Appetite Clinical Trial
Official title:
Effect of Liquid Volume and the Amount of Incorporated Gas Into a Carbohydrate/Protein Beverage on Satiety: a Response-surface-model Study
Verified date | April 2015 |
Source | Unilever R&D |
Contact | n/a |
Is FDA regulated | No |
Health authority | UK: Ethics committee |
Study type | Interventional |
Liquid foams can be formed by trapping pockets of gas in a beverage. The primary objective of this study is to test the individual contribution, and possible interaction, of the liquid volume and gas to liquid volume ratio (i.e. %overrun (%OR, defined as 100 x [gas volume/liquid volume]) of a beverage to its satiating properties.
Status | Completed |
Enrollment | 96 |
Est. completion date | February 2011 |
Est. primary completion date | February 2011 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 60 Years |
Eligibility |
Inclusion Criteria: - BMI between 21 and 32 kg/m² - Apparently healthy: measured by questionnaire: no reported current or previous metabolic diseases or chronic gastrointestinal disorders - Reported dietary habits: no medically prescribed diet, no slimming diet, used to eat 3 meals a day, no vegetarian. - Reported intense sporting activities below 10h/w - Reported alcohol consumption below 14 units/w (female volunteers) or below 21 units/w (male volunteers) Exclusion Criteria: - Dislike, allergy or intolerance to test products or indicating to be unable to consume 514 ml of aerated test product - Any food allergy, or dislike or intolerance with the foods supplied during the study - Eating disorder (measured by SCOFF questionnaire, 2 or more"yes" responses) High or very high restrained eaters (measured by questionnaire; score of 15 or higher, Polivy et al. 1978) - Reported medical treatment that may affect eating habits/satiety - Reported lactating (or lactating < 6 weeks ago), pregnant (or pregnant < 6 months ago) or wish to become pregnant during the study |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Basic Science
Country | Name | City | State |
---|---|---|---|
United Kingdom | Leatherhead Food Research | Leatherhead | Surrey |
Lead Sponsor | Collaborator |
---|---|
Unilever R&D |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Hunger and satiety questions (Area under the time curve of hunger and satiety scores (as rated by the subjects on a Visual Analog Scale) | Area under the time curve of hunger and satiety scores (as rated by the subjects on a Visual Analog Scale) | 245 minutes | No |
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