Healthy adults
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Subjects with no history of psychiatric disorders or head injury 2) Subjects not taking drugs affecting cognitive functions 3) Subjects who have the ability to provide informed consent by their free will
Exclusion criteria
Exclusion criteria: 1) Pregnant woman, woman suspected of being pregnant 2) Subjects with history of migraine, seizure disorders, epilepsy 3) Subjects with scalp problems 4) Subjects who have metal implants such as a heart pacemaker 5) Subjects with history of adverse effects to tDCS or other brain stimulation techniques 6) Smokers 7) Subjects taking caffeine 2 days before or alcohol the day before the trial 8) Subjects who are judged as not suitable for participation in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Signal changes in fMRI (BOLD signal) after stimulation | — |
Countries
Japan
Contacts
Nippon Medical School Department of Pharmacology