Appetite Regulation Clinical Trial
Official title:
The Effect of Meal Replacement Bars Containing Different Types of Fibres (Oligofructose and/or Barley) on Satiety and Energy Intake
The effect of beta-glucan or fructo-oligosaccharide or their combination in bars on satiety and food intake was tested by supplying these bars on two consecutive days.
Status | Completed |
Enrollment | 24 |
Est. completion date | April 2007 |
Est. primary completion date | March 2007 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 60 Years |
Eligibility |
Inclusion Criteria: - Age at start of the study 18 till 60 years - Quetelet-Index (BMI) from 21 till 32 kg/m2 inclusive - 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, macro-biotic or biologic dynamic food habits - No Fibre supplements (only once a day) - No blood donations during the study. - Reported intense sporting activities less than 10h/w - Reported alcohol consumption less than 21 units/w (female volunteers) or less than 28 units/w (male volunteers) - Having a General Practitioner - Informed consent signed - Recruitment form filled out Exclusion Criteria: - Smoking - Dislike, allergy/intolerance or not known with the foods of the ad libitum meal - Possible eating disorder (measured by SCOFF questionnaire) - High or very high restrained eaters (measured by questionnaire) (men with BMI < 27: restraint score > 2.37, men with BMI less than 27: restraint score > 3.04, women with BMI < 26: restraint score > 3.24, women with BMI less than 26: restraint score > 3.41) - Reported medical treatment that may affect eating habits/satiety - Reported intolerance or allergy to test products - Women reported lactating (or lactating < 6 weeks ago), pregnant (or pregnant < 3 months ago) or wish to become pregnant during the study - Reported weight loss/gain (10%) in the last six month before the trial - Reported participation in another biomedical trial 1 month before the start of the study - Reported working on late turns - |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor)
Country | Name | City | State |
---|---|---|---|
Netherlands | Unilever R&D Vlaardingen | Vlaardingen |
Lead Sponsor | Collaborator |
---|---|
Unilever R&D |
Netherlands,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Satiety and food intake | 2 days each week for 4 weeks | No |
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