Neuromodulation by Non-invasive Brain Stimulation (NEUROMOD)

Grenoble Alpes University Hospital Center (CHU)

Status: Unknown

Conditions: Healthy; Transcranial Direct Current Stimulation; Transcranial Magnetic Stimulation

Treatments: Other: transcranial electric stimulation + electroencephalogram; Other: MRI + transcranial Magnetic Stimulation

Study type: Interventional

Funder types: Other

Identifiers

NCT03167931

2017-A00834-49 (Other Identifier)

38RC17.078

Details and patient eligibility

About

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.

Full description

The objective of this project is to determine the changes of behavioral performances (time of answer, percentage of correct answers) further to the neuromodulation. The specific question is to estimate the effect on the performances of access at the semantic representations of this method, according to the age. One of the hypotheses in the research on the normal ageing is the difficulty of access to these representations (fundamental process for the cognitive functions, such as the language and the memory) at the healthy elderly. By using the neuromodulation the investigators wish to explore this hypothesis and to understand if the neuromodulation can have a beneficial effect on the improvement of the behavioral performances of the elderly.

Enrollment: 120 estimated patients

Sex: All

Ages: 18 to 85 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

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.

Trial design

Primary purpose: Basic Science

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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120 participants in 2 patient groups

18-49 years group

Experimental group

Description:

Participants undergo 2 sessions of MRI + transcranial Magnetic Stimulation or transcranial electric stimulation + electroencephalogram. The 2 sessions are performed with an interval of 3 to 7 days.

Treatment:

Other: transcranial electric stimulation + electroencephalogram

Other: MRI + transcranial Magnetic Stimulation

50-85 years group

Experimental group

Description:

Participants undergo 2 sessions of MRI + transcranial Magnetic Stimulation or transcranial electric stimulation + electroencephalogram. The 2 sessions are performed with an interval of 3 to 7 days.

Treatment:

Other: transcranial electric stimulation + electroencephalogram

Other: MRI + transcranial Magnetic Stimulation