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Not yet recruiting NCT07150312

Can Different Exercise Modalities Improve Esports Performance?

No phase Interventional Esports Players

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: HIIT, MICT.
Who it may be relevant to
Registry conditions: Esports Players. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Can Different Exercise Modalities Improve Esports Performance? Study Protocol for a 12-week Three-arm Randomized Controlled Trial

Overview

This study aims to investigate the long-term effects of high-intensity interval training (HIIT) and moderate-intensity continuous training (MICT) on esports performance through a 12-week three-arm randomized controlled trial, and to examine the sustainability of these effects during a follow-up period after intervention cessation. Additionally, we seek to compare the differential impacts of these two exercise modalities on various dimensions of esports performance, thereby providing evidence-based guidance for esports training regimens and enhancing our understanding of the underlying mechanisms by which different exercise approaches influence cognitive and motor capabilities essential for competitive gaming.

Interventions

  • Behavioral HIIT
    A 12-week home-based HIIT exercise plan (running). Duration: Each session consists of 10 x 1-minute high-intensity bouts interspersed with 10 x 1-minute recovery periods. Adding the 3-minute warmup and 3-minute cool-down, each session totals approximately 26 minutes. This protocol is followed for 12 weeks. Intensity: High-intensity bouts are performed at 80-90% of HRmax (RPE 15-18). Recovery periods are at 40-50% of HRmax (RPE 11-13). Warm-up and cool-down are at 50% HRmax (RPE 11-13). Modalit
  • Behavioral MICT
    A 12-week home-based MICT exercise plan (running). Duration: Each session consists of 20 minutes of continuous exercise. Including the 3-minute warm-up and 3-minute cool-down, each session totals 26 minutes. This protocol is followed for 12 weeks. Intensity: Exercise is performed at 64-76% of HRmax (RPE 12-14). Warm-up and cool-down are at 50% HRmax (RPE 11-13). Modality: Running, jogging, or brisk walking, either on a treadmill or outdoors. Supervision: The first three sessions are supervise

Primary outcome measures

  • Esports performance [Time frame: Baseline (pre-intervention) and immediately after 12-week intervention completion]

Eligibility criteria

Inclusion criteria

  • 18-29 years old;
  • regular FPS players engaging in shooters within the past six months;
  • healthy individuals who are capable of physical tests or HIIT;
  • no regular exercise habits;
  • can understand English or Chinese.

Exclusion criteria

  • self-reported history of neurological, psychiatric, or medical diseases;
  • current intake of medications and/or recreational drugs that could affect the central nervous system and/or the ability to learn;
  • not a regular user of Aim Lab.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Publications

  • DE Las Heras B, Li O, Rodrigues L, Nepveu JF, Roig M. Exercise Improves Video Game Performance: A Win-Win Situation. Med Sci Sports Exerc. 2020 Jul;52(7):1595-1602. doi: 10.1249/MSS.0000000000002277. PMID 31977638

Identifiers

NCT: NCT07150312 · SBRE-24-0942

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