Skip to content

Exergaming to Increase Physical Activity in Overweight/Obese Children and Adolescents

Exergaming to Increase Physical Activity in Overweight/Obese Children and Adolescents

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04122950
Enrollment
6
Registered
2019-10-10
Start date
2020-02-24
Completion date
2022-03-28
Last updated
2022-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

Exercise therapy, Physical fitness, Gaming, Child, Healthy lifestyle, Fitness testing

Brief summary

The primary purpose of this study is to examine the effects of regular exergaming for 8 weeks in 24 overweight/obese children and adolescents (10-17 years) on maximal aerobic fitness (VO2max) and physical activity levels measured before and after (8 weeks) intervention period, and in addition at follow-up (12 weeks). We also wish to investigate the effects on markers of cardio metabolic health and body composition, measured at baseline, 8 weeks and 12 weeks follow-up. Also, the participants gaming frequency will be registered throughout the 8 week period, as well as during the follow-up between 8 and 12 weeks. Aim of this study is to investigate if access to this game can provide health benefits for overweight/obese children and adolescents.

Interventions

BEHAVIORALExergaming

The participants in the Exergaming group will use the PlayPulse exergame for 45 minutes a minimum of three times per week for 8 weeks. Between 8 and 12 weeks the exergaming group will be provided with free access to the exergame but without the two mandatory exergaming sessions

Sponsors

Norwegian University of Science and Technology
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
10 Years to 24 Years
Healthy volunteers
No

Inclusion criteria

* Defined as overweight/obese for age and sex * Able to ride a bike for up to 60 minutes

Exclusion criteria

* Known cardiovascular disease * Taking beta-blockers or anti-arrhythmic drugs * Other diseases that restrict them from doing High-Intensity Training

Design outcomes

Primary

MeasureTime frameDescription
Daily time physical activity (moderate, vigorous and very vigorous)12 weeksMeasured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period and at 12 weeks.

Secondary

MeasureTime frameDescription
Daily average number of steps8 and 12 weeksMeasured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 8 weeks and 12 weeks.
Daily time in sedentary activity (< 3.0 metabolic equivalents = METs)8 and 12 weeksMeasured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 8 weeks and 12 weeks.
Daily time in moderate intensity activity (3.0-6.0 metabolic equivalents = METs)8 and 12 weeksMeasured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 8 weeks and 12 weeks.
Daily time in vigorous intensity activity8 and 12 weeksMeasured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 8 weeks and 12 weeks.
Daily time in very vigorous intensity activity (>9.0 metabolic equivalents = METs)8 and 12 weeksMeasured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 8 weeks and 12 weeks.
Daily average total physical activity duration8 and 12 weeksMeasured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 8 weeks and 12 weeks.
Bioelectrical impedance8 and 12 weeksBody composition assessed using bioelectrical impedance analysis (InBody 720)
Daily average energy expenditure8 and 12 weeksMeasured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 8 weeks and 12 weeks.
Fasting circulating glucose, as blood marker of cardiometabolic health8 and 12 weeks
Fasting triglycerides, LDL-, HDL- and Total cholesterol, as blood marker of cardiometabolic health8 and 12 weeks
Circulating insulin concentration, as blood marker of cardiometabolic health8 and 12 weeks
glucose response to a 2 hour glucose tolerance test, as blood marker of cardiometabolic health8 and 12 weeks
VO2max8 and 12 weeksMaximal Aerobic Capacity
Daily time physical activity (moderate, vigorous and very vigorous)8 weeksMeasured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period and at 8 weeks
Blood Pressure8 and 12 weeks

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026