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Physical Activity Program and Energy Intake Control in Obese Adolescents

Not Applicable
Conditions
Pediatric Obesity
Interventions
Behavioral: Physical activity intervention
Registration Number
NCT02482220
Lead Sponsor
Université Blaise Pascal, Clermont-Ferrand
Brief Summary

Acute exercise of high intensity has been shown to induced nutritional adaptations in obese adolescents. Indeed, several studies have shown that about 30 minutes of intensive exercise (above 70% of the adolescents maximal aerobic capacities) can favor reduced-energy consumption at the following meal with no modification of their appetite feelings. Although it is suggested that chronic physical activity programs can induce energy intake modifications, this has never been clearly studied. The aim of this work is to compare different physical activity programs (low vs. high intensity programs) in terms of energy intake, appetite feelings and appetite-regulating hormones, in obese adolescents.

Detailed Description

After an first medical visit to ensure that the adolescents have the ability to complete the whole study, the participants will have to complete several clinical examinations:

* anthropometric measurements

* Body composition assessed by DXA

* Maximal aerobic test

* Blood samples (appetite-regulating hormones)

* daily energy intake assessment during a 24h intake exploration.

The adolescents recruited will then be randomly assigned to one of the two intervention groups:

- High Intensity program or moderate intensity program. Those two physical activity programs will last 4-months and will be composed of 3 to 4 exercise sessions per week. The High intensity program will consists in High intensity interval exercises starting at 70% of the adolescents' capacities at the beginning to end around 95%. The moderate intensity program will propose continuous exercises set between 50-65% VO2max.

No energy intake intervention will be performed.

By the end of the 4-months intervention, all the clinical examinations performed before the intervention will be repeated.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
70
Inclusion Criteria
  • 12 to 15 years old adolescents
  • Obese according to international values for BMI
  • Being registered to the national social security insurance
  • no eating disorders
  • no medications
  • metabolic disorders
Exclusion Criteria
  • metabolic disorders
  • food disorders
  • physical disability

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Moderate intensityPhysical activity interventionin this group, the participants will follow a moderate intensity physical activity program (Intensity from 50 to 65% VO2max)
High intensityPhysical activity interventionin this group, the participants will follow a high intensity physical activity program (High Intensity Interval exercise from 75 to 95% VO2max)
Primary Outcome Measures
NameTimeMethod
change in Energy intake in kcal is being assessedenergy intake will be assessed during 24h during the week before the intervention (T0) and the week after (T1)

daily energy intake will be assessed

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

AME2P Laboratory

🇫🇷

Clermont-ferrand, Auvergne, France

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