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NCT01025687 Clinical Trial

Television Viewing (TVV) & Puberty on Lunchtime Food Intake

Obesity Prevention Clinical Trial

Official title:
Effect of Television Viewing (TVV) & Puberty on Lunchtime Food Intake & Subjective Appetite in Girls

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01025687
Other study ID # KidsStudy_21595
Secondary ID
Status Completed
Phase N/A
First received December 2, 2009
Last updated December 2, 2009
Start date February 2009
Est. completion date October 2009

Study information
Verified date December 2009
Source University of Toronto
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

The investigators hypothesize that television viewing will affect food intake in adolescent girls, and will depend on pubertal stage. Food intake will be measured at 30 min following a glucose(1 g of glucose/kg body weight) or sweetened noncaloric beverage with or without the presence of TV. Subjective appetite will be measured as well.

Recruitment information / eligibility
Status Completed
Enrollment 25
Est. completion date October 2009
Est. primary completion date September 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 9 Years to 14 Years
Eligibility Inclusion Criteria:

- healthy girls with no emotional, behavioral or learning problems

Exclusion Criteria:

- boys

Study Design

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

Related Conditions & MeSH terms

Intervention

Dietary Supplement:
• water with noncalorie sweetener

• water with glucose

Behavioral:
• TV program showed while feeding

• TV program showed while feeding

Locations
Country Name City State
Canada Department of Nutritional Sciences 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 (kcal) at 30 min after the treatment No
Secondary subjective appetite 0-120 min No
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