Our objective is to study the AEs produced by tDCS and its temporal evolution in a closer context to the clinical application, during 5 days of application
We have recorded the adverse effects scored by healthy and young volunteers that recieved tDCS or sham stimulation (randomized). Simulating clinical conditions, participants performed a hand dexterity task meanwhile received the intervention (20 minutes and 1 mA), during 5 consecutive days. AEs were assessed after each intervention and classified in somatosensory, pain or other effects, to facility the analysis (Clinical Trial number: NCT03931512).