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Examination of effectiveness on maintenance of continuing treatment and treatment effect in treatment of refractory mood disorder of transcranial direct current stimulation (tDCS)

Examination of effectiveness on maintenance of continuing treatment and treatment effect in treatment of refractory mood disorder of transcranial direct current stimulation (tDCS) - transcranial direct current stimulation open traial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000024953
Enrollment
100
Registered
2017-01-01
Start date
2017-01-01
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

Mood disorder

Interventions

TDCS treatment is performed from once a week to once a month for one year. I plan to stimulate 1-2 mA for 20-30 minutes.

Sponsors

Department of Neuropsychiatry,Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1,Patient in a mood disorder with intractable depressive symptoms during visit to the psychiatry department affiliated hospital of the University of the Ryukyus 2,Age 16 years older, under 65 years old 3,In the past,used more than two kinds of antidepressants (treatment amount on the package insert) and a sufficient period (4 weeks or more) but in Montgomery - Asberg Depression Scale (MADRS) more than 20 4,Persons whose disease duration is one year or more 5,Regarding participation in this research, a person who gained written consent by the patient's free will and consent was obtained by the substitute.

Exclusion criteria

Exclusion criteria: 1,person with a history of head trauma accompanied by consciousness disturbance of 5 minutes or more 2,Persons who have a history of organic diseases in the brain 3,Person who has history of substance dependence or present symptom 4,Persons who have a history of confusion conscious convulsions 5,Persons who have a history of chronic headache 6,Pregnant or potential women

Design outcomes

Primary

MeasureTime frame
Evaluate the remission rate of depression 1 month, 3 months, 6 months, 1 year after treatment start.

Secondary

MeasureTime frame
Remission maintenance rate one year after the start of treatment, each item of neuropsychological examination and various biological indicators, changes in various brain function images

Countries

Japan

Contacts

Public ContactHotaka Shinzato

Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan Department of Neuropsychiatry

hotaka.shinzato@gmail.com098-895-1419

Outcome results

None listed

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