- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04418713
Active Videogames Against Obesity in Children (VIDEOACTIVO)
Active Video Games Against Obesity and Sedentarism in Children Between 9 and 11 Years Old: a Disruptive Proposal
Active video games are presented as an exercise option for children with little interest in traditional sports. The main objectives of this study are:
- To evaluate the effects of an active video game program on cardiometabolic risk in overweight/obese children
- to identify the effect of this intervention on physical fitness
- to study possible changes in the sedentary lifestyles of children after the exercise program.
This is a randomized crossover study, with 2 intervention periods of 9 months each, and a 3-month period of washing. Ninetytwo children between 9 and 11 years old who are overweight or obese will be included and randomly assigned to one of the 2 homogeneous groups (control-intervention). Both groups will receive education in healthy lifestyles, and the intervention group will also follow a physical exercise program with active video games (3-4 days/week). The sessions will last between 30 and 45 minutes and will include different moderate-vigorous aerobic activities and muscular strength exercises. Body composition, physical fitness, levels of leptin, adiponectin and visfatin, lipid and ferric profiles, and markers of inflammation and metabolic risk such as insulin resistance, TNF-α, CRP, ALT, AST, gamma-GT and IL-6will be measured before and after the intervention. In addition, dietary habits (24h recalls), physical activity (accelerometers), blood pressure, waist and neck circumference, and pubertal development will be also assessed.
Study Overview
Status
Intervention / Treatment
Detailed Description
Childhood obesity is one of the main problems in developed societies, and entails enormous expenditure for the National Health System. In addition, childhood obesity is strongly associated with adult obesity and with all types of cardiovascular and metabolic pathologies. Physical exercise has been shown to be the great non-pharmacological enemy of both childhood and adult obesity, however sport practice and adherence to it is not easy in the overweight/obese population. In this context, active video games are presented as an exercise option for children with little interest in traditional sports. The main objectives of this study are: (1) To evaluate the effects of an active video game program on cardiometabolic risk in overweight/obese children; (2) to identify the effect of this intervention on physical fitness and (3) to study possible changes in the sedentary lifestyles of children after the exercise program.
This is a randomized crossover study, with 2 intervention periods of 9 months each, and a 3-month period of washing. Ninetytwo children between 9 and 11 years old who are overweight or obese will be included and randomly assigned to one of the 2 homogeneous groups (control-intervention). Both groups will receive education in healthy lifestyles, and the intervention group will also follow a physical exercise program with active video games (3-4 days/week). The sessions will last between 30 and 45 minutes and will include different moderate-vigorous aerobic activities and muscular strength exercises. Body composition, physical fitness, levels of leptin, adiponectin and visfatin, lipid and ferric profiles, and markers of inflammation and metabolic risk such as insulin resistance, TNF-α, CRP, ALT, AST, gamma-GT and IL-6will be measured before and after the intervention. In addition, dietary habits (24h recalls), physical activity (accelerometers), blood pressure, waist and neck circumference, and pubertal development will be also assessed.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Zaragoza, Spain, 50009
- José Antonio Casajús Mallén
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- children with obesity and overweight
- children with ages between 9-11 years old
- children in tanner stage I ó II
Exclusion Criteria:
- to take drugs that can affect the measurements
- menarche in girls
- contraindications or pathologies associated with exercise
- regular attendance at extracurricular activities of high energy expenditure
- diet
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: exercise group with active video-games
exergaming exercise: A combination of traditional exercise and exercise through active video games performed 3 days a week for one hour during 7 months.
As well, it will be including some session about nutritional advice.
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An intervention with active video-games to increase physical activity and improve body composition
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No Intervention: control group
no physical intevention will be provided, but it will be included some sessions on nutritional advice.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in fat mass during 6 months evaluated by Dual energy X-ray absorptiometry
Time Frame: Change from baseline in fat mass at 6 months
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Fat mass is measured by dual X-ray photon absorptiometry (DXA) using the software and pediatric reference values (Hologic Explorer, Hologic Corp., Software Latest Version, Waltham, MA).
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Change from baseline in fat mass at 6 months
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Change in size during 6 months evaluated by a height rod to the nearest 0.1 cm (SECA 225, SECA, Hamburg, Germany).
