Healthy Volunteers
Conditions
Interventions
The sample will consist of 68 participants who will be divided into 4 groups in a 1:1:1:1 ratio, as follows: tDCS/2 mA Group (n=17) – which will receive only transcranial stimulation at an intensity o
tDCS/3 mA Group (n=17) – which will receive only transcranial stimulation at an intensity of 3 mA
tDCS/2 mA+binaural Group (n=17) – which will receive transcranial stimulation at an intensity of 2 mA plus binaural frequency
and tDCS/3 mA+binaural Group (n=17) – which will receive transcranial stimulation at an intensity of 3 mA plus binaural frequency. There will be no sham group due to the already proven effectiveness o
E02.331.750
Sponsors
Maria de Cassia Gomes Souza Macedo
Universidade Federal de Juiz de Fora
Eligibility
Age
18 Years to 30 Years
Inclusion criteria
Inclusion criteria: Young adults aged between 18 and 30; with normal hearing; without a history of neuropsychiatric disorders; without the use of psychoactive substances
Exclusion criteria
Exclusion criteria: Participants with metallic materials implanted in or near the head; with pacemakers or cardiac stents; with active devices where interaction with the electrical field may interfere with their operation; individuals with eczema on the head
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected that, through non-invasive neuromodulation protocols, there will be an increase in intracranial SatO2 during and immediately after the application of stimuli, with the best responses anticipated with the combined intervention protocol and at a higher intensity compared to the others | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary stages expected | — |
Countries
Brazil
Contacts
Public ContactMaria Macedo
Universidade Federal de Juiz de Fora
Outcome results
None listed