C01 C02 C04 C05 C06 C09 C10 C11 C12 C13 C14 C32
Conditions
Interventions
Group 1: Overall we want to include 200 patients with head and neck cancer. At least half of the patients should have a tumour stage III or IV (according to the UICC-classification version 8) or a sit
Sponsors
HNO-Klinik Universitätsklinikum Erlangen
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: Sufficient cognitive and language skills in order to understand the content of the questionnaires, a written informed consent of the patient after detailed information about the study, body weight of 50-120 kg.
Exclusion criteria
Exclusion criteria: Patients, who refuse to participate in the study or do not sign the informed consent, patients with cognitive impairments or language barriers, who are not able to understand the content of the questionnaires.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Survey of the symptom burden according to the 10 most common symptoms in patients with head and neck cancer. Analysis of the quality of life (German version of the "University of Washington Quality of Life Questionnaire (UW-QOL)") in head and neck tumour patients. | — |
Secondary
| Measure | Time frame |
|---|---|
| Detection of clinical, therapeutic and sociodemographic influencing factors. Palliative supply requirements according to the overall-score of the MIDOS(2)-questionnaire. Correlation between stage of disease and palliative care needs. | — |
Countries
Germany
Contacts
Public ContactAntoniu-Oreste Gostian
HNO-Klinik Universitätsklinikum Erlangen
Outcome results
None listed