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Patients with schizophrenia have problems in thinking, known as cognitive dysfunction. This includes many types of cognitive dysfunction, such as in attention, memory and language. These problems may explain why patients with schizophrenia think and act in unusual ways, and often have problems managing aspects of their lives that healthy adults take for granted. Unfortunately, the biochemical aspects of these dysfunctions are presently unknown, and it is not clear whether current psychiatric medications can improve these functions. A recent FDA-approved medication that may improve this function is modafinil. Studies in animals and healthy adults show that this medication can improve many of these cognitive functions. We plan to study the effects of modafinil on these cognitive processes, by giving various doses of this medication to patients before they perform tasks of these cognitive processes. We predict that when patients receive modafinil, they will perform better on a cognitive test, and that these benefits will depend on the dose given.
Schizophrenia is a disorder of cognition. The cognitive deficits of schizophrenia are present at the onset of the disorder, prior to medication exposure, are persistent during periods of remission, and are strongly related to functional outcome. These deficits prominently include prefrontal cortex-dependent functions. While existing medications effectively treat psychotic symptoms, they exhibit modest benefit at best for cognitive dysfunction. Studies of cognition in animal models indicate that the neurotransmitter systems that mediate many cognitive processes are not generally augmented by existing antipsychotic medications. Therefore, advances in the treatment of schizophrenia will require the study of agents with novel pharmacological profiles to establish their potential to remediate cognitive dysfunction.
This study will evaluate the effects of modafinil on the range of cognitive processes known to be disturbed in schizophrenia. Modafinil is an FDA-approved medication with a unique pharmacological profile and an increasing range of off-label indications. Its neurochemical effects in animal models include elevation of extracellular dopamine (DA), noradrenaline (NA) and glutamate in the neocortex. This profile is favorable for the enhancement of cognitive processes. These neurochemical effects also appear to be selective for cortical versus subcortical brain regions, suggesting that modafinil may have minimal effects on psychotic symptoms, or extrapyramidal, autonomic and hormonal side effects. In addition, it differs from amphetamine in structure, neurochemical profile and behavioral effects, with a lower risk of addictive or cerebrovascular effects. Recent studies in animal models, healthy adults and adults with psychiatric and neurological disorders indicate that modafinil improves prefrontal cognitive functions. This suggests that modafinil is a leading candidate for the treatment of cognitive dysfunction in schizophrenia. We aim to test modafinil effects on the remediation of deficits in cognition in individuals with schizophrenia. We will vary the dose within each participant to evaluate dose-response relationships, and directly compare cognition outcome measures for sensitivity to drug effects.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 100 mg | Experimental | modafinil 100 milligrams oral dose |
|
| 200 mg | Experimental | modafinil 200 mg oral dose |
|
| 400 mg | Experimental | modafinil 400 mg oral dose |
|
| Placebo | Placebo Comparator | Single oral placebo capsule |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| modafinil (M1, M2, M4) | Drug | modafinil 100, 200, and 400 mg oral dose |
|
| Measure | Description | Time Frame |
|---|---|---|
| Cognitive Performance | Percent Accuracy on high-control (i.e. difficult) condition on test of cognitive control | 3-5 hours |
| Measure | Description | Time Frame |
|---|---|---|
| Systolic Blood Pressure | systolic blood pressure in mm Hg | 3-5 hours |
| Heart Rate | beats per minute | 3-5 hours |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Michael J. Minzenberg, MD | University of California, Los Angeles | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of California, Los Angeles | Los Angeles | California | 90024 | United States | ||
| University of California, Davis School of Medicine |
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| ID | Title | Description |
|---|---|---|
| FG000 | All Participants | modafinil 100 milligrams oral dose, 200 milligrams oral dose, 400 milligrams oral dose, and placebo, in randomly sequenced dosing periods. |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | All Participants | modafinil (M1, M2, M4): modafinil 100, 200, and 400 mg oral dose, and placebo, in random sequence. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Cognitive Performance | Percent Accuracy on high-control (i.e. difficult) condition on test of cognitive control | Posted | Mean | Standard Deviation | percentage correct of all trials | 3-5 hours |
|
6 hours post-dose on treatment days
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | 100 mg | modafinil 100 milligrams oral dose | 0 |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Michael Minzenberg, MD | University of California, Los Angeles | (310) 825-7642 | MMinzenberg@mednet.ucla.edu |
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| ID | Term |
|---|---|
| D012559 | Schizophrenia |
| ID | Term |
|---|---|
| D019967 | Schizophrenia Spectrum and Other Psychotic Disorders |
| D001523 | Mental Disorders |
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| ID | Term |
|---|---|
| D000077408 | Modafinil |
| ID | Term |
|---|---|
| D001559 | Benzhydryl Compounds |
| D001555 | Benzene Derivatives |
| D006841 | Hydrocarbons, Aromatic |
| D006844 | Hydrocarbons, Cyclic |
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| Sacramento |
| California |
| 95817 |
| United States |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
modafinil 400 mg oral dose
modafinil (M1, M2, M4): modafinil 100, 200, and 400 mg oral dose
| OG003 | Placebo | Single oral placebo capsule modafinil (M1, M2, M4): modafinil 100, 200, and 400 mg oral dose |
|
|
| Secondary | Systolic Blood Pressure | systolic blood pressure in mm Hg | Posted | Mean | Standard Deviation | mm Hg | 3-5 hours |
|
|
|
| Secondary | Heart Rate | beats per minute | Posted | Mean | Standard Deviation | beats per minute | 3-5 hours |
|
|
|
| 29 |
| 0 |
| 29 |
| 0 |
| 29 |
| EG001 | 200 mg | modafinil 200 mg oral dose | 0 | 29 | 0 | 29 | 0 | 29 |
| EG002 | 400 mg | modafinil 400 mg oral dose | 0 | 29 | 0 | 29 | 0 | 29 |
| EG003 | Placebo | Single oral placebo capsule | 0 | 29 | 0 | 29 | 0 | 29 |
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| D006838 |
| Hydrocarbons |
| D009930 | Organic Chemicals |