Exercise-snacks for Breaking the Sedentary Lifestyle and Improving the Physical Fitness of Obese Adolescents?

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age11-18
SponsorUniversity of Avignon

About this trial

The management of a person with obesity involves long-term behavioral changes with a balanced diet in both quantity and quality, along with the adoption of a more active lifestyle: increasing physical activities and reducing sedentary behaviors. The school setting has been identified as a favorable environment for interventions aimed at reducing and interrupting the time adolescents spend sitting and preventing the associated negative health consequences.

Recently, very short (\< 1 minute) and intense exercises, called 'exercise-snacks,' have been reported to be effective in adults for 1) improving physical fitness over 6 weeks, and 2) improving vascular function and lowering blood glucose levels over a single day. Additionally, in adolescents with diabetes, they have been shown to reduce body fat. This raises the question of whether adding \'exercise-snack\' sessions to a multidimensional care program for hospitalized obese adolescents could further improve their physical fitness in the short and medium term.

The objective of this project is to compare the effects of a traditional multidimensional care program with the addition of 'exercise-snacks' to the same care program without \'exercise-snacks\' on the physical fitness, body composition, vascular function, and physical activity and sedentary behaviors of obese children in the short and medium term. Forty-eight obese adolescents will be included. The \'exercise-snack\' group will perform six exercise sessions per day for three weeks in addition to the standard care. The control group will receive only the standard care. Assessments of physical fitness, body composition, vascular health, and questionnaires on physical activity, sedentary behavior, and cognitive restraint will be conducted at the beginning and end of the three-week program, as well as 1 and 3 months after the end of the program.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Body mass index Z-score corresponding to stage 2 obesity,

no weight loss of more than 5% of total body weight in the past 3 months,

parental consent

minor's acceptance

Disqualifiers

Contraindication to physical activity

current participation in a clinical trial

Trial design

Design model

Parallel

Treatments tested in this trial

  • exercise-snack group

    Other intervention

    Adolescents in the exercise-snacks group will perform 4 \"exercise-snacks\" sessions per day during 3 weeks in addition to multidimensional care program. These sessions will consist of 1-min various intense supervised exercises . They will also receive information about their attitudes to physical activity.

Treatment groups

48 Participants
are divided into 2 treatment groups
Group A: exercise-snack groupExperimental treatment 1 intervention
Group B: control groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Changes in aerobic fitness: predicted VO2max

Measured by the Spartacus 15-15 field test, an intermittent maximal running field test with prediction of VO2max: For girls: VO2max = last stage \* 153.4433 + BMI \* 58.64534 + âge \* -2.701522-921.2878 For boys: VO2max = last stage \* 153.4433 + 320.1583 + BMI \* 58.64534 + âge \* -2.701522-921.2878

Time frame
at inclusion, at the end of the 3-weeks program and 1 and 3 month following the end of the program

Secondary outcomes

1

Changes in fat mass

measured by medical body composition analyzer mBCA SECA, in kg

Time frame
from inclusion to the end of the 3-weeks program and 1 and 3 month following the end of the program
2

Changes in body mass index in kg/m²

Time frame
at inclusion, at the end of the 3-weeks program and 1 and 3 month following the end of the program
3

change in carotid extra-media thickness

measured by echocardiography (Mylab, Esaote, Italie) and off-line analyses by CAROLAB, in mm

Time frame
at inclusion, at the end of the 3-weeks program and 1 and 3 month following the end of the program
4

Changes in carotid intima-thickness

measured by echocardiography (Mylab, Esaote, Italie) and off-line analyses by CAROLAB, in mm

Time frame
at inclusion, at the end of the 3-weeks program and 1 and 3 month following the end of the program

Other outcomes

Sponsors and contacts

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University of Avignon

Lead sponsor

Institut Saint Pierre

Collaborator