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Maintenance repetitive transcranial magnetic stimulation (rTMS) for treatment-resistant depression

Maintenance repetitive transcranial magnetic stimulation (rTMS) for treatment-resistant depression: a multisite, prospective, non-randomized longitudinal study - mTMS-D

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1032220048
Enrollment
200
Registered
2022-05-01
Start date
2022-10-20
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

Depression Depression

Interventions

After acute rTMS therapy, maintenance rTMS therapy will be administered for 12 months: once a week for the first 6 months and once every two weeks for the latter 6 months.
Transcranial magnetic stimulation

Sponsors

Hayashi Daisuke
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Those who: 1) are aged >=18 and have responded or remitted by acute repetitive transcranial magnetic stimulation (rTMS) therapy conducted in accordance with the guidelines for the proper use of rTMS 2) are willing to adhere to the treatment schedule if the patients wish to receive maintenance rTMS therapy

Exclusion criteria

Exclusion criteria: Those who: 1) are in pregnancy 2) have significant suicidal ideation (HAMD17 suicide item score of 3 or higher) 3) experienced serious adverse events during acute rTMS therapy 4) are deemded inappropriate to participate by judgement of principal investigator

Design outcomes

Primary

MeasureTime frame
Rates of relapse/recurrence up to 12 months after enrollment

Secondary

MeasureTime frame
1) relapse/recurrence rates at 3, 6, and 9 months after enrollment (subjects who relapsed/recurred prior to each assessment period will be treated as relapsing /recurring thereafter.) 2) response rates at 3, 6, 9, and 12 months after enrollment 3) remission rates at 3, 6, 9, and 12 months after enrollment 4) change in the scores of HAMD17, MADRS, QIDS, and PHQ-9 after enrollment 5) period from enrollment until relapse /recurrence 6) adverse events 7) malfunction

Contacts

Public ContactNemoto Kazuki

Satt Co., Ltd

mtmsd@sa-tt.co.jp+81-3-5312-5026

Outcome results

None listed

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