Intermittent Theta Burst Stimulation of the Precuneus

Other illness

• Patient with a contraindication to magnetic resonance imaging or intermittent Theta Burst Stimulation (presence of a metallic body, pacemaker, implantable defibrillator or other implantable metallic device, epilepsy, stroke or recent head trauma);
• Patient in forced care (psychiatric care upon decision of the State representative and psychiatric care at the request of a third party);

Age

• Pregnant woman or likely to be pregnant (of childbearing age) without effective contraception or breastfeeding;

Other

• Patient who is not French-speaking or cannot read and write;
• Patient under guardianship;
• Patient participating in another clinical trial, or during a period of exclusion from another clinical trial;
• Patient who is not a beneficiary of a social security system.
• Patient who, according to the assessment of the investigator, risks not being compliant or diligent in the study procedures.

• Right-handed patient aged 18 to 40 years inclusive;
• Patient presenting schizophrenia as defined in the Diagnostic and Statistical Manual-5;
• Patient under antipsychotic treatment in accordance with the recommendations of the High Authority of Health, at a stable dosage and without modification of psychotherapeutic treatment for at least 4 weeks;
• Patient on mono or dual antipsychotic therapy.
• Patient presenting residual symptoms, i.e. absence of remission defined by the criteria of the "Remission criteria of the Schizophrenia Working Group Consensus";
• Patient having been exposed to at least one type of trauma in childhood and having a score higher than the threshold values of the childhood trauma questionnaire: emotional neglect, physical abuse, emotional abuse, physical neglect, sexual abuse;
• Patient having signed an informed consent form to participate in the study.