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Repetitive Transcranial Magnetic Stimulation for the Treatment of Negative Symptoms in Schizophrenia Patients.

A Randomized Double-blind Controlled Study of Repetitive Transcranial Magnetic Stimulation (rTMS) for the Treatment of Negative Symptoms in Schizophrenia Patients.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02842034
Enrollment
60
Registered
2016-07-22
Start date
2016-07-31
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

Schizophrenia

Keywords

schizophrenia, rTMS

Brief summary

This study is to determine whether high frequency repetitive transcranial magnetic stimulation (rTMS) is effective in the treatment of negative symptoms in schizophrenia patients

Detailed description

The principal objective of this trial is to investigate the effect of high frequency rTMS on negative symptoms in schizophrenia.

Interventions

DEVICERepetitive Transcranial Magnetic Stimulation

Stimulate the dorsomedial prefrontal cortex for 4 weeks.

Sponsors

Shanghai Mental Health Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
15 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* The diagnosis of schizophrenia according to DSM-IV; * 18~55 years old; * schizophrenic illness duration longer than one year; * The sum of negative scores in the range Positive and negative symptom score (PANSS) must be 20 points or higher, at least one item from the area of negative symptoms (N1-N7) must be ≥ 4 points (at least moderate, clinically significant symptoms), and improvement in negative symptom-sum (measuring by PANSS) must be 10% or lower during the last two weeks before rTMS stimulation. * Have a stable and consistent drug treatment at least two weeks prior the rTMS treatment; * Able to adhere to the treatment schedule; * IQ≥80; * Dextromanual, normal vision and hearing; * Signed an informed consent

Exclusion criteria

* rTMS contraindications: intracranial metal substance, with heart pacemakers and cochlear implants, intracranial pressure; * Acute risk of suicide and impulse; * patients to be diagnosed according to DSM-IV for substance abused, development delayed; * suffering from serious physical disease and can not accept the treatment; * history of epileptic seizures or the presence of epileptic activity documented on the basis of EEG; * difficult to maintain the current drug treatment for at least 1 month; * undergoing ECT or MECT in last 3 months; * current treatment with anticonvulsant acting drugs such as anticonvulsants, benzodiazepines.

Design outcomes

Primary

MeasureTime frame
Change from baseline in clinical improvement of negative symptoms (Scale for Assessment of Negative Symptoms [SANS], and Positive and Negative Syndrome Scale [PANSS] negative symptoms subscale)3 times (Before treatment,immediately after treatment,4 weeks after treatment)

Secondary

MeasureTime frame
Change from baseline in Calgary Depression Scale for Schizophrenia [CDSS]3 times (Before treatment,immediately after treatment,4 weeks after treatment)
Change from baseline in Positive and Negative Syndrome Scale [PANSS] positive symptoms subscale3 times (Before treatment,immediately after treatment,4 weeks after treatment)
Change from baseline in clinical global impression [CGI]3 times (Before treatment,immediately after treatment,4 weeks after treatment)
Change from baseline in WHO Disability Assessment Schedule 2.0 [WHODAS 2.0]3 times (Before treatment,immediately after treatment,4 weeks after treatment)
Change from baseline in Simpson-Angus Scale [SAS]3 times (Before treatment,immediately after treatment,4 weeks after treatment)
Change from baseline in Clinician Rated Dimensions of Psychosis Symptom [CRDPS]3 times (Before treatment,immediately after treatment,4 weeks after treatment)

Other

MeasureTime frame
Change from baseline in Resting-state functional MRI:TR=2000 ms,TE=35 ms,FA=90,Matrix =64×64,Nex=1,FOV=256 mm,thickness=4 mm,Gap=0,scanning 33 slices。2 times (Before treatment,immediately after treatment)
Change from baseline in diffusion tensor imaging (DTI):TR=8500,TE=87, matrix size=64×64, FOV=230, slices thickness = 3 mm, diff directions=30,scanning 46 slices2 times (Before treatment,immediately after treatment)
Change from baseline in Magnetic Resonance Spectroscopy (MRS) of DMPFC2 times (Before treatment,immediately after treatment)
Change from baseline in Wechsler Working Memory3 times (Before treatment,immediately after treatment,4 weeks after treatment)
Change from baseline in Letter-Number Span3 times (Before treatment,immediately after treatment,4 weeks after treatment)

Countries

China

Contacts

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

Outcome results

None listed

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