- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02484625
The Effect of Dairy and Non-Dairy Snacks on Food Intake, Subjective Appetite in Children
September 16, 2020 updated by: Mount Saint Vincent University
The Effect of Solid, Semi-Solid and Fluid Dairy Products on Short-Term Food Intake and Satiety in Children
Dairy products have the potential to be healthy snack foods for children and are provided in a variety of food matrices.
For instance, milk represents a fluid product, yogurt can be classified as a semi-solid food, and finally, cheese is the example of solid food.
This experiment is aimed to examine the effect of dairy products with different food matrices on satiety and food intake in children.
Dairy products will be compared with other non-dairy snacks popular among children including cookies and potato chips.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
40
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Nova Scotia
-
Halifax, Nova Scotia, Canada, B3M 2J6
- Mount Saint Vincent University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
9 years to 14 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Born at full-term within the normal weight range
- 9-14 year old
Exclusion Criteria:
- Food sensitivities or allergies,
- Dietary restrictions,
- Health, learning, emotional or behavioural problems
- Receiving medication
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Potato chips
Commercial potato chips, 180 kcal
|
Commercially available potato chips, 180 kcal
|
Experimental: Greek yogurt
Greek yogurt, 180 kcal
|
Commercially available Greek yogurt, 180 kcal
|
Experimental: Cookies
Sandwich-type cookies, 180 kcal
|
Commercially available cookies, 180 kcal
|
Experimental: Cheese
Mozzarella cheese, 180 kcal
|
Commercially available cheese, 180 kcal
|
Experimental: Milk (fluid)
Milk, 2% m.f., 180 kcal
|
Commercially available milk, 180 kcal
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Food intake (grams and kcal) measured with a test meal
Time Frame: 120 min
|
The amount of energy (kcal) consumed ad libitum with the test meal (pizza lunch) two hours later.
|
120 min
|
Subjective appetite measured with Visual Analogue Scales
Time Frame: 0-120 min
|
The subjective assessment of appetite parameters including a desire to eat, fullness, hunger and a prospective food consumption measured with 100 mm Visual Analogue Scales with two opposite statements at each end (e.g., for the hunger scale, 0 mm means not hungry at all, and 100 mm means very hungry).
|
0-120 min
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Cortisol
Time Frame: 0-120 min
|
The concentration of salivary cortisol
|
0-120 min
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Bohdan L Luhovyy, PhD, Mount Saint Vincent University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 1, 2011
Primary Completion (Actual)
August 1, 2017
Study Completion (Actual)
August 1, 2017
Study Registration Dates
First Submitted
April 17, 2015
First Submitted That Met QC Criteria
June 26, 2015
First Posted (Estimate)
June 29, 2015
Study Record Updates
Last Update Posted (Actual)
September 18, 2020
Last Update Submitted That Met QC Criteria
September 16, 2020
Last Verified
September 1, 2020
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2011-001
- 2016-130 (Other Identifier: Mount Saint Vincent University)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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