Tablet-based computer-assisted data collection of functional aspects and quality of life by patients with head and neck tumors without and with direct feedback to the attending physician in a prospective controlled care study in the Department of Otorhinolaryngology, Head and Neck Surgery, University Clinic of Schleswig-Holstein Campus Lübeck
Not Applicable
- Conditions
- comorbidityquality of lifeburden of symptomsfunctional impairment adverse events according to the Common Terminology Criteria for Adverse Events (CTCAE v4)C01C02C03C04C05C06C07C08C09
- Registration Number
- DRKS00014230
- Lead Sponsor
- niversität zu Lübeck
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 319
Inclusion Criteria
Patients with diagnosis ICD-10 C01-C10, C12-13 or C30-C32; sufficient knowledge of German in spoken and written
Exclusion Criteria
non-existent consent, emergency patients, patients younger than 18 years of study, patients with intellectual disability (ICD-10 F70-F79), dementia, Alzheimer's disease
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method EORTC QLQ-C30 (subscale fatigue, general health and quality of life, gastrointestinal side effects);<br><br>Data collection: using a tablet-based patient survey and digital doctor checklist;<br><br>time of measurement: before the start of therapy, after completion of the primary therapy, directly after radiotherapy, 3, 6, 9 12 and 15 months after irradiation;<br><br>The study aims to assess the functional ability, symptom burden and quality of life as a function of tumor stage and therapy by means of interactive systems in the routine practical care of patients with head and neck cancer.
- Secondary Outcome Measures
Name Time Method Pain, GAD-2, PHQ-9, social score, rehabilitation needs, EAT-10, survival