Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
NCT07258589

The TASTY-training Study

Led by University Medical Center Groningen · Updated on 2025-12-02

90

Participants Needed

11

Research Sites

137 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

A multicentre non-blinded randomised intervention trial with a parallel cluster design. The multicentre study will be performed at 12 hospitals in the Netherlands. A parallel cluster design per hospital was selected to prevent contact between participants in the same hospital who are randomised into different study arms. Such contact may result in bias as it may allow for patients in the control arm to be informed about elements of taste and smell training. To examine the effect of at-home taste and smell training versus standard care on taste function and other outcome parameters, measurements will take place at baseline (before the training starts), and after 12 weeks. The intervention will take place at home. The control group will receive usual care. Questionnaires will be filled in online at home, while taste and smell tests and saliva collection will be conducted either at home or in the hospital during regular visits. Patients in both study arms are contacted by their dietitian every 3 weeks.

CONDITIONS

Official Title

The TASTY-training Study

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 to 70 years
  • Plan to be treated with tyrosine kinase inhibitors for the next 12 weeks
  • Experiencing taste changes after starting tyrosine kinase inhibitors
  • Able to consume solid foods and drinks
  • At most 50% of daily calories from oral nutritional supplements
  • Oral mucositis grade 2 or lower (per Common Terminology Criteria for Adverse Events v5.0)
  • Able to follow all study procedures
  • Provided written informed consent
Not Eligible

You will not qualify if you...

  • Currently pregnant
  • History of taste, smell, or saliva problems before tyrosine kinase inhibitor treatment
  • Past or current radiotherapy in head and neck area
  • Receiving tube feeding or intravenous nutrition
  • Participating in another clinical trial targeting taste or smell changes
  • Using high-dose corticosteroids for more than 1 month (over 10 mg prednisone daily or equivalent)

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 11 locations

1

Amsterdam UMC

Amsterdam, Netherlands

Actively Recruiting

2

Rijnstate Ziekenhuis

Arnhem, Netherlands

Not Yet Recruiting

3

Van Weel-Bethesda Ziekenhuis

Dirksland, Netherlands

Not Yet Recruiting

4

Ziekenhuisvoorzieningen Gelderse Vallei

Ede, Netherlands

Actively Recruiting

5

University Medical Center Groningen

Groningen, Netherlands, 9713 GZ

Actively Recruiting

6

Martini Ziekenhuis

Groningen, Netherlands

Actively Recruiting

7

Radboud University medical Center

Nijmegen, Netherlands

Not Yet Recruiting

8

Ikazia Ziekenhuis

Rotterdam, Netherlands

Actively Recruiting

9

Ommelander Ziekenhuis Groningen

Scheemda, Netherlands

Actively Recruiting

10

Maxima Medisch Centrum

Veldhoven, Netherlands

Not Yet Recruiting

11

Isala Klinieken

Zwolle, Netherlands

Not Yet Recruiting

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Research Team

J

J. J.A. de Haan, MD, PhD

CONTACT

M

M. D. Douma

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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