Basic research in healthy participants Healthy participants
Conditions
Interventions
Group 1: The project involves neurophysiological measurements (e.g. fMRI, EEG and EMG) as well as non-invasive brain stimulation (e.g. TMS, tCS) during behavioural tests (e.g. sensorimotor and cogniti
Sponsors
NCM-Lab, ETH Zürich
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Healthy participants Age 18 – 65 years Normal physical and mental health Normal or corrected to normal vision
Exclusion criteria
Exclusion criteria: Known history of neurological, musculoskeletal or neuromuscular disorders. Pregnancy. Participants with metal implants in their body including pacemakers, or electronically/magnetically/mechanically activated implants.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Electrophysiological markers of brain activity as measured with EEG (Electroencephalography). BOLD (blood oxygenation level dependent) signal changes as measured with fMRI (Functional magnetic resonance imaging). Muscle activity as measured with EMG (Electromyography). Performance on behavioural tasks (accuracy, reaction time, and others). Eye and motion tracking measures. The planned end date of the study is 1. September 2024. | — |
Countries
Switzerland
Contacts
Public ContactNicole Wenderoth
NCM-Lab, ETH Zürich
Outcome results
None listed