C50 C71 D32 C61
Conditions
Interventions
Group 1: In the observational study, patient-reported endpoints (psychological, physical and social aspects) are recorded during standard therapy and correlated with traditional clinical target parame
Sponsors
Klinikum der Universität München, Campus Großhadern
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Indication for radiotherapy in the planned radiotherapy series at the Department of Radiotherapy, LMU University Hospital, Munich. Regarding Target Sample Size: The inclusion period is to be two years. No case number estimate is required, as the study is a prospective observational study.
Exclusion criteria
Exclusion criteria: Contraindications for radiotherapy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The objective of this study is to assess patient-related endpoints (psychological, physical and social aspects) during standard therapy and follow-up care. In addition, it will be investigated to what extent the results correlate between PRO (patient reported outcomes) and traditional clinical target values (e.g. acute toxicities, radiation dose to risk organs). | — |
Secondary
| Measure | Time frame |
|---|---|
| The query is made via the mobile eHealth application "CAREONLINE". Standardized patient- and/or tumor-entity-related questionnaires are provided for querying the experienced symptoms (presence, frequency, strength), abilities, behaviors or psychological sensitivities, which the patient can answer via the app. Standardized questionnaires (e.g. EORTC, FACT-B) are used for this purpose. The frequency of the query varies from daily to weekly, depending on the radiotherapy schedule. | — |
Countries
Germany
Contacts
Public ContactStefanie Corradini
Klinik und Poliklinik für Strahlentherapie undRadioonkologie
Outcome results
None listed