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Effect of Intermittent Theta Burst Stimulation (iTBS) for Alleviating Symptoms of Schizophrenia Patients

Not Applicable
Completed
Conditions
Functional Magnetic Resonance Imaging
Transcranial Magnetic Stimulation
Schizophrenia
Interventions
Device: transcranial magnetic stimulation
Registration Number
NCT03868358
Lead Sponsor
WANG KAI
Brief Summary

To investigate the treatment effect of intermittent theta-burst transcranial magnetic stimulation on symptomatic relief of schizophrenia patients, and the underlying neural mechanism by functional MRI and the resting electroencephalogram

Detailed Description

All patients underwent a medical evaluation that included physical examination and routine laboratory studies before and after intermittent theta-burst transcranial magnetic stimulation (iTBS) treatment. Patients were randomly allocated to iTBS group and the sham group by coin toss. There are about 30 patients in each group.The decision to enroll a patient was always made prior to randomization. Patients were studied using a double-blind design. Study participants, clinical raters, and all personnel responsible for the clinical care of the patient remained masked to allocated condition and allocation parameters. Only iTBS administrators had access to the randomization list; they had minimal contact with the patients, and no role in assessing the Positive and Negative Syndrome Scale (PANSS). Each patient would be treated for continuous 14 days by iTBS.Before the iTBS treatment, PANSS and Clinical Global Impression-severity of illness (CGI-SI) at baseline were obtained by a trained investigator to assess baseline severity of their symptoms. Scale for the Assessment of Negative Symptoms (SANS) and Scale for Assessment of Positive Symptoms (SAPS) were respectively supplemented to evaluate the severity of symptoms in different dimensions,.The patients had receiving a battery measure of neuropsychological tests (standardized tests to investigate their cognitive problems, anxiety and depressive symptoms in daily life), magnetic resonance imaging scan in multimodalities, electroencephalography (EEG), event-related potentials during stop signal test and Iowa-gambling test record. Other behavioral tests including intertemporal decision,spatial n-back test record.

After the last treatment, the Positive and Negative Syndrome Scale were obtained, as well as the Global Index of Safety to assess adverse events of the treatment. Patients were instructed to focus their answers on the past 14 days. The patients had also receiving a battery measure of neuropsychological tests, magnetic resonance imaging scan in multimodalities, and EEG record.Clinical Global Impression-global improvement (CGI-GI), Clinical Global Impression-efficacy index (CGI-EI) were evaluated at the end of treatment.

40-60 days after the last treatment, participants were interviewed to obtain the Positive and Negative Syndrome Scale,SAPS,SANS and HAMA,HAMD. They were instructed to focus their answers on the past week. Additionally, they were also asked to assess the battery of neuropsychological tests, and have magnetic resonance imaging scan in multimodalities, and EEG record. Afterwards, they were unblinded by the study coordinator.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Patients met diagnostic criteria for schizophrenia or schizoaffective disorder using the Structural Clinical Interview for Diagnostic and Statistical Manual Diploma in Social Medicine (DSM)-IV (SCID, Version 2.0).
  • Patients remain their psychotropic medication at steady dosages for at least 4 weeks prior to study entry and for the duration of the trial.
  • Verbal intelligence quotient > 85 as measured by using a Chinese version of the National Adult Reading Test.
Exclusion Criteria
  • History of significant head trauma or neurological disorders
  • Alcohol or drug abuse Focal brain lesions on T1- or T2-weighted fluid-attenuated inversion-recovery magnetic resonance images
  • a prior history of a seizure not induced by drug withdrawal,first degree relative with epilepsy, significant neurological illness or head trauma, endocrine disease, such as thyroid disease, significant unstable medical condition, recent aggression or other forms of behavioral dyscontrol
  • left-handedness, pregnancy
  • estimated intelligence quotient<80
  • current alcohol or drug abuse
  • inability to provide informed consent.
  • Hamilton Anxiety Rating Scale or the Hamilton Depression Rating Scale score > 14

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Sham Stimulationtranscranial magnetic stimulationSham Stimulation:no stimulation.Participants will receive sham TMS once daily for two weeks
Real Stimulationtranscranial magnetic stimulationReal Stimulation: active transcranial magnetic stimulation(Intermittent Theta Burst Stimulation).Participants will receive active TMS once daily for two weeks
Primary Outcome Measures
NameTimeMethod
Positive And Negative Syndrome Scale(PANSS)Baseline and 2 weeks post-treatment,and follow-up

The improvment in PANSS scores will constitute the major research outcome measure used to assess response to rTMS,reflecting the symptom improvment in patients

Secondary Outcome Measures
NameTimeMethod
Scale for the Assessment of Negative Symptoms (SANS)Baseline and 2 weeks post-treatment and follow-up

The improvment in SANS scores will constitute the major research outcome, and specifically reflect the degree of improvement in patients' negative symptoms

Functional connectivity change of transcranial magnetic stimulation(iTBS and sham)Baseline and 2 weeks post-treatment

Functional MRI measures: the functional connectivity between stimulated target and the whole brain areas

Scale for the Assessment of Positive Symptoms (SAPS)Baseline and 2 weeks post-treatment and follow-up

The improvment in SAPS scores will constitute the major research outcome, and specifically reflect the degree of improvement in patients' positive symptoms

EEG change of transcranial magnetic stimulation(iTBS and sham)Baseline and 2 weeks post-treatment

EEG measures: brain areas wave change of stimulation(iTBS and sham)

Multidimensional Empathy TestBaseline and 2 weeks post-treatment

Multidimensional empathy Test is associated with the function of left dorsolateral prefrontal cortex

Intertemporal decision testBaseline and 2 weeks post-treatment

Intertemporal decision test is associated with the function of left dorsolateral prefrontal cortex

Spatial n-back testBaseline and 2 weeks post-treatment

Spatial n-back test will reflect the prefrontal function

Trial Locations

Locations (1)

Anhui Medical University

🇨🇳

Hefei, Anhui, China

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