- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02014220
The Food Intake, Satiety and Blood Glucose After Ingestion of Potato Chips Produced From Three Potato Cultivars
December 11, 2013 updated by: G. Harvey Anderson, University of Toronto
Potato is one of the world's most popular foods and is widely accepted as a staple food.
The objective of this study is to determine the effect of consuming potato chips from different cultivars on blood glucose, subjective appetite and food intake.
It is hypothesized that the chips produced from various potato cultivars will differ in their effect on blood glucose, satiety and food intake.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
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
-
-
Ontario
-
Toronto, Ontario, Canada, M5S 3E2
- Department of Nutritional Sciences
-
-
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
18 years to 35 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Healthy men with a body mass index (kg/m2) of 20-24.9
Exclusion Criteria:
- smocking, medication, breakfast skipping, restrained eating
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: Prevention
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Atlantic Western chips
deep fried potato chips
|
|
Experimental: Dakota Pearl chips
deep fried potato chips
|
|
Experimental: Andover Ontario chips
deep fried potato chips
|
|
Experimental: white bread with margarine
energy control
|
|
Experimental: white bread
control
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
blood glucose
Time Frame: 120 min
|
Glycaemic response will be measured before the treatment (baseline) and at 15, 30, 45, 60, 90 and 120 min after the treatment.
The glucose concentration will be measured in capillary blood using portable glucose meter.
|
120 min
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
food intake
Time Frame: 120 min
|
Ad libidum food intake will be measure at 120 min using test pizza meal.
The amount of consumed test meal (g) will be converted to the energy (kcal).
|
120 min
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
satiety
Time Frame: 120 min
|
Subjective appetite will be measured with visual analogue scales at 0 min immediately before the treatment (baseline) and at 15, 30, 45, 60, 90 and 120 min after the treatment.
|
120 min
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
Primary Completion (Actual)
December 1, 2008
Study Registration Dates
First Submitted
December 8, 2013
First Submitted That Met QC Criteria
December 11, 2013
First Posted (Estimate)
December 18, 2013
Study Record Updates
Last Update Posted (Estimate)
December 18, 2013
Last Update Submitted That Met QC Criteria
December 11, 2013
Last Verified
December 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Potato study 3: cultivar chips
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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