekly	X weekly	X weekly	X (except rectal)	X (except rectal)
Patient Outcome Measures  FACT-G  EORTC-QLQ-C30  EQ-5D-5 L	Baseline, 6, 12 and 24 weeks	X		X		X		X
Self-efficacy, Lorig 6-item	Baseline and 12 weeks	X				X
Patient Activation Measure (PAM)	Baseline and 12 weeks	X				X
Use of resources form	6, 12 and 24 weeks			X		X		X
System Usability Scale	24 weeks (eRAPID intervention arm only)							X
Participant withdrawal feedback form	At point of withdrawal
End of study patient questionnaire	24 weeks							X
Clinician questionnaires
Clinician eRAPID feedback form (eRAPID intervention arm only)	At routine hospital appointments throughout the study		X	X	X	X	X (except rectal)	X (except rectal)
Clinician record of CTCAE	To be completed by clinician at the follow-up appointment 4–6 weeks after completion of treatment (exact time-point will be different for different disease groups)