Institute of Biomedical engineering,Chinese Academy of Medical Sciences & Peking Union Medical College
Tianjin, Tianjin Municipality, 300000, China
NCT Number: NCT07018817
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.
Looking for future studies?
Notify MeAll sexes
Observational
Tianjin, Tianjin Municipality, 300000, China
This study employed a multimodal acquisition system comprising EEG, EMG, and fNIRS modules. Participants were fitted with a 64-channel dry EEG cap for the measurement of cortical electrical activity. Surface EMG electrodes were attached to three muscle groups: the right biceps brachii, the flexor digitorum profundus of the forearm, and the gastrocnemius muscle, to record muscle activation signals. Simultaneously, fNIRS probes were positioned on the participants' foreheads to monitor cerebral hemodynamic responses.
The experimental paradigm was divided into two tasks: motor execution (ME) and motor imagery (MI). During the ME task, participants performed 15 trials of actual movements, whereas the MI task involved 60 trials of imagined movements. Each trial randomly presented one of three stimuli-left-hand clenching, right-hand clenching, or bilateral heel raising-with an equal distribution of the three movement types across the session. The order of stimuli was randomized to prevent prediction bias.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will perform motor execution tasks and motor imagery tasks following standardized instructions under controlled conditions.
Time frame: up to 2 weeks
Time frame: up to 2 weeks
Time frame: up to 2 weeks
Peking Union Medical College
Other
A Trimodal Study on Hypoxia Adaptation: Promotion of Cerebral Functional Connectivity and Decrement of Neuromuscular Efficiency
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04075565
Altitude, Altitude Hypoxia
Landquart, Kanton Graubünden, Switzerland
View Trial DetailsNCT05588427
Acid-Base Imbalance, Acidosis
Leuven, Vlaams-Brabant, Belgium
View Trial DetailsNCT00731510
Altitude Sickness, Hypoxia
Pinfold, Hyssington, Montgomery, Powys, United Kingdom
View Trial DetailsNCT00498563
Altitude, Altitude Sickness
Tulsa, Oklahoma, United States
View Trial Details