C32 C10 C13
Conditions
Interventions
Group 1: App-based daily symptom control and weekly physician appointments.
Group 2: Weekly physician appointments.
Sponsors
Universitätsklinikum Freiburg
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: Indication for radiotherapy for head-and-neck cancers
Exclusion criteria
Exclusion criteria: Inability to consent to participation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Feasibility (80% of questions answered by 80% of patients) | — |
Secondary
| Measure | Time frame |
|---|---|
| Patient satisfaction (PSQ18) Quality of life (EORTC QLQ-C30, H&N35) Questionnaires prior to treatment initiation, at completion and during follow-up (months 3, 6, 9, 12, 18, 24 after treatment completion). | — |
Countries
Germany
Contacts
Public ContactNils Nicolay
Universitätsklinikum Freiburg, Klinik für Strahlenheilkunde
Outcome results
None listed