Schizoaffective Disorder, Schizophrenia
Conditions
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
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.
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
Study design
Eligibility
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
| Measure | Time 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
| Measure | Time frame |
|---|---|
| Social Functioning | At baseline, every 2 weeks during rTMS sessions, and at monthly follow-up visits. |
| Depression | At baseline, every 2 weeks during rTMS sessions, and at monthly follow-up visits. |
| Theory of Mind | At baseline and the end of each study phase (random and open) |
| Global Clinical Improvement | At baseline, every 2 weeks during rTMS sessions, and at monthly follow-up visits. |
| Cognitive Function | At baseline, the first and last rTMS sessions of each study phase (random and open), and at monthly follow-up visits. |
| Cortical Excitability | At baseline, every 2 weeks during rTMS sessions, and at monthly follow-up visits. |
| Smoking Behaviors | At 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
| Arm | Count |
|---|---|
| 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 |
| Total | 0 |
Baseline characteristics
| Characteristic | — |
|---|---|
| Region of Enrollment United States | — participants |
Adverse events
| Event type | EG000 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 / 0 | 0 / 0 | 0 / 0 | 0 / 0 |
| serious Total, serious adverse events | 0 / 0 | 0 / 0 | 0 / 0 | 0 / 0 |
Outcome results
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.
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.
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.
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.
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.
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.
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.
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.