breast cancer
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The patient is 20 years of age or older at the time consent is obtained Patients with access to a smartphone Patients who have given written consent to the study
Exclusion criteria
Exclusion criteria: Patients who are unable to use smartphones Patients with brain metastases and associated cognitive dysfunction Patients participating in another clinical study within 28 days prior to enrollment Patients with a performance status of 3 or higher
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| burden, satisfaction, and anxiety associated with app use by patients, pharmacy pharmacists, and physicians(The survey was conducted at two time points: before implementation and in the 6th month after implementation.) | — |
Secondary
| Measure | Time frame |
|---|---|
| adverse events, adherence, relative dose intensity (RDI),app input implementation rate, duration of treatment (days) and time to treatment failure (TTF), number of emergency consultations/admissions (times) associated with AEs, interview times at the outpatient pharmacist office (time to check the medication status and symptoms), number of times the pharmacist confirmed the patient's input (the number of times an alert message was confirmed), number of times free messages were added to the diary in the app (from patients to pharmacists and from pharmacists to patients), number of direct calls to the outpatient pharmacist office and the time (minutes) spent on that call. | — |
Countries
Japan
Contacts
Saitama Medical University Saitama International Medical Center pharmacy