Breast cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients diagnosed with cStage 0~II breast cancer (histologically diagnosed as breast cancer and clinically diagnosed with stage 0~II) Patients who undergo surgery first Patients undergoing surgery at our hospital Patients who have received a sufficient explanation for participating in this study and who are able to obtain written consent from the patient to participate in the study with sufficient understanding and voluntary consent Patients over 18 years of age at the time of obtaining consent
Exclusion criteria
Exclusion criteria: Patients who are unable to use a tablet Patients undergoing preoperative chemotherapy Patients judged to be unsuitable as research subjects by the principal investigator or co-investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improvement of the SDM score (assessed by SDM-Q-9) | — |
Secondary
| Measure | Time frame |
|---|---|
| SDM-Q-Doc Decision Regret Scale Outpatient consultation hours Outpatient nurse interview hours Number of inquiries outside of the reservation Patient satisfaction assessment after using a tablet device Assessment of the patient's understanding by doctors | — |
Contacts
Okayama University Hospital