Web-based aftercare for oncological patients after inpatient rehabilitation: indication-specific development, process and outcome evaluation of the Onko-Vital eHealth aftercare module.
Not Applicable
- Conditions
- C50C51-C58C81-C96Malignant neoplasm of breastMalignant neoplasms of female genital organsMalignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue
- Registration Number
- DRKS00021525
- Lead Sponsor
- Verein zur Förderung der Rehabilitationsforschung e.V. Norderney c/o Deutsche Rentenversicherung, Westfalen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 334
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
Insufficient German language skills
Written Informed consent to the study is not available
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Measuring time: begin and end of rehabilitation, 3 and 6 months after discharge<br>Health-related quality of life (EORTC-QLQ-C30)
- Secondary Outcome Measures
Name Time Method Measuring time: begin and end of rehabilitation, 3 and 6 months after discharge<br>Participation (Index zur Messung von Einschränkungen der Teilhabe (IMET)<br>Distress Thermometer (DT)<br>Multidimensional Fatigue Inventary (MFI)<br>Hospital Anxiety and Depression Scale (HADS-scale)<br>Subjective prognosis of gainful employment (SPE-scale)