A Comparison of Beverages Consumed Within a Meal to Satiation on Meal-time Food Intake and Post-meal Appetite and Glycemic Response in Healthy Young Adults

Obesity Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01595919
• Other study ID #: Mixed Meal Milk Study
• Status: Completed
• Phase: N/A
• First received: May 8, 2012
• Last updated: June 14, 2012
• Start date: April 2011
• Est. completion date: December 2011

Study information

• Verified date: June 2012
• Source: University of Toronto
• Contact: n/a
• Is FDA regulated: No
• Health authority: Canada: Ethics Review Committee
• Study type: Interventional

Clinical Trial Summary

The objective of the current study is to determine the effects of an ad libitum intake of 1% milk, fruit juice, regular cola, diet cola and water, as part of a pizza meal, on meal food intake, appetite and postprandial blood glucose in healthy men and women. We hypothesize that 1% milk will reduce food intake and result in better post-meal glycemic response compared to the other beverages.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 26
• Est. completion date: December 2011
• Est. primary completion date: December 2011
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 20 Years to 30 Years

Eligibility

Inclusion Criteria:

• healthy men and women

• age 20-30 years

• BMI between 20-24.9 kg/m^2

Exclusion Criteria:

• breakfast skippers

• diabetes or any metabolic diseases

• lactose intolerance or allergies to milk

• taking medications

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Basic Science

Related Conditions & MeSH terms

• Hyperglycemia
• Obesity

Intervention

Other:
• Nutritional Intervention
Ad libitum amounts of beverage at a meal

Locations

Country	Name	City	State
Canada	University of Toronto, Department of Nutritional Sciences	Toronto	Ontario

Sponsors (1)

Lead Sponsor	Collaborator
University of Toronto

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Food Intake	Measurement of energy intake during an ad libitum test meal	2 hours	No