Isovolumetric and Isocaloric Preloads of Various Types of Milk on Food Intake, Subjective Appetite and Glycemic Response
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ClinicalTrials.gov Identifier: NCT01025557 |
Recruitment Status :
Completed
First Posted : December 3, 2009
Last Update Posted : June 14, 2012
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Diabetes Prevention Obesity Prevention | Other: Dietary intervention | Phase 1 Phase 2 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 52 participants |
Allocation: | Randomized |
Intervention Model: | Crossover Assignment |
Masking: | Single (Investigator) |
Primary Purpose: | Basic Science |
Official Title: | The Effects of Isovolumetric and Isocaloric Preloads of Various Types of Milk on Food Intake, Subjective Appetite and Glycemic Response in Healthy Young Men and Women |
Study Start Date : | September 2009 |
Actual Primary Completion Date : | June 2011 |
Actual Study Completion Date : | May 2012 |
Arm | Intervention/treatment |
---|---|
Experimental: Chocolate milk |
Other: Dietary intervention
Dietary treatments with beverages |
Experimental: Milk |
Other: Dietary intervention
Dietary treatments with beverages |
Experimental: Infant formula |
Other: Dietary intervention
Dietary treatments with beverages |
Experimental: Soy beverage |
Other: Dietary intervention
Dietary treatments with beverages |
Experimental: Water |
Other: Dietary intervention
Dietary treatments with beverages |
- Food intake [ Time Frame: 30 minute ]
- Blood glucose [ Time Frame: 0, 10, 20, 30, 50, 80, 110, 140 and 170 minutes ]

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Ages Eligible for Study: | 20 Years to 30 Years (Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Healthy
- Non-smoking
- Aged 20-30 years
- Body mass index between 20 and 24.9 kg/m2
Exclusion Criteria:
- Diabetes
- Medication
- Lactose-intolerance or allergies to milk
- Breakfast skippers and those on an energy restricted diet

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01025557
Canada, Ontario | |
University of Toronto | |
Toronto, Ontario, Canada, M5S 3E2 |
Principal Investigator: | Harvey Anderson, Ph.D. | University of Toronto |
Responsible Party: | G. Harvey Anderson, Professor, University of Toronto |
ClinicalTrials.gov Identifier: | NCT01025557 |
Other Study ID Numbers: |
Milk Study - Experiment 1 DFO_24235 |
First Posted: | December 3, 2009 Key Record Dates |
Last Update Posted: | June 14, 2012 |
Last Verified: | June 2012 |
Food intake Blood glucose Milk |