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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: Netherlands Trial Register
Last refreshed on: 28 April 2013
Main ID:  NTR1752
Date of registration: 30/03/2009
Primary sponsor: Wageningen University, Division of Human Nutrition
Public title: Effect of taste on sensory specific satiety.
Scientific title: Effect of taste on sensory specific satiety. - LunchTime
Date of first enrolment: 18/3/2009
Target sample size: 60
Recruitment status: complete
URL:  http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=1752
Study type:  intervention
Study design:  Randomised: Yes; Masking: None; Control: Not applicable; Group: Crossover; Type: 2 or more arms, randomized  
Countries of recruitment
The Netherlands
Contacts
Name: S.  Griffioen-Roose
Address:  Wageningen University Division of Human Nutrition PO Box 8129, Agrotechnion r.4004 Bomenweg 4 6700 HD Wageningen The Netherlands
Telephone: +31 (0)317 485897
Email: sanne.griffioen-roose@wur.nl
Affiliation: 
Name: S.  Griffioen-Roose
Address:  Wageningen University Division of Human Nutrition PO Box 8129, Agrotechnion r.4004 Bomenweg 4 6700 HD Wageningen The Netherlands
Telephone: +31 (0)317 485897
Email: sanne.griffioen-roose@wur.nl
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: 1. Age: 18-35 year;

2. BMI: 18.5 ¨C 25.0 kg/m2;

3. Healthy (as judged by the participant);

4. Liking for test products (assessed in screening-questionnaire with a 9-point hedonic scale, subjects have to like or have a neutral attitude towards the products: score ¡Ý 5).

Exclusion criteria: 1. Restraint eating (men: score > 2.25; women: score > 2.80) [13];

2. Lack of appetite for any (unknown) reason;

3. Usage of a energy restricted diet during the last two months;

4. Weight loss or weight gain of 5 kg or more during the last two months;

5. Stomach or bowel diseases;

6. Diabetes, thyroid disease, or any other endocrine disorder;

7. Having difficulties with swallowing/eating;

8. Hypersensitivity (allergy and/or intolerance) for the food products under study;

9. Smoking (at least one cigarette a day);

10. For women: pregnant or lactating;

11. Being a vegetarian;

12. Having participated in ¡®RiceTime¡¯ or current participation in other research from the division of human nutrition (WUR).


Age minimum:
Age maximum:
Gender:
Health Condition(s) or Problem(s) studied
Eating behaviour

Intervention(s)
Lunchmeal, either with a sweet or savoury flavour.
Primary Outcome(s)
Our main outcome measures of the different test-conditions are: The difference in habituation (responses) during the sweet and savoury meal (test-condition 1), the difference in motivation after a sweet or savoury meal to work for a certain food (test-condition 2) and the differences in different aspects of food choice after eating a sweet or savoury meal (test-condition 3). Agreements on the outcomes of the different methodologies used in the three test-conditions are assessed.
Secondary Outcome(s)
To assess ad libitum intake in all the test-conditions.
Secondary ID(s)
08/25 / 25900.081.08
Source(s) of Monetary Support
Technologiestichting STW (Stichting Technische Wetenschappen)
Secondary Sponsor(s)
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