C00-C97
Conditions
Interventions
Group 1: Tumor patients at the Comprehensive Cancer Center Ulm with the use of integrative oncology measures.
Patient data will be collected with questionnaires for all fields during a Baseline visit
Sponsors
Universitätsklinik Ulm
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients diagnosed with cancer treated at the CCCU Written informed consent Ability to understand character and individual consequences of the clinical trial
Exclusion criteria
Exclusion criteria: Clinically significant concomitant disease critically influencing the ability of the patient to protocol adequate behavior Any finding that, in the judgment of the study investigator, renders the participant unsuitable for the study protocol
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Integrative oncology measures used | — |
Secondary
| Measure | Time frame |
|---|---|
| Demography, oncologic diagnosis and treatment as defined in the “onkologischer Basisdatensatz 2021” (oncology baseline data set 2021) Socieconomic data following the “Demographische Standards” of the German Federal Statistical Office Lifestyle data Quality of life (EORTC QLQ-C303) Fatigue (EORTC QLQ-FA124) Sleep (PSQI5) Depression and anxiety (PHQ-46) Symptoms from cancer and cancer treatment (PRO-CTCAE7) Patient satisfaction (EORTC PATSAT-C338) Symptom score (MYMOP29) | — |
Countries
Germany
Contacts
Public ContactPaul G. Werthmann
Universitätsklinik Ulm
Outcome results
None listed