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A Dose-Response Study of Modafinil Effects on Cognition in Healthy Adults and in Schizophrenia Patients (InO)
This study is currently recruiting participants.
Study NCT00711464   Information provided by University of California, Davis
First Received: July 2, 2008   Last Updated: February 18, 2009   History of Changes

July 2, 2008
February 18, 2009
May 2008
July 2010   (final data collection date for primary outcome measure)
cognitive performance [ Time Frame: 3-5 hours ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00711464 on ClinicalTrials.gov Archive Site
  • blood pressure [ Time Frame: 3-5 hours ] [ Designated as safety issue: No ]
  • heart rate [ Time Frame: 3-5 hours ] [ Designated as safety issue: No ]
Same as current
 
A Dose-Response Study of Modafinil Effects on Cognition in Healthy Adults and in Schizophrenia Patients
A Dose-Response Study of Modafinil Effects on Cognition in Healthy Adults and in Schizophrenia Patients.

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 will also enroll healthy adults in these same procedures in order to determine how these effects are manifest in normal-range cognitive function. We predict that when patients or control participants receive modafinil, they will perform better on cognitive tests, 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 these processes in healthy adults, in order to evaluate modafinil effects on normal-range cognition, and then evaluate the remediation of deficits in these functions 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.

Phase IV
Interventional
Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Uncontrolled, Single Group Assignment, Efficacy Study
Schizophrenia
Drug: modafinil (M1, M2, M4)
  • Experimental: modafinil 100 milligrams oral dose
  • Experimental: modafinil 200 mg oral dose
  • Experimental: modafinil 400 mg oral dose
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
80
July 2010
July 2010   (final data collection date for primary outcome measure)

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
Both
18 Years to 54 Years
Yes
Contact: Michael J Minzenberg, MD 916-734-7174 michael.minzenberg@ucdmc.ucdavis.edu
Contact: Janeth Nunez-Prado, BA 916-734-3668 janeth.nunez@ucdmc.ucdavis.edu
United States
 
NCT00711464
Michael J. Minzenberg, MD; Assistant Professor, University of California, Davis School of Medicine
200715868-1
University of California, Davis
 
Principal Investigator: Michael J. Minzenberg, MD University of California, Davis
University of California, Davis
February 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP