| Study period |  | ||||
---|---|---|---|---|---|---|
Enrolment | Allocation | Post-allocation | Close-out | |||
Timepoint | Pre-baseline | Baseline | Baseline | 6 months* | 12 months* | 18 months |
Enrolment | ||||||
 Eligibility screen | X |  |  |  |  |  |
 Informed consent | X |  |  |  |  |  |
 Allocation |  | X |  |  |  |  |
Interventions | ||||||
 GOSPEL 1 |  |  |  |  |  |  |
 Usual care |  |  |  |  |  |  |
Outcomes | ||||||
 Recruitment (feasibility) |  |  |  |  | X |  |
 Barriers and facilitators of care: optional interviews (feasibility) |  |  |  |  | X |  |
 Satisfaction of care |  |  |  |  | X |  |
 Medications history |  |  | X |  |  |  |
 HRQoL (FACT-Lym) |  |  | X | X | X |  |
 Patient experience of care |  |  | X | X | X |  |
 Symptom distress |  |  | X | X | X |  |
 Comorbidity burden |  |  | X |  | X |  |
 Dietary intake |  |  | X | X | X |  |
 Physical activity |  |  | X | X | X |  |
 Financial distress |  |  | X | X | X |  |
 Employment interference |  |  | X | X | X |  |
Participant characteristics | ||||||
 Demographics |  |  | X |  |  |  |
 Clinical characteristics |  |  | X |  |  |  |
Process Outcomes | ||||||
 Intervention fidelity: completion of checklists |  |  |  |  |  | X |
 Clinical encounters at cancer center |  |  |  |  |  | X |
 Cost analysis: resources to conduct the intervention |  |  |  |  |  | X |
 Safety indicators: clinical encounters, unscheduled clinic visits and rapid referrals back to acute care |  |  |  |  |  | X |