C50 C51-C58 C81-C96
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Oncological rehabilitants (ICD-10: C50, D05; ICD-10: C51-C58; ICD-10: C81-C96) Use of mobile devices Written Informed consent to the study is available (informed consent)
Exclusion criteria
Exclusion criteria: Insufficient German language skills Written Informed consent to the study is not available
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measuring time: begin and end of rehabilitation, 3 and 6 months after discharge Health-related quality of life (EORTC-QLQ-C30) | — |
Secondary
| Measure | Time frame |
|---|---|
| Measuring time: begin and end of rehabilitation, 3 and 6 months after discharge Participation (Index zur Messung von Einschränkungen der Teilhabe (IMET) Distress Thermometer (DT) Multidimensional Fatigue Inventary (MFI) Hospital Anxiety and Depression Scale (HADS-scale) Subjective prognosis of gainful employment (SPE-scale) | — |
Countries
Germany
Contacts
Institut für Rehabilitationsforschung, NorderneyAbt. Bad Salzuflen