Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University Medical Center Goettingen
Age
18–60
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Men and women between the ages of 18 and 60 years
Diagnosis of major depressive disorder according to DSM 5 (F32.x according to ICD-10) or bipolar disorder (bipolar I or bipolar II) according to DSM 5 (F31.x according to ICD-10) and an acute depressive condition at the time of the initial examination in outpatient or inpatient treatment (e.g. Department of Psychiatry and Psychotherapy, UMG)
Availability of informed consent to participate in the study, including the examinations and interventions
You may not be if
Neurological diseases, current or previous
Other Axis I diagnoses that mimic the affective disorder, current or previous
Physical illnesses that could be related to the affective symptoms (so-called organic causes)
Illicit drug use in the past month
Substance dependence, current or previous
Physical illnesses which, depending on their type and severity, could interfere with the planned examinations, influence the parameters to be examined or endanger the test participant during the course of the examination
Medical contraindications against performing an MRT examination / rTMS application (such as metal parts in the body, e.g. implants, pacemakers, infusion pumps, metal splinters, etc.)
Pregnancy
Previously known cerebral-morphological abnormalities (e.g. tumor, lesion, etc.)
Evidence or history of epilepsy
Head trauma with a history of loss of consciousness
Unwillingness to be informed of incidental findings
Participation in an rTMS / EKT application within the last 8 weeks
Lack of the ability to provide informed consent
Clareo Health | Pre-mapping Networks for Brain Stimulation 2
