Breast cancer
Conditions
Interventions
Healthcare professionals, guiding patients facing the decision for follow-up care, will be introduced to a patient decision aid including (personalised) care outcomes, to support the process of shared
Sponsors
Santeon
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients must be facing the decision for the organisation of follow-up care after receiving curative treatment for invasive breast cancer (in the first follow-up consultation about 1 year after surgery); 2) Being treated in a Santeon hospital; 3) = 18 years of age; 4) Understand the Dutch language in speech and writing, and; 5) Able to provide informed consent.
Exclusion criteria
Exclusion criteria: 1) Patients diagnosed with non-invasive breast cancer (e.g. Ductal Carcinoma In Situ (DCIS)); 2) Patients who receive palliative treatment; 3) Patients who received neoadjuvant therapy; 4) Male breast cancer patients; 5) Patients with dementia; 6) Patients who received treatment for a recurrence or second primary tumor; 7) Patients with a breast cancer-related gene alteration (e.g. BRCA).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Patients' perceived level of involvement in the decision-making process (using the SDM-Q-9). | — |
Secondary
| Measure | Time frame |
|---|---|
| Patients' involvement in the decision-making process from the observers' viewpoint (using the OPTION-5). | — |
Contacts
Public ContactMariska Hackert
Santeon
Outcome results
None listed