Malignancy
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Outpatients receiving pharmacotherapy for cancer Patients with a diagnosis of malignancy ECOG performance status 0-2 Age >=20 years at time of consent Prognosis expected to be at least 6 months as determined by physician Written informed consent Smartphone-enabled patients (or caregiver accessible)
Exclusion criteria
Exclusion criteria: Patients with obvious self-report difficulties due to their mental illness or cognitive impairment Concurrent participation in other PRO studies Patients with difficulty using a smartphone due to illness, adverse events, etc.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| EuroQol 5 dimensions 5-level(EQ-5D-5L) | — |
Secondary
| Measure | Time frame |
|---|---|
| Person-centred primary care measure (PCM) at the end of the study Number of patients followed up Number of tracing reports Number of Gan Yakubutsu Ryoho Taisei Jujitsu Kasan (Cancer chemotherapy system enhancement surcharge) Number of Renkei Jujitsu Kasan (coordination system enhancement surcharge) Consultation and Relational Empathy (CARE) measure at end of study Pharmacist's prescription suggestion Proportion of prescription suggestions made by pharmacists that were accepted by physicians Proportion of ePRO responses and alerts Number of Tokutei Yakuzai Kanri Shido Kasan 2 (specific medication management and consultation surcharge) Number of telephone follow-ups End of study questionnaire for healthcare professionals and patients | — |
Countries
Japan
Contacts
Saitama Medical University International Medical Center Department of Pharmacy