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Gaming and Training Combined to Help Adolescents Get More Physically Active

Increasing Physical Activity Among Adolescents With Motivational High-Intensity Training Through a Cutting-Edge Gaming Platform

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03663699
Enrollment
29
Registered
2018-09-10
Start date
2019-02-11
Completion date
2021-04-07
Last updated
2021-04-23

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

Conditions

Sedentary Lifestyle

Keywords

Exercise Therapy, Physical Fitness, Games, Recreational, Children, Adolescents, Healthy Lifestyle, Exercise Test

Brief summary

The purpose of this study is to investigate if playing a newly developed videogame that requires physical activity (e.g. exergame), leads to increased physical activity and health benefits in children and adolescents who do not regularly participate in endurance training. Health benefits will be expressed in physical fitness (maximal oxygen consumption), blood markers of a healthy heart, body composition and objectively measured physical activity. Gaming frequency of the participants will be registered throughout the 24 week intervention period.

Interventions

BEHAVIORALExergaming

free access to the exergaming platform PlayPulse for 24 weeks

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
12 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Not regularly participating in endurance training * Sedentary (\<60 mins daily moderate/vigorous intensity physical activity) * Play video games \> 10 hours/week (self-reported) * Able to ride a bike for up to 60 minutes

Exclusion criteria

* Known cardiovascular disease * Type I diabetes

Design outcomes

Primary

MeasureTime frameDescription
VO2max12 weeksMaximal Aerobic Capacity

Secondary

MeasureTime frameDescription
Change in daily time in sedentary activity (<3.0 metabolic equivalents =METs)Baseline, 12 and 24 weeksMeasured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 12 weeks and 24 weeks.
Change in daily time in moderate intensity activity (3.0-6.0 metabolic equivalents = METs)Baseline, 12 and 24 weeksMeasured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 12 weeks and 24 weeks.
Change in daily time in vigorous intensity activity (6.0-9.0 metabolic equivalents = METs)Baseline, 12 and 24 weeksMeasured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 12 weeks and 24 weeks.
Change in daily time in very vigorous intensity activity (>9.0 metabolic equivalents = METs)Baseline, 12 and 24 weeksMeasured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 12 weeks and 24 weeks.
Change in daily average total physical activity durationBaseline, 12 and 24 weeksMeasured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 12 weeks and 24 weeks.
Change in daily average number of stepsBaseline, 12 and 24 weeksMeasured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 12 weeks and 24 weeks.
Change in daily average energy expenditureBaseline, 12 and 24 weeksMeasured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 12 weeks and 24 weeks.
systolic Blood Pressure12 and 24 weeks
Diastolic Blood Pressure12 and 24 weeks
Fasting circulating glucose, as blood marker of cardiometabolic health24 weeks
Lipid profile, as blood marker of cardiometabolic health24 weeks
Circulating insulin concentration, as blood marker of cardiometabolic health24 weeks
HbA1c from blood samples24 weeks
Bioelectrical impedance12 and 24 weeksBody composition assessed using bioelectrical impedance analysis (InBody 720)

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 10, 2026