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Modafinil Effects on Cognition in Schizophrenia Patients (InO)

Primary Purpose

Schizophrenia

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
modafinil (M1, M2, M4)
Sponsored by
University of California, Los Angeles
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring cognition, pharmacology, memory, attention

Eligibility Criteria

18 Years - 54 Years (Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • University of California, Los Angeles
  • University of California, Davis School of Medicine

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Placebo Comparator

Arm Label

100 mg

200 mg

400 mg

Placebo

Arm Description

modafinil 100 milligrams oral dose

modafinil 200 mg oral dose

modafinil 400 mg oral dose

Single oral placebo capsule

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Systolic Blood Pressure
systolic blood pressure in mm Hg
Heart Rate
beats per minute

Full Information

First Posted
July 2, 2008
Last Updated
August 31, 2017
Sponsor
University of California, Los Angeles
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1. Study Identification

Unique Protocol Identification Number
NCT00711464
Brief Title
Modafinil Effects on Cognition in Schizophrenia Patients
Acronym
InO
Official Title
A Dose-response Study of Modafinil Effects on Cognition in Schizophrenia Patients.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2017
Overall Recruitment Status
Completed
Study Start Date
May 2008 (undefined)
Primary Completion Date
July 2012 (Actual)
Study Completion Date
July 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Los Angeles

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia
Keywords
cognition, pharmacology, memory, attention

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
29 (Actual)

8. Arms, Groups, and Interventions

Arm Title
100 mg
Arm Type
Experimental
Arm Description
modafinil 100 milligrams oral dose
Arm Title
200 mg
Arm Type
Experimental
Arm Description
modafinil 200 mg oral dose
Arm Title
400 mg
Arm Type
Experimental
Arm Description
modafinil 400 mg oral dose
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Single oral placebo capsule
Intervention Type
Drug
Intervention Name(s)
modafinil (M1, M2, M4)
Other Intervention Name(s)
Provigil
Intervention Description
modafinil 100, 200, and 400 mg oral dose
Primary Outcome Measure Information:
Title
Cognitive Performance
Description
Percent Accuracy on high-control (i.e. difficult) condition on test of cognitive control
Time Frame
3-5 hours
Secondary Outcome Measure Information:
Title
Systolic Blood Pressure
Description
systolic blood pressure in mm Hg
Time Frame
3-5 hours
Title
Heart Rate
Description
beats per minute
Time Frame
3-5 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
54 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael J. Minzenberg, MD
Organizational Affiliation
University of California, Los Angeles
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, Los Angeles
City
Los Angeles
State/Province
California
ZIP/Postal Code
90024
Country
United States
Facility Name
University of California, Davis School of Medicine
City
Sacramento
State/Province
California
ZIP/Postal Code
95817
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Modafinil Effects on Cognition in Schizophrenia Patients

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