C92.0 C82.2
Conditions
Interventions
Group 1: Longitudinal assessment of described patient-reported outcomes: T1-at beginning of cancer treatment, T2-interim staging according to the chemotherapy protocol, T3-last discharge after treatme
Sponsors
Universitätsklinik für Hämatologie und Onkologie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: ICD-10-C-diagnosis, ECOG < 3
Exclusion criteria
Exclusion criteria: palliative treatment, ECOG > 2
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| a. Validation of the Somatic Burden Score SBS-AE b. Aspects of mental health and somatopsychic symptoms in patients with haematological malignoms (e.g., general health perception, fatigue) assessed with the Medical Outcomes Study 36-Item Short Form Survey Instrument (SF-36), Patient Health Questionnaire (PHQ-D), Brief COPE and scale of general self-efficacy as longitudinal investigation: T1-at beginning of cancer treatment, T2-interim staging according to the chemotherapy protocol, T3-last discharge after treatment. | — |
Secondary
| Measure | Time frame |
|---|---|
| associations between the somatic burden of chemotherapy induced adverse events and mental distress outcomes of cancer patients. | — |
Countries
Germany
Contacts
Public ContactMichael Koehler
Universitätsklinik für Hämatologie und Onkologie
Outcome results
None listed