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NCT02119208 Clinical Trial

Effects of the Intensity and the Timing of the Physical Activity in a Primary School

Energy Intake Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT02119208
Other study ID # 13-135-CERES-P
Secondary ID
Status Not yet recruiting
Phase N/A
First received February 23, 2014
Last updated April 16, 2014
Start date May 2014
Est. completion date May 2014

Study information
Verified date April 2014
Source Université de Montréal
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

1. In natural environment, the moderate-intensity break will allow a reduction of the caloric intake at the dinner more important than for the light-intensity break

2. In natural environment, the break taken juste before dinner will allow a reduction of the caloric intake at the diner more important than earlier in the day.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 30
Est. completion date May 2014
Est. primary completion date May 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 4 Years to 6 Years
Eligibility Inclusion Criteria:

- Children aged of approximately 5 years old of a of a nursery class of the school Jacques-Barclay, St-Mathieu

Exclusion Criteria:

- Present allergy of the foods in the lunch

- having a handicap or a limitation that avoid walking, running or tkaing part of the physcial activity courses at the school.

- Having a potential surgery

- Having a metabolic disease or taking drugs that could have an impact on the results of the study

- Be vegetarian

- Having intestinal disorders

Study Design

Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention

Related Conditions & MeSH terms

Intervention

Behavioral:
• Intensity and timing of exercise

Locations
Country Name City State
Canada École Jacques-Barclay St-Mathieu Quebec

Sponsors (1)
Lead Sponsor Collaborator
Université de Montréal

Country where clinical trial is conducted

Canada, 

Outcome
Type Measure Description Time frame Safety issue
Primary Caloric intake at the breakfast, lunch and diner (kj) 3 days per condition Yes
Secondary Anthropometric measures At preliminary visit Yes
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