Active Videogames Against Obesity in Children (VIDEOACTIVO)

January 11, 2024 updated by: José A. Casajús, Universidad de Zaragoza

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:

  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
  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 Overview

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

Interventional

Enrollment (Actual)

92

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Zaragoza, Spain, 50009
        • José Antonio Casajús Mallén

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

9 years to 11 years (Child)

Accepts Healthy Volunteers

Yes

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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.
An intervention with active video-games to increase physical activity and improve body composition
No Intervention: control group
no physical intevention will be provided, but it will be included some sessions on nutritional advice.

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
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).
Change from baseline in fat mass at 6 months
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
Height is measured with a height rod to the nearest 0.1 cm (SECA 225, SECA, Hamburg, Germany),
Change from baseline in size at 6 months
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
Weight of the children is measured by a 0.1 kg precision bascule (SECA 861, SECA, Hamburg, Germany)
Change from baseline in weight at 6 months
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
The waist and hip circumference are measured following the ISAK protocol and measurement technique with an anthropometric tape (Holtain).
Change from baseline in waist and hip circumference at 6 months
Change in height jump during 6 months evaluated by countermovement jump test
Time Frame: Change from baseline in countermovement jump at 6 months
Jump is measured by calculating flight height during countermoving jumps (CMJ) with a Kistler force platform.
Change from baseline in countermovement jump at 6 months
Change in maximum manual pressure during 6 months evaluated by a manual dynamometry.
Time Frame: Change from baseline in dynamometry at 6 months
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
Change from baseline in dynamometry at 6 months
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
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.
Change from baseline in isometric knee extension strength at 6 months
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
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).
Change from baseline in cardiorespiratory fitness at 6 months
Change in the level of physical activity during 6 months evaluated by accelerometry.
Time Frame: Change from baseline in physical activity at 6 months
Accelerometer measures diferent intensities of physical activity during 1 week before and after the training with videogames
Change from baseline in physical activity at 6 months
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
to evaluated the biochemical analysis
Change from baseline in markers of inflammation at 6 months
Change in systolic blood pressure during 6 months evaluated by sphygmomanometer
Time Frame: Change from baseline in systolic blood preasure at 6 months
Systolic blood pressure are measured, in duplicate, at rest with a sphygmomanometer (Omron M3).
Change from baseline in systolic blood preasure at 6 months
Change in diastolic blood pressure during 6 months evaluated by sphygmomanometer.
Time Frame: Change from baseline in diastolic blood pressure at 6 months
Diastolic blood pressure are measured, in duplicate, at rest with a sphygmomanometer (Omron M3).
Change from baseline in diastolic blood pressure at 6 months

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
A questionnaire are used, to evaluated the nutritional habits
Change from baseline in nutrition habits at 6 months
Change in pubertal development during 6 months evaluated by Tanner stages.
Time Frame: Change from baseline in pubertal development at 6 months
An experienced physician directly evaluates pubertal development by participants' Tanner stages.
Change from baseline in pubertal development at 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 5, 2018

Primary Completion (Actual)

June 30, 2021

Study Completion (Actual)

December 31, 2021

Study Registration Dates

First Submitted

March 13, 2019

First Submitted That Met QC Criteria

June 4, 2020

First Posted (Actual)

June 5, 2020

Study Record Updates

Last Update Posted (Actual)

January 12, 2024

Last Update Submitted That Met QC Criteria

January 11, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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