Informations générales (source: ClinicalTrials.gov)
Neuromodulation by Non-invasive Brain Stimulation (NEUROMOD) (NEUROMOD)
Interventional
N/A
University Hospital, Grenoble (Voir sur ClinicalTrials)
août 2017
juin 2020
29 juin 2024
The main objective of this study is to estimate the effect of the neuromodulation on the
behavioral performances during the access in semantics according to the age of the
individuals.
Neuromodulation by non-invasive stimulation allows to explore the functioning of the
brain by exciting or by inhibiting localized cortical zones. The modulation of the
performances in cognitive tasks, further to the neuromodulation of these zones, allows to
deduce on their functional roles.
Etablissements
| Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
|---|---|---|---|---|---|
| CHU - 38043 - Grenoble - France | Thierry BOUGEROL | Contact (sur clinicalTrials) | |||
Critères
Tous
Inclusion Criteria:
- Major healthy Subject ( 18 - 85 years)
- Right-hander
- Signed Informed consent
- A medical examination must be made before the participation for the research
- Membership in or beneficiary of a national insurance scheme
Non inclusion Criteria:
- Subject under age 18 and of more than 85 years.
- Contraindications in the practice of MRI, TMS and tES
- Existence of a severe affection on the general plan: cardiac, respiratory,
hematological, renal, hepatic, cancerous
- Regular taking of anxiolytic, sedative, antidepressant, neuroleptic
- Characterized psychiatric pathology
- Ingestion of alcohol before the examination
- Pregnancy, parturiency or breast-feeding
- Private person of freedom by court or administrative order, nobody being the object
of a legal protective measure (under guardianship or guardianship)
- Participation to other protocols of current search with period of exclusion or in
the previous week
- Subject which would perceive more than 4500 euros of compensation because of its
participation in other searches involving the human person in 12 months preceding
this study.
- Major healthy Subject ( 18 - 85 years)
- Right-hander
- Signed Informed consent
- A medical examination must be made before the participation for the research
- Membership in or beneficiary of a national insurance scheme
Non inclusion Criteria:
- Subject under age 18 and of more than 85 years.
- Contraindications in the practice of MRI, TMS and tES
- Existence of a severe affection on the general plan: cardiac, respiratory,
hematological, renal, hepatic, cancerous
- Regular taking of anxiolytic, sedative, antidepressant, neuroleptic
- Characterized psychiatric pathology
- Ingestion of alcohol before the examination
- Pregnancy, parturiency or breast-feeding
- Private person of freedom by court or administrative order, nobody being the object
of a legal protective measure (under guardianship or guardianship)
- Participation to other protocols of current search with period of exclusion or in
the previous week
- Subject which would perceive more than 4500 euros of compensation because of its
participation in other searches involving the human person in 12 months preceding
this study.