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The Dose-Effect of Acute Exergaming on Inhibitory Control in Sedentary University Students

Dose-Response Effects of Acute Exergaming on Inhibitory Control in Sedentary University Students: An fNIRS Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114475
Enrollment
Unknown
Registered
2025-12-12
Start date
2025-12-13
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

Inhibitory control

Interventions

Sequence 1 (Order Group 1): A (moderate-intensity, high cognitive engagement) ? B (moderate-intensity, low cognitive engagement) ? D (low-intensity, low cognitive engagement) ? C (low-intensity, high
Sequence 2 (Order Group 2): B (moderate-intensity, low cognitive engagement) ? C (low-intensity, high cognitive engagement) ? A (moderate-intensity, high cognitive engagement) ? D (low-intensity, low
Sequence 3 (Order Group 3): C (low-intensity, high cognitive engagement) ? D (low-intensity, low cognitive engagement) ? B (moderate-intensity, low cognitive engagement) ? A (moderate-intensity, high
Seq

Sponsors

Shenyang Sport University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Health Status: Self-reported good health, without a history of head trauma or neurological disorders (e.g., concussion, epilepsy, stroke); 2.Visual Function: Normal color discrimination ability, capable of accurately distinguishing red, green, and blue colors, and able to successfully complete the Stroop task; 3.Emotional State: Self-reported absence of clinically diagnosed anxiety, depression, or other mood disorders that severely affect cognitive function; 4.Sedentary Behavior: Assessed using the Chinese version of the Adults Sedentary Behavior Questionnaire, average daily recreational screen-based sedentary time (including non-purposeful web browsing, passive video watching) in the past week exceeded 3 hours; 5.Informed Consent: Ability to understand the study procedures, voluntary participation, and provision of written informed consent.

Exclusion criteria

Exclusion criteria: 1.History of Neurological or Psychiatric Disorders: A clear diagnosis of neurological diseases, psychiatric disorders, or history of severe head trauma; 2.Color Vision Deficiency: Presence of color blindness or color weakness, confirmed by standard color vision test charts; 3.Mood Disorders: Clinical diagnosis of anxiety, depression, or other mood disorders, or current use of related psychotropic medications; 4.Physical Activity Level: Being a high-level athlete or regularly engaging in high-intensity physical activity (assessed by the International Physical Activity Questionnaire as falling into the highly active category), thus not meeting the core characteristic of being "sedentary"; 5.Contraindications to Exercise: Presence of musculoskeletal, cardiovascular, or other systemic diseases that prevent safe completion of the moderate-intensity exergaming intervention.

Design outcomes

Primary

MeasureTime frame
Reaction time of the Stroop task conflict effect;Reaction time and accuracy of the Go/Nogo task;Changes in oxygenated hemoglobin concentration (HbO-ß) in the prefrontal and motor-related brain regions;

Countries

China

Contacts

Public ContactZhao Hongpeng

Shenyang Sport University

Clark-72@163.com+86 138 9796 6507

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026