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Treatment of Negative Symptoms of Schizophrenia With Transcranial Magnetic Stimulation (TMS)

Repetitive Transcranial Magnetic Stimulation (rTMS) in the Treatment of Negative Symptoms and Social Dysfunction in Schizophrenia Patients

Status
Terminated
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00517075
Enrollment
14
Registered
2007-08-16
Start date
2004-09-30
Completion date
2011-06-30
Last updated
2017-01-13

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

Conditions

Schizoaffective Disorder, Schizophrenia

Keywords

Transcranial Magnetic Stimulation, Repetitive Transcranial Magnetic Stimulation, Schizophrenia, Schizoaffective Disorder, Treatment, Negative Symptoms, Social Dysfunction, TMS, rTMS

Brief summary

This study will test whether repetitive transcranial magnetic stimulation (rTMS) is helpful in treating negative symptoms and social deficits of schizophrenia. This will be the first rTMS study to assess social function and social cognition. 1. Hypoactivity in the dorsolateral prefrontal cortex (DLPFC) has been implicated in generating the negative symptoms of schizophrenia. Abnormalities in the left inferior parietal lobe (IPL) have also been associated with negative symptoms. We hypothesize that high frequency rTMS applied to the hypoactive left DLPFC or to the left IPL in individuals with schizophrenia will reduce negative symptom severity more than sham (placebo) rTMS as assessed by the Positive and Negative Syndrome Scale (PANSS) negative symptoms subscale. 2. We hypothesize that high frequency rTMS applied to the left DLPFC or to the left IPL in schizophrenia patients will improve social dysfunction more than sham (placebo) rTMS as assessed by the Social Adjustment Scale, the Social Adaptation Self-Evaluation Scale and the Social Functioning Scale.

Detailed description

Most treatments for schizophrenia are helpful in treating positive symptoms (e.g. hallucinations), whereas negative symptoms (e.g. low social drive) are only partially responsive to medication. Repetitive transcranial magnetic stimulation (rTMS) is a noninvasive way of stimulating the brain that has been FDA approved for the treatment of depression and has shown promise in schizophrenia. In rTMS therapy, a device called a magnetic stimulator provides electrical energy to a magnetic coil that delivers a magnetic field. When the coil is placed against the surface of the head, the magnetic field can cause parts of the brain to either increase or decrease in activity, depending on how quickly the magnetic pulses are delivered. This study is designed to test whether high-frequency rTMS delivered to an area near the front of the head, called the dorsolateral prefrontal cortex, can improve the negative symptoms of schizophrenia, which include decreased thinking, difficulty motivating, and social withdrawal. Participation in the first phase of the study consists of sessions lasting about 45 minutes per day, 5 days a week, for 4 weeks. Twenty-four subjects will be randomly assigned to receive four weeks of either active (real) rTMS or inactive (sham) rTMS. Patients will receive magnetic resonance imaging (MRI) of their brains to help locate where the rTMS should be applied. Symptoms will be rated at baseline, during the rTMS course, and at the end of the 4 weeks. Patients who do not meet response criteria after the four weeks of the randomized phase will be offered active (real) daily rTMS for an additional four weeks in the open phase of the study. All patients will have two monthly repeat assessments after their last rTMS session to examine the persistence of benefit. We will also collect measures of motor cortex excitability (performed with single pulse TMS) at baseline, at the end of the randomized and, if applicable, the open study phase, and at each of the two follow-up assessments to determine whether changes in these measures correlate with clinical improvement. In addition, we will look at brain dynamics using electroencephalography (EEG) pre- and post-rTMS in the first and last sessions of each study phase. We will also assess the effects of rTMS on cigarette use, as schizophrenia patients are known to have increased prevalence of nicotine dependence. There is also preliminary evidence that high frequency rTMS to the left DLPFC decreases cigarette smoking.

Interventions

DEVICETranscranial Magnetic Stimulation (TMS)

For rTMS, the coil is held flat on the scalp. 40 trains of 10 Hz rTMS will be delivered in trains lasting 4 seconds, with an intertrain interval of 26 seconds, for a total of 20 minutes (1600 pulses per day) at 100% motor threshold. Subjects will receive rTMS once a day, 5 days a week, for 4 weeks. During the first week of rTMS sessions only, in the event that the patient cannot tolerate these stimulation parameters, intensity relative to motor threshold may be titrated downward, in a masked fashion, to 80%, with all other dose parameters remaining the same.

