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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01717703
Other study ID # REB 2009-020-001
Secondary ID
Status Completed
Phase N/A
First received October 23, 2012
Last updated October 29, 2012
Start date January 2010
Est. completion date January 2012

Study information

Verified date October 2012
Source Ryerson University
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

The purpose of this experiment was to describe the effect of consuming 350 ml of 1% chocolate milk 60 minutes before a pizza meal on subjective appetite and short-term food intake when compared to cola, a fruit drink and a water control in normal weight and overweight/obese 9-14 year old boys and girls. It is hypothesized that 1% chocolate milk will increase meal time satiation to a greater extent than other sugars-sweetened commercially available beverages. Food intake will be measured 60 minutes after the consumption of 350 ml of water, fruit drink, cola or 1% chocolate milk.


Recruitment information / eligibility

Status Completed
Enrollment 55
Est. completion date January 2012
Est. primary completion date January 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 9 Years to 14 Years
Eligibility Inclusion Criteria:

- healthy boys and girls 9-14 years of age, stable weight, born at full term, normal birth weight

Exclusion Criteria:

- restricted diet, taking medications that affect food intake, significant learning, behavioral or emotional problems, food allergies to test treatments

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Water

Fruit drink

Cola

1% chocolate milk


Locations

Country Name City State
Canada Department of Applied Human Nutrition Bedford Nova Scotia

Sponsors (2)

Lead Sponsor Collaborator
Ryerson University Mount Saint Vincent University

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Food intake (kcal) 60 min after the treatment No
Secondary Subjective appetite (in mm) Subjective appetite by visual analogue scale (mm) measured at 0, 15, 30, 45, 60 and 90 minutes. 0-90 min No
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