Descriptive Pilot Study of the Effects of a Standardized Neuromodulation Program on Cortical Brain Function in Chronic Low Back Pain Patients

Inclusion Criteria:

• Patient with a wifi connexion at home

• Patient with the ability to modulate the height of the candle by thinking in thealpha synchrony test.

• Patient with chronic low back pain for more than six months with a visual analoguepain scale greater than 5 impacting activities of daily living, hobbies and work

• Patient having given free and informed consent and signed consent.

• Affected patient or beneficiary of a health insurance plan.

• Patient who is at least 18 years old (≥) and younger than 75 years old (<).

Exclusion Criteria:

• Pregnant or breastfeeding patient

• Patient with a contraindication to performing a fMRI scan: ferromagnetic implant inthe body, piercing, claustrophobia, unable to remain in the scanner stationary for 40 minutes

• Patient already included in another study

• Patient in a exclusion period determined by a previous study

• The subject is under the protection of justice, guardianship or curatorship.

• The subject refuses to sign the consent.

• It is not possible to give the subject informed information.