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Impact of active video game on adolescent health

Not Applicable
Conditions
Obesity
Registration Number
RBR-2xn3g6
Lead Sponsor
niversidade Estadual da Paraíba
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

To be enrolled and attending the classes from the 5th to the 9th year of the public school network of the urban area of ??Campina Grande-PB selected for the study; being in the age group of 10 to 18 years; have nutritional status characterized as being overweight or obese.

Exclusion Criteria

Present some motor (although temporary) or mental limitation that impedes the participation in the activities of the intervention and / or the accomplishment of the exams, as the pulmonary function tests; have any severe metabolic changes that require the use of medications or specific treatment that alter the metabolism of the lipid profile; have asthma with a recent crisis (two months prior to data collection) and / or report of exercise-induced bronchospasm; not being, at the time of the research, overweight treatment, and active video game users;
for women, being pregnant or breastfeeding.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improvement of cardiorespiratory function: measured by heart rate (measured by heart monitor) and by pulmonary function (through inspiratory and expiratory pressure, frequency, spirometry and manuvacometry), with expected effect of 0.6 points for each outcome. Data will be collected 2 weeks before and 1 week after the intervention.
Secondary Outcome Measures
NameTimeMethod
Improvement of macrocirculation: assessed by carotid doppler.<br>Improvement of the microcirculation, evaluated by maximum and resting blood flows, using the Laser Doppler flowmetry technique<br>(LDF) with the VMS-LDF® device (Moor Instruments, UK) with dual flow channel.<br>Nutritional status: assessed by body mass index, determined by weight ratio divided by the square of height.<br>Dyslipidemia: evaluated through biochemical markers for total cholesterol and fractions, and triglycerides, determined by colorimetric technique.<br>Blood pressure: measured by tensiometer.<br>For all parameters, the expected effect is 0.6 points. Data collected 2 weeks before and 1 week after the intervention.
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