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Repetitive Transcranial Magnetic Stimulation for the Treatment of the Tardive Dyskinesia.

Repetitive Transcranial Magnetic Stimulation for the Treatment of the Tardive Dyskinesia.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02840760
Enrollment
60
Registered
2016-07-21
Start date
2016-09-30
Completion date
2018-12-31
Last updated
2018-02-26

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

Conditions

Tardive Dyskinesia

Keywords

tardive dyskinesia., rTMS

Brief summary

The purpose of this study is to explore the therapeutic effect and mechanism of transcranial magnetic stimulation (rTMS) in the treatment of the tardive dyskinesia.

Detailed description

The study was a parallel control design trial for 2 weeks. Patients with schizophrenia were treated with 10-Hz rTMS on left motor cortex (added to the ongoing treatment). Clinical symptoms and MEP were assessment before and after rTMS treatment.

Interventions

DEVICERepetitive Transcranial Magnetic Stimulation

Stimulate the primary motor cortex for 2 weeks.

Sponsors

Shanghai Mental Health Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* The diagnosis of schizophrenia according to DSM-IV; * At least two item of Abnormal Involuntary Movement Scale(AIMS) must be 2 points or higher * these symptoms are not from Parkinson,tourette's syndrome,huntington disease * Signed an informed consent

Exclusion criteria

* rTMS contraindications: intracranial metal substance, with heart pacemakers and cochlear implants, intracranial pressure * patients to be diagnosed according to DSM-IV for substance abused, development delayed * current treatment with anticonvulsant acting drugs such as anticonvulsants, benzodiazepines * Acute risk of suicide and impulse * history of epileptic seizures or the presence of epileptic activity documented on the basis of EEG * pregnant and lactant women

Design outcomes

Primary

MeasureTime frame
Change from baseline in motor evoked potential(MEP)2 times (Before treatment,immediately after treatment)
Change from baseline in Abnormal Involuntary Movement Scale(AIMS)2 times (Before treatment,immediately after treatment)

Secondary

MeasureTime frame
Change from baseline in intracortical facilitation(ICF)2 times (Before treatment,immediately after treatment)
Change from baseline in Simpson-Angus Scale(SAS)2 times (Before treatment,immediately after treatment)
Change from baseline in cortical silent period2 times (Before treatment,immediately after treatment)
Change from baseline in Positive and Negative Syndrome Scale(PANSS)2 times (Before treatment,immediately after treatment)
Change from baseline in clinical global impression (CGI)2 times (Before treatment,immediately after treatment)
Change from baseline in Barnes Akathisia Rating Scale(BARS)2 times (Before treatment,immediately after treatment)
Change from baseline in short interval intracortical inhibition(SICI)2 times (Before treatment,immediately after treatment)

Countries

China

Contacts

Primary ContactDengtang Liu
erliu110@126.com+86 21 64387250-73775

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026