Acute Effect of Cheeses With Different Energy Content on Appetite
NCT ID: NCT02582723
Last Updated: 2016-02-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
40 participants
INTERVENTIONAL
2015-09-30
2015-11-30
Brief Summary
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Detailed Description
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Once settled into an individual feeding cubicle, visual analogue scales (VAS) will be completed for the measurement of fasting appetite levels. A standardized fixed breakfast meal (providing approximately 20% of total estimated energy need) consisting of 80 g. cheese with bread, orange juice and a cup (125 mL) of coffee/the/water (milk is not allowed). The amounts of bread (70.5 g.) and juice (132 g.) are calculated with Babybel original as reference, and these amounts for bread and juice are kept constant regardless of the cheese provided. The cheese will be served blinded together with the bread, and the brand of cheese will not be mentioned for the participants. Participants will be asked to consume this breakfast within 15 minutes and the exact meal duration (in minutes) will be noted after completing the meal in order to examine the eating rate. VAS will be used to measure subjective appetite sensations during the post-meal period as well as the pleasantness of the meal and the study products after completing the meal. VAS will be used to measure subjective appetite sensations for the following hours. Three hours following serving of the breakfast meal, participants will be provided with a homogeneous single item ad libitum lunch meal. The meal is a homogeneous dish of spaghetti bolognese providing a total of 8 MJ and the participants are instructed to eat until they are comfortably full. The energy composition of the meal is 15 E% protein, 30 E% fat and 55 E% carbohydrate. VAS will be used to measure subjective appetite sensations during the post-meal period as well as the pleasantness of the meal after completing the meal. The meal duration (in minutes) will be noted after completing the meal. The ad libitum meal ends the study day, and the participant will be free to leave afterwards.
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
QUADRUPLE
Study Groups
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High protein/high fat hard cheese
Served for breakfast together with bread, juice and coffee, tea or water
High protein/high fat hard cheese
Assess whether the cheeses with high protein content have improved effect on satiety compared to the cheese with low protein content.
High protein/low fat hard cheese
Served for breakfast together with bread, juice and coffee, tea or water
High protein/low fat hard cheese
Assess whether the cheeses with high protein content have improved effect on satiety compared to the cheese with low protein content.
Low protein/high fat creme cheese
Served for breakfast together with bread, juice and coffee, tea or water
Low protein/high fat creme cheese
Assess whether the cheeses with high protein content have improved effect on satiety compared to the cheese with low protein content.
Interventions
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High protein/high fat hard cheese
Assess whether the cheeses with high protein content have improved effect on satiety compared to the cheese with low protein content.
High protein/low fat hard cheese
Assess whether the cheeses with high protein content have improved effect on satiety compared to the cheese with low protein content.
Low protein/high fat creme cheese
Assess whether the cheeses with high protein content have improved effect on satiety compared to the cheese with low protein content.
Eligibility Criteria
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Inclusion Criteria
* Healthy men and women
* Ages between 18 and 60 years
* BMI between 20.0-31.9 kg/m2
* Regular breakfast eaters (eating breakfast ≥ 4 times a week)
* Regular menstrual periods (women only)
Exclusion Criteria
* Significant health problems as judged by the investigator
* Taking any medication or supplements known to affect appetite or body weight within the past month and/or during the study as judged by the investigator
* Pregnant, planning to become pregnant within the next 4 weeks or breastfeeding (women only)
* History of anaphylaxis to food
* Any known food allergies or food intolerance likely to affect the present study
* Smoking, smoking cessation within the past 3 months or nicotine use (electronic cigarettes)
* Self-reporting currently dieting or having lost/gained significant amount of weight (±3 kg) in the previous 3 months
* Significant changes in physical activity patterns in the past 4 weeks or intention to change during the study as judged by the investigator
* Significant change in diet in the past 4 weeks or intention to change the diet during the study as judged by the investigator
* Use of systemic or local treatment likely to interfere with evaluation of the study parameters as judged by the investigator
* Participants who work in appetite or feeding related areas
* Post-menopausal (women only)
18 Years
60 Years
ALL
Yes
Sponsors
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Fromageries Bel SA
INDUSTRY
University of Copenhagen
OTHER
Responsible Party
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Arne Astrup
Professor
Principal Investigators
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Arne Astrup, Professor
Role: STUDY_CHAIR
University of Copenhagen
Locations
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University of Copenhagen
Copenhagen, , Denmark
Countries
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Other Identifiers
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B323
Identifier Type: -
Identifier Source: org_study_id
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