Patient-reported outcomes in the treatment of oncological patients - A multicentred pilot study to select appropriate assessment instruments
- Conditions
- C00-D48Neoplasms
- Registration Number
- DRKS00005337
- Lead Sponsor
- Wilhelm-Roux-Förderprogramm der Medizinischen Fakultät der Martin-Luther-Universität Halle-Wittenberg, Prodekanat Forschung
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 71
Inclusion Criteria
Cancer patients, aged >18 Years, heterogenious diagnoses, undergoing in and/ or out-patient treatment who gave written informed consent.
Exclusion Criteria
non-sufficient understanding of the German language, cognitive impairments (e.g. dementia) or not able to give informed consent.
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method A modular assessment tool that fulfils the requirements of both patients and practitioners to facilitate supportive therapy and symptom management of oncologic patients.
- Secondary Outcome Measures
Name Time Method