CClinicalTrials.gg
CompletedNCT03513380Updated Dec 11, 2019

Can Gaming Get You Fit? A High-Intensity Exergaming Intervention in Adults

An interventional study of Exergaming in Sedentary Lifestyle, sponsored by Norwegian University of Science and Technology. Completed at 1 site in Norway. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-12-11.

Sponsored by Norwegian University of Science and Technology · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
52
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this project is to assess if playing a newly developed videogame that require physical activity (e.g. exergame) can lead to health benefits. The project will include 50 adult participants that are not particularly physically active. They will be randomized into two groups where one group will be given free access to the exergame for 6 months. The physical fitness (maximal oxygen consumption), blood markers of cardiometabolic health and body composition of the subjects will be tested before, mid-ways and after the intervention period. Also, the participants gaming frequency will be registered throughout the 6-month period. Aim of this study is to investigate if access to this game can provide health benefits for individuals who are not motivated to take part in regular physical activity.

02

Conditions studied

  • Sedentary Lifestyle

Keywords

  • Exercise therapy
  • Physical fitness
  • Gaming
  • Adult
  • Healthy lifestyle
  • Fitness testing
03

In context

Lead sponsor

Norwegian University of Science and Technology is the lead sponsor of 487 studies on the registry; 52 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Sedentary (\<150 mins of moderate intensity physical activity/week)
  • Able to ride a bike for up to 60 minutes

Exclusion criteria

Exclusion Criteria:

  • Known cardiovascular disease
  • Taking beta-blockers or anti-arrhythmic drugs
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
52 participants (actual)

Study arms

  • Experimental
    Exergaming

    free access to the exergame PedalTanks

    Behavioral: Exergaming

  • No intervention
    Control

    recommended to continue with their normal daily routine

Interventions

  • BehavioralExergaming

    free access to the exergame PedalTanks during 6 months

    Also known as: PlayPulse, PedalTanks

06

What researchers measure

Primary outcomes

  1. VO2max (Maximal Aerobic Capacity)

    Time frame: 3 months

  2. VO2max (Maximal Aerobic Capacity)

    Time frame: 6 months

Secondary outcomes

  1. Daily average energy expenditure

    Measured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 3-months and 6-months.

    Time frame: 3 and 6 months

  2. Daily average number of steps

    Measured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 3-months and 6-months.

    Time frame: 3 and 6 months

  3. Daily time in sedentary activity (< 3.0 metabolic equivalents = METs)

    Measured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 3-months and 6-months.

    Time frame: 3 and 6 months

  4. Daily time in moderate intensity activity (3.0-6.0 metabolic equivalents = METs)

    Measured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 3-months and 6-months.

    Time frame: 3 and 6 months

  5. Daily time in vigorous intensity activity (6.0-9.0 metabolic equivalents = METs)

    Measured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 3-months and 6-months.

    Time frame: 3 and 6 months

  6. Daily time in very vigorous intensity activity (>9.0 metabolic equivalents = METs)

    Measured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 3-months and 6-months.

    Time frame: 3 and 6 months

  7. Daily average total physical activity duration

    Measured by activity monitors (SenseWear Armband) which participants will wear for one week at start of intervention period, 3-months and 6-months.

    Time frame: 3 and 6 months

  8. Bioelectrical impedance

    Body composition assessed using bioelectrical impedance analysis (InBody 720)

    Time frame: 3 and 6 months

  9. Blood Pressure

    Time frame: 3 and 6 months

  10. Fasting circulating glucose, as blood marker of cardiometabolic health

    Time frame: 6 months

  11. Lipid profile, as blood marker of cardiometabolic health

    Time frame: 6 months

  12. Circulating insulin concentration, as blood marker of cardiometabolic health

    Time frame: 6 months

  13. glucose response to a 2 hour glucose tolerance test, as blood marker of cardiometabolic health

    Time frame: 6 months

07

Study locations

1 site
  • Department of Circulation and Medical Imaging
    Trondheim, 7491, Norway
08

References and documents

Publications

  • Berg J, Wang AI, Lydersen S, Moholdt T. Can Gaming Get You Fit? Front Physiol. 2020 Aug 20;11:1017. doi: 10.3389/fphys.2020.01017. eCollection 2020. PubMed 32973553 ↗

Individual participant data

Plan to share: Undecided

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 11, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03513380
Lead sponsor
Norwegian University of Science and Technology
Responsible party
Sponsor
First posted
May 1, 2018
Start date
May 25, 2018
Primary completion
Nov 30, 2019
Completion
Nov 30, 2019
Last update
Dec 11, 2019

Study contacts

Øystein Risa, PhD
study director · Norwegian University of Science and Technology

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Dec 2019. You cannot join it, but the record below documents what was studied.

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