Clinician consent | Pre-visit | Visit | Post-visit | ~3 months | |
---|---|---|---|---|---|
Baseline Clinician Survey | |||||
Demographics | ✓ | ||||
Professional practice | ✓ | ||||
Baseline Patient Survey | |||||
Quality of life | |||||
Overall | ✓ | ✓ | |||
Emotional well-being | ✓ | ✓ | |||
Physical well-being | ✓ | ✓ | |||
Intellectual well-being | ✓ | ✓ | |||
Social activity | ✓ | ✓ | |||
Spiritual well-being | ✓ | ✓ | |||
Pain | ✓ | ✓ | |||
Fatigue | ✓ | ✓ | |||
Support from friends/family | ✓ | ✓ | |||
Treatment burden on self | ✓ | ✓ | |||
Treatment burden on family | ✓ | ✓ | |||
Functional literacy | ✓ | ✓ | |||
Demographics | ✓ | ✓ | |||
Observation | |||||
RIAS coding | ✓ | ||||
Post-Encounter Patient Survey | |||||
Agenda setting in visit | ✓ | ||||
Patient-centeredness | ✓ | ||||
Concerns not discussed | ✓ | ||||
Shared decision-making | ✓ | ||||
Clinician rating | ✓ | ||||
Visit satisfaction | ✓ | ||||
Quality control- observation bias | ✓ | ||||
Post-Encounter Clinician Survey | |||||
Patient position on cancer control spectrum | ✓ | ||||
Decision made | ✓ | ||||
Quality of visit | ✓ | ||||
3-Month Follow up Patient Survey | |||||
Quality of life | ✓ | ✓ | |||
Overall | ✓ | ✓ | |||
Emotional well-being | ✓ | ✓ | |||
Physical well-being | ✓ | ✓ | |||
Intellectual well-being | ✓ | ✓ | |||
Social activity | ✓ | ✓ | |||
Spiritual well-being | ✓ | ✓ | |||
Pain | ✓ | ✓ | |||
Fatigue | ✓ | ✓ | |||
Support | ✓ | ✓ | |||
Treatment burden on self | ✓ | ✓ | |||
Treatment burden on family | ✓ | ✓ | |||
Cancer care decision-making preference and experience | ✓ | ||||
CAM use | ✓ | ||||
Chart Review | |||||
Location of patient care | ✓ | ||||
Insurance | ✓ | ||||
Family cancer history | ✓ | ||||
General cancer information | ✓ | ||||
Complementary and integrative medicine referrals | ✓ | ||||
Cancer related CAM use | ✓ | ||||
Post-Study Clinician Survey | |||||
Discussing CAM | ✓ | ||||
Discussing psychosocial issues | ✓ | ||||
Discussing End-of-life care | ✓ |