C00-C97
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - patients undergoing chemotherapy (tumor localisation: breast, lung, esophagus, pancreas, stomach and intestine) - age = 18 years - prior written consent
Exclusion criteria
Exclusion criteria: - presence of a genetic metabolic disorder - treatment/ previous treatment of an eating disorder (anorexia, bulimia, binge eating) - parenteral nutrition or supplemental enteral nutrition (food via PEG or PEJ, high calorie drinking food such as Fresubin or Fortimel) undergoing therapy for tumor cachexia - irradiation in the head/ neck area - pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the improvement of objective taste by clinically relevant 2 taste strip points in at least 50% of the patients of the intervention group | — |
Secondary
| Measure | Time frame |
|---|---|
| - Improvement of the objective taste category "salty", "sweet", "sour" and "bitter" (measured by taste strip) - Improvement of subjective taste perception (measured by anamnesis sheet of Prof. T. Hummel) - Feasibility and acceptance of taste and smell training - Recording the quality of life of all study patients | — |
Countries
Germany
Contacts
Universitäres Cancer Center Hamburg (UCCH)Hubertus Wald Tumorzentrum