Time Frame: Change from baseline in size at 6 months
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Height is measured with a height rod to the nearest 0.1 cm (SECA 225, SECA, Hamburg, Germany),
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Change from baseline in size at 6 months
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Change in size during 6 months evaluated by a 0.1 kg precision bascule (SECA 861, SECA, Hamburg, Germany)
Time Frame: Change from baseline in weight at 6 months
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Weight of the children is measured by a 0.1 kg precision bascule (SECA 861, SECA, Hamburg, Germany)
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Change from baseline in weight at 6 months
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Change in waist and hip circumference during 6 months evaluated by an anthropometric tape following the ISAK protocol.
Time Frame: Change from baseline in waist and hip circumference at 6 months
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The waist and hip circumference are measured following the ISAK protocol and measurement technique with an anthropometric tape (Holtain).
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Change from baseline in waist and hip circumference at 6 months
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Change in height jump during 6 months evaluated by countermovement jump test
Time Frame: Change from baseline in countermovement jump at 6 months
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Jump is measured by calculating flight height during countermoving jumps (CMJ) with a Kistler force platform.
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Change from baseline in countermovement jump at 6 months
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Change in maximum manual pressure during 6 months evaluated by a manual dynamometry.
Time Frame: Change from baseline in dynamometry at 6 months
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Maximum manual pressure force measured by a manual dynamometry is performed with a Takei-Grip dynamometer (Espana-Romero, 2010) from 5 to 100 kg adjusting the grip to the optimal measure to develop the greatest strength as described for boys and girls
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Change from baseline in dynamometry at 6 months
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Change in knee extension isometric strength during 6 months evaluated by a strain gage.
Time Frame: Change from baseline in isometric knee extension strength at 6 months
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The isometric maximum force of quadriceps extension is evaluated by means of a strain gage anchored firmly to the wall and connected to a specific interface (MuscleLab); the force exerted by the subject for 10 seconds is measured and the maximum peak force is recorded.
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Change from baseline in isometric knee extension strength at 6 months
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Change in cardiorespiratory fitness during 6 months evaluated by a continuous progressive stress test
Time Frame: Change from baseline in cardiorespiratory fitness at 6 months
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To assess cardiorespiratory resistance, a continuous progressive test will be carried out until exhaustion, with electrocardiographic control and breath-by-breath gas analysis to measure VO2max by a maximum test with gas analyzer (Oxycon Pro, Jaeger / Viasys, Germany).
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Change from baseline in cardiorespiratory fitness at 6 months
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Change in the level of physical activity during 6 months evaluated by accelerometry.
Time Frame: Change from baseline in physical activity at 6 months
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Accelerometer measures diferent intensities of physical activity during 1 week before and after the training with videogames
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Change from baseline in physical activity at 6 months
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Change in markers of inflammation and metabolic risk during 6 months evaluated by blood analysis
Time Frame: Change from baseline in markers of inflammation at 6 months
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to evaluated the biochemical analysis
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Change from baseline in markers of inflammation at 6 months
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Change in systolic blood pressure during 6 months evaluated by sphygmomanometer
Time Frame: Change from baseline in systolic blood preasure at 6 months
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Systolic blood pressure are measured, in duplicate, at rest with a sphygmomanometer (Omron M3).
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Change from baseline in systolic blood preasure at 6 months
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Change in diastolic blood pressure during 6 months evaluated by sphygmomanometer.
Time Frame: Change from baseline in diastolic blood pressure at 6 months
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Diastolic blood pressure are measured, in duplicate, at rest with a sphygmomanometer (Omron M3).
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Change from baseline in diastolic blood pressure at 6 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in nutrition habits during 6 months evaluated by a questionnaire
Time Frame: Change from baseline in nutrition habits at 6 months
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A questionnaire are used, to evaluated the nutritional habits
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Change from baseline in nutrition habits at 6 months
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Change in pubertal development during 6 months evaluated by Tanner stages.
Time Frame: Change from baseline in pubertal development at 6 months
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An experienced physician directly evaluates pubertal development by participants' Tanner stages.
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Change from baseline in pubertal development at 6 months
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Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- DEP2017-85194-P
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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