DEVICErepetitive transcranial magnetic stimulation

For rTMS, the coil is held flat on the scalp. 40 trains of 10 Hz rTMS will be delivered in trains lasting 4 seconds, with an intertrain interval of 26 seconds, for a total of 20 minutes (1600 pulses per day) at 100% motor threshold. Subjects will receive rTMS once a day, 5 days a week, for 4 weeks. During the first week of rTMS sessions only, in the event that the patient cannot tolerate these stimulation parameters, intensity relative to motor threshold may be titrated downward, in a masked fashion, to 80%, with all other dose parameters remaining the same.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
National Alliance for Research on Schizophrenia and Depression
CollaboratorOTHER
New York State Psychiatric Institute
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Male or female inpatients or outpatients, 18 to 55 years of age. * Primary diagnosis by DSM-IV criteria for Schizophrenia or Schizoaffective Disorder. * Capacity and willingness to give informed consent. * Engaged in ongoing treatment with a psychiatrist. * PANSS negative symptoms subscale score of ≥ 15. * English speaking. * Patients must have stable symptoms as defined by not requiring a change in antipsychotic medication for at least 4 weeks or at least 2 weeks for other psychotropic agents (e.g. antidepressants) prior to entering the study. Patients will not be included in the study if the research team thinks that modifications could be made to maximize their medication regimen at initial evaluation. * Able to adhere to the treatment schedule. * Able to commute to NYC for daily treatments (Monday - Friday) for at least 4 weeks.

Exclusion criteria

* Individuals diagnosed by the investigator with the following conditions (current unless otherwise stated): Current affective disorder including Major Depressive Disorder, Bipolar Affective Disorder; substance abuse or dependence within the past year (except nicotine and caffeine). * An Axis II Personality Disorder, which in the judgment of the investigator may hinder the patient in completing the procedures required by the study protocol. Other

Design outcomes

Primary

MeasureTime frame
Clinical Improvement of Negative Symptoms (Positive and Negative Syndrome Scale [PANSS] Negative Symptoms Subscale) Relative to Pre-treatment Baseline.At baseline, every 2 weeks during rTMS sessions, and at monthly follow-up visits.

Secondary

MeasureTime frame
Social FunctioningAt baseline, every 2 weeks during rTMS sessions, and at monthly follow-up visits.
DepressionAt baseline, every 2 weeks during rTMS sessions, and at monthly follow-up visits.
Theory of MindAt baseline and the end of each study phase (random and open)
Global Clinical ImprovementAt baseline, every 2 weeks during rTMS sessions, and at monthly follow-up visits.
Cognitive FunctionAt baseline, the first and last rTMS sessions of each study phase (random and open), and at monthly follow-up visits.
Cortical ExcitabilityAt baseline, every 2 weeks during rTMS sessions, and at monthly follow-up visits.
Smoking BehaviorsAt baseline, every 2 weeks during rTMS sessions, and at monthly follow-up visits.

Countries

United States

Participant flow

Recruitment details

P.I. has left the institution and NYSPI has no access to the data. Results will not be analyzed or presented.

