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A multisite observational study on the effectiveness of repetitive transcranial magnetic stimulation therapy for patients with treatment-resistant depression under health insurance coverage in Japan

A multisite observational study on the effectiveness of repetitive transcranial magnetic stimulation therapy for patients with treatment-resistant depression under health insurance coverage in Japan - Multisite real-world rTMS study for TRD in Japan

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000054747
Enrollment
500
Registered
2024-08-01
Start date
2024-08-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Major depressive disorder

Interventions

None listed

Sponsors

Fujita Health University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adult patients diagnosed with major depressive disorder according to DSM-5 criteria by a psychiatrist Patients with moderate to severe depressive symptoms who have not responded to adequate doses and duration of antidepressant therapy during the current episode

Exclusion criteria

Exclusion criteria: Patients with psychotic features, bipolar disorder, mild depressive episodes, persistent depression Patients with active suicidal ideation Patients with ferromagnetic implants in the upper body (cardiac pacemakers, cochlear implants, ferromagnetic intracranial aneurysm clips, and deep brain stimulation) Patients who have received rTMS therapy in the current episode Patients with residual affective disorders due to psychoactive substance use and polypharmacy Patients with a diagnosis of dementia, organic or symptomatic psychiatric disorder.

Design outcomes

Primary

MeasureTime frame
Change in HAMD-17 score from baseline to endpoint

Secondary

MeasureTime frame
Change in MADRS score from baseline to endpoint Change in PHQ-9 score from baseline to endpoint Response rate and remission rate at 3 and 6 weeks

Countries

Japan

Contacts

Public ContactYuki Matsuda

Fujita Health University Department of Development and Education of Clinical Research

myuki@fujita-hu.ac.jp0562-93-2000

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026