Effects of EEG- Microstate Neurofeedback on Attention and Impulsivity in Adult Attention-deficit/Hyperactivity Disorder (ADHD) and Neurotypical Controls (ADHDmicroNFB)
ADHD, Healthy
About this trial
This is an interventional basic science trial for ADHD
Eligibility Criteria
ADHD POPULATION GROUP
A subject will be eligible if all the following criteria apply:
- Age: between 18-50 years
- Gender: male and female
- Health: general good health and normal or corrected-to-normal visual acuity
- Patients clinically able to stop the following psychotropic medications for 48h: psychostimulants, benzodiazepines
- Having provided written informed written consent
A subject will not be eligible if any of the following criteria apply:
- Past or current history of a clinically significant central nervous system disorder, including structural brain abnormalities; cerebrovascular disease; history of other neurological disease, epilepsy, stroke or head trauma (defined as loss of consciousness > 5 min or requiring hospitalization)
- Impaired vision (normal or corrected acuity below 20/40)
- Medical illness (e.g., cardiovascular disease, renal failure, hepatic dysfunction)
- Comorbidities with current psychiatric disorders (bipolar disorder, borderline personality disorder, major depressive disorder, anxiety disorder) including substance use disorder as defined by the DIGS.
HEALTHY POPULATION GROUP
A subject will be eligible if all of the following criteria apply:
- Age: between 18-50 years
- Gender: male and female
- Health: general good health and normal or corrected-to-normal visual acuity
- Having provided written informed written consent
A subject will not be eligible if any of the following criteria apply:
- Past or current history of ADHD
- Past or current history of main psychiatric disorders (bipolar disorder, borderline personality disorder, major depressive disorder, anxiety disorder), including substance use disorder as defined by the DIGS.
- Past or current history of a clinically significant central nervous system disorder, including structural brain abnormalities; cerebrovascular disease; history of other neurological disease, including epilepsy, stroke or head trauma (defined as loss of consciousness > 5 min or requiring hospitalization)
- Impaired vision (normal or corrected acuity below 20/40)
- Medical illness (e.g., cardiovascular disease, renal failure, hepatic dysfunction)
Sites / Locations
- TRE Unit (Trouble de la Régulation Emotionnelle) Department of psychiatry, HUGRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
healthy population group
ADHD population group
The experimental design includes three sessions: session 1 will be used to evaluate diagnostic using different targeted questionnaires. sessions 2 and 3 will be decomposed into 3 consecutives parts: Pre evaluation Neurofeedback Post evaluation
The experimental design includes three sessions: session 1 will be used to evaluate diagnostic using different targeted questionnaires. sessions 2 and 3 will be decomposed into 3 consecutives parts: Pre evaluation Neurofeedback Post evaluation