cancer malignancy cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: * Age >=18 and
Exclusion criteria
Exclusion criteria: - Pregnancy * History of taste, smell, or saliva production dysfunction before treatment with tyrosine kinase inhibitors - Previous or current radiotherapy of head and neck region - Enteral feeding through tube or parenteral feeding - Participation in another clinical trial aimed at preventing or treating taste and/or smell alterations - Chronic (>1 month) high dose corticosteroids (>10 mg prednisone/day or equivalent)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Taste functioning measured with Taste Strips at baseline and at 12 weeks of taste and smell training compared with standard care. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) Smell function measured with Sniffin sticks 2) Food enjoyment and food liking measured with AHSP and 9-point hedonic scale evaluation questionnaire 3) Quality of life: EORTC QLQ-C30; 4) Taste and smell alterations: Chemotherapy-induced Taste Alteration Scale (ciTAS-NL) 5) Risk of malnutrition: Patient-Generated Subjective Global Assessment (PG-SGA) 6) Dry mouth feeling: Xerostomia Inventory (XI) and Regional Oral Dryness Inventory (RODI) 7) Taste and smell function; taste strips and smell sticks 8) Saliva secretion and composition 9) Body weight. | — |
Countries
Netherlands
Contacts
Universitair Medisch Centrum Groningen