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Differences in executive function at different high altitude conditions between plateau natives and plain settlers: an fNIRS study

Differences in executive function at different high altitude conditions between plateau natives and plain settlers: an fNIRS study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126413
Enrollment
Unknown
Registered
2026-06-09
Start date
2026-06-10
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

Oxygen deficiency

Interventions

2000m-altitude generations living at high altitude:None
Long-term plains residents:None
2000m altitude migrants from the plains:None
3000m altitude migrants from the plains:None
3000m-altitude generations living at high altitude:None

Sponsors

The First Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Age: 18 - 60 years old; 2.There is no history of any diagnosed mental disorders or neurological diseases (such as stroke, epilepsy, dementia, etc.), nor any history of severe head trauma or brain surgery; 3.There are no chronic diseases that may affect cognitive function or cerebral blood flow, such as severe cardiovascular or cerebrovascular diseases, respiratory system diseases, thyroid dysfunction, or hydrocephalus; 4.right handedness; 5.Normal vision and hearing or corrected vision and hearing do not affect the conduct of the experiment; 6.Voluntary participation and signing of the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Pregnant women or women who are breastfeeding; 2.Drugs that may affect cognitive functions or the central nervous system if used for a long time (such as anticholinergic drugs, sedatives, antidepressants, stimulants, etc.); 3.Consumption of alcohol or other psychoactive substances within the last 24 hours; 4.There was insomnia the night before the test. 5.Having participated in other studies involving cognitive tasks or brain function measurements within the past 4 weeks; 6.There are contraindications for fNIRS testing (such as severe skin diseases on the head, allergies to the instrument materials, etc.); 7.Failure to cooperate or lack of seriousness in the cognitive task process; 8.After repeated attempts, one still fails to understand the rules of the cognitive task paradigm.

Design outcomes

Primary

MeasureTime frame
Stop-Signal Paradigm:Go Task Accuracy Rate;Stop-Signal Paradigm: Stop-Signal Failure Rate;Changes in oxyhemoglobin concentration(?HbO);1-back:Criterion;1-back:Reaction Time;1-back:d-prime;1-back:Accuracy;Stop-Signal Paradigm:Go Reaction Time(Go RT);1-back:False Alarm Rate;Stop-Signal Paradigm:Stop-Signal Reaction Time(SSRT);Stop-Signal Paradigm:Stop-Signal Delay(SSD);Deoxyhemoglobin concentration changes(?HHb);1-back:Hit Rate;

Countries

China

Contacts

Public ContactDing Tao

The First Affiliated Hospital of Kunming Medical University

dt101180@sina.com+86 871 65324888

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026