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Study of Repetitive Transcranial Magnetic Stimulation in the Treatment of Cognitive Impairment in Schizophrenia

S

Shanghai Mental Health Center

Status

Completed

Conditions

Schizophrenia

Treatments

Device: Repetitive Transcranial Magnetic Stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT01940939
11ZR1431600

Details and patient eligibility

About

  1. Exploration of repetitive transcranial magnetic stimulation(rTMS)on working memory and cognitive impairment symptoms of schizophrenia treatment and mechanism.
  2. Analysis of high-frequency repetitive transcranial magnetic stimulation stimulation to the improvement of negative symptoms and psychotic symptoms.

Full description

The study was a randomized double-blind sham-controlled trial for 4 weeks. Patients with schizophrenia were treated with 20-Hz rTMS for 4 weeks to the left dorsolateral prefrontal cortex (added to the ongoing treatment). Negative symptoms were assessed with the Scale for the Assessment of Negative Symptoms (SANS), the Positive and Negative symptom scale (PANSS).The auditory steady state responses (ASSR) were obtained for the assessment of gamma oscillation.And cognitive symptoms were assessed by MATRICS cognitive test battery (MCCB) Chinese version and n-back task.

Enrollment

70 patients

Sex

All

Ages

20 to 49 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 1)patients to be diagnosed according to the Fourth Edition of the Diagnostic and Statistical Manual of Mental Disorders(DSM-IV) for paranoid schizophrenia;2)20~49 years old;3)Duration of 2 ~ 10 years;4)the disease situation is stable, the fluctuation of Positive and Negative Symptom Scale(PANSS)total score ≤10% in last 1 month, and have accepted the current drugs for more than 8 weeks; 5)Patients, their families and doctors are agreed that the disease situation is stable and maintained current drug treatment in next month;6)Signed an informed consent

Exclusion criteria

  • 1)patients to be diagnosed according to DSM-IV for substance abused,development delayed;2)suffering from serious physical disease and can not accept the treatment;3)repetitive transcranial magnetic stimulation(rTMS) contraindications: intracranial metal substance, with heart pacemakers and cochlear implants, intracranial pressure;4)the disease situation is not stable, the fluctuation of Positive and Negative Symptom Scale(PANSS)total score >10% in last 1 month, Positive and Negative Symptom Scale(PANSS)total score > 60;5)difficult to maintain the current drug treatment for at least 1 month;6)undergoing electroconvulsive therapy(ECT)in last 3 months.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

70 participants in 2 patient groups

Active rTMS
Active Comparator group
Description:
Active treatment will be delivered at an intensity that is 90% of the resting motor threshold (RMT). Stimulation will be delivered at 20 Hz with 100 stimulation trains of 20 stimuli each (i.e., 2000 stimuli) and an inter-train interval of 9 sec. Treatment will be applied in sequential order to the left dorsolateral prefrontal cortex (DLPFC). Intervention: Device: Repetitive Transcranial Magnetic Stimulation
Treatment:
Device: Repetitive Transcranial Magnetic Stimulation
Sham rTMS
Sham Comparator group
Description:
Sham rTMS stimulation will be delivered using the same stimulation parameters and at the site of active treatment, but the coil will be reversed. This method produces sound and some somatic sensation (e.g., contraction of scalp muscles) similar to those of active stimulation, but with minimal direct brain effects.Intervention: Device: Repetitive Transcranial Magnetic Stimulation
Treatment:
Device: Repetitive Transcranial Magnetic Stimulation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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