NCT07018817

Brief Summary

The study utilized a trimodal setup comprising EEG, EMG, and fNIRS modules. Participants wore a 64-channel dry EEG cap, while EMG electrodes were placed on the right biceps brachii, the flexor digitorum profundus of the forearm, and the gastrocnemius muscle. fNIRS probes were positioned on the forehead to monitor cerebral hemodynamic responses. The experimental paradigm included two tasks: motor execution (ME) and motor imagery (MI). During ME, participants performed 15 trials of actual movements. In MI, participants completed 60 trials of imagined movements. Each trial involved a randomly presented stimulus-left-hand clenching, right-hand clenching, or bilateral heel raising-with each movement type occurring an equal number of times across the session.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jul 2023

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 15, 2023

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 23, 2024

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 15, 2024

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

April 27, 2025

Completed
2 months until next milestone

First Posted

Study publicly available on registry

June 13, 2025

Completed
Last Updated

June 13, 2025

Status Verified

April 1, 2025

Enrollment Period

1.1 years

First QC Date

April 27, 2025

Last Update Submit

June 4, 2025

Conditions

Keywords

Brain

Outcome Measures

Primary Outcomes (1)

  • EEG Power Spectrum in Motor Imagery and Motor Execution Tasks

    up to 2 weeks

Secondary Outcomes (2)

  • Surface EMG Amplitude of Upper Limb Muscles during Motor Tasks

    up to 2 weeks

  • Cerebral Oxygenation Measured by Near-Infrared Spectroscopy (NIRS) in Prefrontal Cortex

    up to 2 weeks

Interventions

Participants will perform motor execution tasks and motor imagery tasks following standardized instructions under controlled conditions.

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Short-term migration from the highlands

You may qualify if:

  • People who can withstand altitude sickness

You may not qualify if:

  • Plateau Native

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Institute of Biomedical engineering,Chinese Academy of Medical Sciences & Peking Union Medical College

Tianjin, Tianjin Municipality, 300000, China

Location

Related Links

MeSH Terms

Conditions

HypoxiaAltitude Sickness

Condition Hierarchy (Ancestors)

Signs and Symptoms, RespiratorySigns and SymptomsPathological Conditions, Signs and SymptomsRespiration DisordersRespiratory Tract Diseases

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Full professor

Study Record Dates

First Submitted

April 27, 2025

First Posted

June 13, 2025

Study Start

July 15, 2023

Primary Completion

August 23, 2024

Study Completion

December 15, 2024

Last Updated

June 13, 2025

Record last verified: 2025-04

Locations