C00-C97
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Diagnosis of a solid tumor; outpatient tumor treatment in the Oncological Outpatient Department of Internal Oncology of the Johanniter Hospital in Bonn; written consent of the patient; ability to speak and understand German
Exclusion criteria
Exclusion criteria: Diseases where the patient is unable to understand the type and content of the study and it can be excluded that the patient correctly understands the questionnaire or is able to fill it out on his own (e.g. Alzheimer's disease); intention to change the location of treatment in the near future
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of patients with at least one toxicity score 3-4 according to PRO-CTCAE referring to the symptoms nausea and vomiting, mucositis, fatigue, pain, diarrhea, constipation, dry mouth, dysphagia, loss of appetite, sleep disorders (at the beginning of every treatment cycle retrospectively assessed over the past seven days for a maximum of six treatment cycles) | — |
Secondary
| Measure | Time frame |
|---|---|
| Percentage of patients with toxicity, i.e. with score >0 according to PRO-CTCAE (at the beginning of every treatment cycle); quality of life for the patients using EORTC QLQ-C30 questionnaire and EQ-5D-3L questionnaire (at the beginning of every treatment cycle); patient satisfaction with the information on cancer treatment according to PS-CaTE (at the beginning of the first and last treatment cycle); frequency of occurrence of malnutrition (SGA category C) (at the beginning of every treatment cycle); percentage of patients with current, written medication plan (at the beginning of every treatment cycle) | — |
Countries
Germany
Contacts
Klinische Pharmazie