Status:

COMPLETED

Modafinil as an Adjunctive on Cognitive Functioning in Patients With Schizophrenia

Lead Sponsor:

Laval University

Conditions:

Schizophrenia and Schizophrenia Spectrum Psychosis

Eligibility:

All Genders

18+ years

Phase:

PHASE1

PHASE2

Brief Summary

Patients suffering from schizophrenia and schizophrenia spectrum psychosis frequently experience cognitive impairments. Such deficits may affect memory, attention and executive function processes. Man...

Eligibility Criteria

Inclusion

  • To have a diagnosis of schizophrenia or schizophrenia spectrum psychosis (schizophreniform, schizoaffective, delusional trouble, brief psychosis), as defined in Diagnostic and statistical manual of mental disorders (\[DSM-IV\], American Psychiatric Association \[APA\], 1995);
  • To be 18 years old or more;
  • Psychotic symptoms must be stabilized with a second generation antipsychotic for at least 4 weeks i.e. no item on Positive And Negative Syndrome Scale (\[PANSS\], Kay, Opler, \& Fiszbein, 1987) positive subscale equal or superior to a score of 5.
  • Neurocognitive impairments are observed on attention measures. Participants will merit one or more result equal or lower to Z = -1,00 in at least one attention task.(Color trail test part A, MWCT, Stroop test, CPT-II).

Exclusion

  • To have a diagnosis of mental retardation (APA, 1994), or medical affection other than schizophrenia or schizophrenia spectrum psychosis, or neurological troubles that can lead to cognitive impairments (ex : temporal epilepsy);
  • To have a current diagnosis of panic disorder (DSM-IV);
  • To manifest an important suicidal potential according to the psychiatrist clinical judgment;
  • To suffer from unstable hypertension, cardiac arrhythmia or any other cardiac disorders;
  • To take medications, drugs and/or natural products that have a stimulant effect on the CNS (e.g., cocaine, methylphenidate); and
  • To be a pregnant woman, who breast-feed, or a woman who do not use an effective contraceptive (abstinence is considered like an effective method).

Key Trial Info

Start Date :

September 1 2005

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

Estimated Enrollment :

30 Patients enrolled

Trial Details

Trial ID

NCT00314639

Start Date

September 1 2005

Last Update

February 12 2009

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Centre Hospitalier Robert-Giffard

Québec, Quebec, Canada, G1J 2G3