Advanced solid cancer
Conditions
Interventions
None listed
Sponsors
NTT Medical Center Tokyo.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients who; Be at least 20 years old Has been informed by a physician that he/she has cancer Be scheduled to receive new drug therapy in an outpatient chemotherapy unit at a medical facility in this country (regardless of treatment history) Can use smartphones Electronic written informed consent is submitted.
Exclusion criteria
Exclusion criteria: Oral intake is impossible. Planned long-term hospitalization, such as undergoing standby surgery or undergoing major surgery during the study period Any other information that the researcher deems inappropriate for this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Adverse events related to the meaningful caloric intake change | — |
Secondary
| Measure | Time frame |
|---|---|
| Weight and nutrition-related items by severity and duration of each adverse event. Describe nutrition-related items for the duration of adverse event occurrence relative to the duration of no adverse event occurrence. Describe the weight of the period of adverse event occurrence relative to the period of no adverse event occurrence. | — |
Countries
Japan
Contacts
Public ContactTakuro Mizukami
NTT Medical Center Tokyo Department of Medical Oncology
Outcome results
None listed