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Modafinil Effects on Cognition in Schizophrenia Patients

A Dose-response Study of Modafinil Effects on Cognition in Schizophrenia Patients.

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00711464
Acronym
InO
Enrollment
29
Registered
2008-07-08
Start date
2008-05-31
Completion date
2012-07-31
Last updated
2017-09-29

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

Conditions

Schizophrenia

Keywords

cognition, pharmacology, memory, attention

Brief summary

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.

Detailed description

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.

Interventions

DRUGmodafinil (M1, M2, M4)

modafinil 100, 200, and 400 mg oral dose

Sponsors

University of California, Los Angeles
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 54 Years
Healthy volunteers
Yes

Inclusion criteria

* adults age 18-54 * diagnosis of schizophrenia or schizoaffective disorder, or healthy with no personal or family history of mental illness * able to provide informed consent

Exclusion criteria

* history of significant head injury or other neurological illness * active psychiatric illness requiring significant acute care * significant intellectual impairment (e.g. standardized full-scale IQ \< 70) * history of medical illness or treatment that is associated with significant increase in risk from modafinil treatment (e.g. cardiac disease) * significant active substance abuse * active pregnancy * active treatment with medications that have drug interactions with modafinil

Design outcomes

Primary

MeasureTime frameDescription
Cognitive Performance3-5 hoursPercent Accuracy on high-control (i.e. difficult) condition on test of cognitive control

Secondary

MeasureTime frameDescription
Systolic Blood Pressure3-5 hourssystolic blood pressure in mm Hg
Heart Rate3-5 hoursbeats per minute

Countries

United States

Participant flow

Participants by arm

ArmCount
All Participants
modafinil (M1, M2, M4): modafinil 100, 200, and 400 mg oral dose, and placebo, in random sequence.
29
Total29

Baseline characteristics

CharacteristicAll Participants
Age, Continuous31 years
STANDARD_DEVIATION 9
Ethnicity (NIH/OMB)
Hispanic or Latino
2 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
27 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Asian
3 Participants
Race (NIH/OMB)
Black or African American
6 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
White
20 Participants
Region of Enrollment
United States
29 participants
Sex: Female, Male
Female
8 Participants
Sex: Female, Male
Male
21 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
0 / 290 / 290 / 290 / 29
other
Total, other adverse events
0 / 290 / 290 / 290 / 29
serious
Total, serious adverse events
0 / 290 / 290 / 290 / 29

Outcome results

Primary

Cognitive Performance

Percent Accuracy on high-control (i.e. difficult) condition on test of cognitive control

Time frame: 3-5 hours

ArmMeasureValue (MEAN)Dispersion
100 mgCognitive Performance76.7 percentage correct of all trialsStandard Deviation 22.8
200 mgCognitive Performance75.5 percentage correct of all trialsStandard Deviation 26.8
400 mgCognitive Performance67.2 percentage correct of all trialsStandard Deviation 33.2
PlaceboCognitive Performance77.1 percentage correct of all trialsStandard Deviation 26.3
Secondary

Heart Rate

beats per minute

Time frame: 3-5 hours

ArmMeasureValue (MEAN)Dispersion
100 mgHeart Rate74 beats per minuteStandard Deviation 10
200 mgHeart Rate81 beats per minuteStandard Deviation 12
400 mgHeart Rate86 beats per minuteStandard Deviation 16
PlaceboHeart Rate76 beats per minuteStandard Deviation 12
Secondary

Systolic Blood Pressure

systolic blood pressure in mm Hg

Time frame: 3-5 hours

ArmMeasureValue (MEAN)Dispersion
100 mgSystolic Blood Pressure109 mm HgStandard Deviation 16
200 mgSystolic Blood Pressure112 mm HgStandard Deviation 14
400 mgSystolic Blood Pressure116 mm HgStandard Deviation 16
PlaceboSystolic Blood Pressure111 mm HgStandard Deviation 10

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