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Repetitive Transcranial Magnetic Stimulation and Intermittent Theta Burst (iTBS) in Schizophrenia

A Double-blind Placebo Controlled Trial the Comparison of Effectiveness of Repetitive TMS and iTBS on Negative Symptoms and Cognition in Patients With Schizophrenia

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01315587
Enrollment
30
Registered
2011-03-15
Start date
2011-01-31
Completion date
2017-01-31
Last updated
2015-09-01

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

Conditions

Schizophrenia

Brief summary

The pilot studies have showed that theta burst stimulation (TBS) can have the more rapid and durable effects to the apply traditional rTMS protocols. The aim of this study is to investigate the effect of repetitive TMS and theta burst in reduction of negative symptoms and remission of cognitive functioning in patients with schizophrenia. In a randomized, double blind clinical trials, 30 patients with schizophrenia in Razi psychiatric hospital will be assigned to receive repetitive TMS; theta burst, or sham TMS, daily; for 20 sessions. The negative symptoms and cognitive functioning will be assessed before the treatment (pre test) during the treatment (session 10), and after the treatment (post test).QEEG and LORETA apply before and after rTMS in all subjects.

Interventions

DEVICErepetitive Transcranial Magnetic Stimulation (Magstim rapid2 )

* 3 pulses at 50Hz repeated each 200 ms for 2 seconds * 80% MT * 20 days treatment

DEVICErepetitive Transcranial Magnetic Stimulation (Magstim rapid2)

LDLPFC 110% MT 15 Hz 20 days

DEVICErepetitive Transcranial Magnetic Stimulation(Magstim rapid2)

Placebo treatment: Sham coil

Sponsors

University of Tehran
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

1. Outpatients male and female with the range of 18-50 years of age 2. The diagnosis of schizophrenia according to DSM-IV-TR 3. Completion of consent form 4. Being under supervision of a psychiatrist, 5. Being able to adhere to treatment schedule, 6. Having stable symptoms as defined by not requiring a change in antipsychotic medication for at least 4 weeks or at least 2 weeks for psychotropic agents prior to entering the Study

Exclusion criteria

1. The history of rTMS treatment for any reason 2. Cardiac pacemaker 3. Drug pumps 4. Acute heart attack 5. The risk of seizure with any reasons 6. The history of epilepsy or seizure in the first relatives 7. Any metal in head 8. Brain trauma 9. Pregnancy 10. Breastfeeding 11. Drug dependency

Design outcomes

Primary

MeasureTime frame
Positive and negative syndrome scale ( PANSS )Change of baseline in negative symptoms at 20 sessions

Secondary

MeasureTime frameDescription
Calgary depression for schizophrenia scale (CDSS)3 times (Before treatment, session 10, immediately after treatment)The CDSS is administered for measuring of depression before treatment, session 10, immediately after treatment
Schizophrenia quality of life scale (SQLS)3 times (Before treatment, session 10, immediately after treatment)The SQLS is administered for apprising of quality of life before treatment, session 10, immediately after treatment.
Cantab Schizophrenia Battery3 times (Before treatment, session 10, immediately after treatment)Cantab Schizophrenia Battery is included six tests, which is measuring for cognitive function. The cognitive function includes reaction time, executive function, Sustained attention, , Episodic memory . These scales: Reaction time (RTI) Rapid Visual information processing (RVP) Spatial Working Memory (SWM) One Touch Stockings of Cambridge (OTS) Paired Associates Learning (PAL) Intra-Extra Dimensional set- Shift (IED)
QEEG and low resolution brain electromagnetic tomography (LORETA)3 times (Before treatment,session 10, immediately after treatment)QEEG and LORETA is applying for assessment brain waves patterns.

Other

MeasureTime frame
Hamilton Depression Rating Scale (HAMD-17)3 times (Before treatment,session 10, immediately after treatment)

Countries

Iran

Contacts

Primary ContactReza kazemi, PhD
rezakazemi@ut.ac.ir009802184012128

Outcome results

None listed

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