Participants by arm

ArmCount
High Frequency rTMS
high frequency rTMS to the left infero-parietal lobe, active/sham condition randomized (2:1), double-blind Transcranial Magnetic Stimulation (TMS): For rTMS, the coil is held flat on the scalp. 40 trains of 10 Hz rTMS will be delivered in trains lasting 4 seconds, with an intertrain interval of 26 seconds, for a total of 20 minutes (1600 pulses per day) at 100% motor threshold. Subjects will receive rTMS once a day, 5 days a week, for 4 weeks. During the first week of rTMS sessions only, in the event that the patient cannot tolerate these stimulation parameters, intensity relative to motor threshold may be titrated downward, in a masked fashion, to 80%, with all other dose parameters remaining the same.
0
Active High Frequency rTMS
Active high frequency rTMS to the left dorsolateral prefrontal cortex Transcranial Magnetic Stimulation (TMS): For rTMS, the coil is held flat on the scalp. 40 trains of 10 Hz rTMS will be delivered in trains lasting 4 seconds, with an intertrain interval of 26 seconds, for a total of 20 minutes (1600 pulses per day) at 100% motor threshold. Subjects will receive rTMS once a day, 5 days a week, for 4 weeks. During the first week of rTMS sessions only, in the event that the patient cannot tolerate these stimulation parameters, intensity relative to motor threshold may be titrated downward, in a masked fashion, to 80%, with all other dose parameters remaining the same.
0
Sham/Placebo
Sham (placebo) high frequency rTMS to the left dorsolateral prefrontal cortex or left infero-parietal lobe, active/sham condition randomized (2:1), double-blind Transcranial Magnetic Stimulation (TMS): For rTMS, the coil is held flat on the scalp. 40 trains of 10 Hz rTMS will be delivered in trains lasting 4 seconds, with an intertrain interval of 26 seconds, for a total of 20 minutes (1600 pulses per day) at 100% motor threshold. Subjects will receive rTMS once a day, 5 days a week, for 4 weeks. During the first week of rTMS sessions only, in the event that the patient cannot tolerate these stimulation parameters, intensity relative to motor threshold may be titrated downward, in a masked fashion, to 80%, with all other dose parameters remaining the same.
0
Open Cross Over High Frequency rTMS
Following the randomization phase with three arms, subjects who did not respond, have the possibility of receiving open active treatment to the target that they did not receive treatment to in the randomization phase. (i.e. randomized to IPL --\> open phase DLPFC and vice versa) repetitive transcranial magnetic stimulation: For rTMS, the coil is held flat on the scalp. 40 trains of 10 Hz rTMS will be delivered in trains lasting 4 seconds, with an intertrain interval of 26 seconds, for a total of 20 minutes (1600 pulses per day) at 100% motor threshold. Subjects will receive rTMS once a day, 5 days a week, for 4 weeks. During the first week of rTMS sessions only, in the event that the patient cannot tolerate these stimulation parameters, intensity relative to motor threshold may be titrated downward, in a masked fashion, to 80%, with all other dose parameters remaining the same.
0
Total0

Baseline characteristics

Characteristic
Region of Enrollment
United States
— participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
EG003
affected / at risk
deaths
Total, all-cause mortality
— / —— / —— / —— / —
other
Total, other adverse events
0 / 00 / 00 / 00 / 0
serious
Total, serious adverse events
0 / 00 / 00 / 00 / 0

Outcome results

Primary

Clinical Improvement of Negative Symptoms (Positive and Negative Syndrome Scale [PANSS] Negative Symptoms Subscale) Relative to Pre-treatment Baseline.

Time frame: At baseline, every 2 weeks during rTMS sessions, and at monthly follow-up visits.

Population: P.I. has left the institution and NYSPI has no access to the data. Results will not be analyzed or presented.

Secondary

Cognitive Function

Time frame: At baseline, the first and last rTMS sessions of each study phase (random and open), and at monthly follow-up visits.

Population: P.I. has left the institution and NYSPI has no access to the data. Results will not be analyzed or presented.

Secondary

Cortical Excitability

Time frame: At baseline, every 2 weeks during rTMS sessions, and at monthly follow-up visits.

Population: P.I. has left the institution and NYSPI has no access to the data. Results will not be analyzed or presented.

Secondary

Depression

Time frame: At baseline, every 2 weeks during rTMS sessions, and at monthly follow-up visits.

Population: P.I. has left the institution and NYSPI has no access to the data. Results will not be analyzed or presented.

Secondary

Global Clinical Improvement

Time frame: At baseline, every 2 weeks during rTMS sessions, and at monthly follow-up visits.

Population: P.I. has left the institution and NYSPI has no access to the data. Results will not be analyzed or presented.

Secondary

Smoking Behaviors

Time frame: At baseline, every 2 weeks during rTMS sessions, and at monthly follow-up visits.

Population: P.I. has left the institution and NYSPI has no access to the data. Results will not be analyzed or presented.

Secondary

Social Functioning

Time frame: At baseline, every 2 weeks during rTMS sessions, and at monthly follow-up visits.

Population: P.I. has left the institution and NYSPI has no access to the data. Results will not be analyzed or presented.

Secondary

Theory of Mind

Time frame: At baseline and the end of each study phase (random and open)

Population: P.I. has left the institution and NYSPI has no access to the data. Results will not be analyzed or presented.

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