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Brain stimulation for depression-associated symptoms – a real-world clinical investigation of noninvasive brain stimulation treatments offered at the Department of Psychiatry and Psychotherapy of the LMU Hospital

Brain stimulation for depression-associated symptoms – a real-world clinical investigation of noninvasive brain stimulation treatments offered at the Department of Psychiatry and Psychotherapy of the LMU Hospital

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00024776
Enrollment
1300
Registered
2022-04-28
Start date
2021-05-29
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

other: depressive symptoms of bipolar disorder, negative symptoms of schizophrenia Healthy volunteers F32

Interventions

Group 1: Patients undergoing NTBS treatment (TMS, tDCS) at our department will be assessed with structured questionnaires, including e.g. the MADRS and BDI questionnaires, and neuroimaging Group 2: He

Sponsors

Department of Psychiatry and Psychotherapy, LMU Hospital Munich
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: - Indication for NTBS treatment for a depressive episode as assessed by the clinical evaluation - Patient preference for NTBS treatment - Capable and willing to provide informed consent.

Exclusion criteria

Exclusion criteria: - Individuals with a substance abuse disorder or substance dependence (except nicotine, caffeine) in the last 6 months - Individuals at suicidal risk - Any relevant instable medical condition (e.g. acute, unstable cardiac disease) - Individuals diagnosed with a significant neurological disorder or insult including, but not limited to: o Increased intracranial pressure o Space occupying brain lesion o History of cerebrovascular accident o Transient ischemic attack within two years o Cerebral aneurysm o Huntington’s chorea o Multiple sclerosis o Epilepsy - Individuals with a history of severe traumatic brain injury or status post brain/heart surgery - In general, individuals with any history of seizures - Individuals with significant anatomical abnormalities as seen on cerebral MRI - Individuals with non-removable, ferromagnetic implants/material in proximity to application site (e.g. cochlear implant, implanted neurostimulators, nails, clips, etc.) or treatment-relevant ferromagnetic implants in other body parts (e.g. cardiac pacemaker) - For tDCS specifically – severe skin disorders (e.g. psoriasis vulgaris) in proximity to application site

Design outcomes

Primary

MeasureTime frame
Depression severity assessed by MADRS at the end of (acute) treatment

Secondary

MeasureTime frame
BDI, HDRS, other clinical scales, cognitive performance, neuroimaging parameters

Countries

Germany

Contacts

Public ContactLucia Bulubas

Department of Psychiatry and Psychotherapy, LMU Hospital Munich

lucia.bulubas@med.uni-muenchen.de089-4400-55821

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026