Our hypothesis is that the satiating capacity of protein is partly regulated via the savoury signal of foods. We therefore expect that the savoury diet is more satiating than the sweet diet and the control diet, resulting in a decreased intake after…
ID
Bron
Verkorte titel
Aandoening
Eating Behaviour
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Our main outcome measurement is the difference in energy intake (kJ) during an ad libitum test meal after 24h of a sweet diet, a savoury diet, and a control diet.
Achtergrond van het onderzoek
Rationale:
Sensory properties of food play an important role in food selection and intake. Within our food range, products containing high protein levels are in general more savoury, while products containing carbohydrates are generally more sweet. Protein has been found to be the more satiating macronutrient. The role of sensory signals in the satiating effects of protein, however, requires further clarification.
Objective:
To determine the effect of sensory signals on satiety and food preferences.
Study design:
The study will consists of three test days, which will be separated by 1 week. These test days involve consumption of pre-determined iso-caloric diets consisting of only sweet products (sweet diet), only savoury products (savoury diet) or a combination of sweet and savoury products (control diet), using a randomized crossover design. Afterward energy intake (kJ) of an ad libitum test meal is measured. In addition, during the test days, sensations of appetite and several measures of food preferences will be assessed.
Study population:
The study population will consist of 40 apparently healthy, unrestrained, non-smoking, volunteers between the age of 18 and 35 with a normal body weight.
Main study parameters/endpoints:
Our main outcome measurement is the difference in energy intake (kJ) during an ad libitum test meal after 24h of a sweet diet, a savoury diet, and a control diet.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness:
The study is non-therapeutic to the participants. The risk associated with participation is negligible and the burden can be considered as low. No invasive measurements are present.
Doel van het onderzoek
Our hypothesis is that the satiating capacity of protein is partly regulated via the savoury signal of foods. We therefore expect that the savoury diet is more satiating than the sweet diet and the control diet, resulting in a decreased intake after the savoury diet. In addition we expect that eating a savoury diet will shift food preferences to low-protein foods. We expect that the sweet diet will be less satiating than the control diet, and that this diet will shift food preferences to high-protein foods.
Onderzoeksopzet
Every participant will visit the laboratory every day during the test (in total 6 times).
Onderzoeksproduct en/of interventie
The study will consists of three test days, which will be separated by 1 week. These test days involve consumption of pre-determined iso-caloric diets consisting of only sweet products (sweet diet), only savoury products (savoury diet) or a combination of sweet and savoury products (control diet), using a randomized crossover design. Afterward energy intake (kJ) of an ad libitum test meal is measured. In addition, during the test days, sensations of appetite and several measures of food preferences will be assessed.
Publiek
Division of Human Nutrition<br>
PO Box 8129
S. Griffioen-Roose
Agrotechnion r.4004
Bomenweg 4
Wageningen 6700 HD
The Netherlands
+31 (0)317 485897
sanne.griffioen-roose@wur.nl
Wetenschappelijk
Division of Human Nutrition<br>
PO Box 8129
S. Griffioen-Roose
Agrotechnion r.4004
Bomenweg 4
Wageningen 6700 HD
The Netherlands
+31 (0)317 485897
sanne.griffioen-roose@wur.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Age: 18-35 years;
2. BMI: 18.5 – 25.0 kg/m2;
3. Healthy (as judged by the participant).
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Restraint eating (men: score > 2.25; women: score > 2.80);
2. Lack of appetite;
3. Having difficulties with swallowing/eating;
4. Usage of an energy restricted diet during the last two months;
5. Weight loss or weight gain of 5 kg or more during the last two months;
6. Stomach or bowel diseases;
7. Kidney disorders;
8. Diabetes, thyroid disease, other endocrine disorders;
9. Usage of daily medication other than birth control pills;
10. For women: Pregnant or lactating;
11. Smoking (at least one cigarette a day);
12. Being a vegetarian;
13. Being allergic/intolerant for products under study;
14. Having participated in studies that have used the LFPQ: ‘RiceTime’, ‘LunchTime’, ‘ProStudy’, and ‘ProTime’, or current participation in other research from the division of human nutrition (WUR).
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Register | ID |
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NTR-new | NL2737 |
NTR-old | NTR2875 |
Ander register | MEC Wageningen / ABR : 11/10 / NL36114.081.11; |
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