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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01996514
Other study ID # FoodAdsKids_21595
Secondary ID MOP-82728
Status Completed
Phase N/A
First received November 21, 2013
Last updated November 26, 2013
Start date November 2010

Study information

Verified date November 2013
Source University of Toronto
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

We hypothesized that FA in a TV program watched during a meal, would block satiety responses to pre-meal energy consumption and delay satiation in OW/OB but not in NW boys and girls. Food intake was measured at 30 min following a glucose (1 g of glucose/kg body weight) or sweetened noncaloric beverage with or without the presence of food advertisements. Subjective appetite will be measured as well.


Recruitment information / eligibility

Status Completed
Enrollment 59
Est. completion date
Est. primary completion date August 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 9 Years to 14 Years
Eligibility Inclusion Criteria:

- born at full-term and of normal birth weight with no emotional, behavioral or learning problems

Exclusion Criteria:

- emotional, behavioral or learning problems dieting

Study Design

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


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Glucose with water
Glucose (1.0 g•kg-1 body weight ) in 250 mL of water 30 min before meal
non-caloric sweetener with water
0.15 g of the high-intensity sweetener, Splenda sucralose in 250 mL of water 30 min before meal
Behavioral:
TV program with non-food advertisements while feeding
30 minutes of TV program containing non-food ads during a meal
TV program with food advertisements while feeding
30 minutes of TV program containing non-food ads during a meal

Locations

Country Name City State
Canada University of Toronto Toronto Ontario

Sponsors (2)

Lead Sponsor Collaborator
University of Toronto Canadian Institutes of Health Research (CIHR)

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Food intake at 30 min after treatment No
Secondary Subjective appetite 0 to 60 min No
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