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Original Articles

Dissociating medication effects from learning and practice effects in a neurocognitive study of schizophrenia: Olanzapine versus haloperidol

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Pages 322-338 | Received 12 Apr 2006, Published online: 05 Jun 2007
 

Abstract

Objective. To contrast the effect of a typical antipsychotic (haloperidol) and an atypical antipsychotic (olanzapine) on neurocognitive functioning in schizophrenia when learning and practice (LP) effects are controlled.

Methods. Two groups of participants were recruited, 27 schizophrenia patients in their first 5 years of illness and 13 normal controls. Prior to double-blind randomisation, all subjects were assessed on four occasions within 5 days (prerandomisation period) on the same neurocognitive battery. Repeated assessment prior to randomisation was chosen as a method to control for LP effects. Patients were then randomised to 56 days of treatment with haloperidol or olanzapine (postrandomisation). All subjects were assessed on neurocognitive measures at Days 28 and 56.

Results. LP effects were present during the prerandomisation period on motor tasks, verbal and visual short-term memory, attention, and on a measure of verbal working memory. There were no changes in performance for patients randomised to treatment with olanzapine or haloperidol or the normal control group during the postrandomisation period.

Conclusions. Once LP effects are controlled, olanzapine and haloperidol do not affect performance on measures of motor functioning, verbal short-term memory, attention, verbal working memory, reaction time, visuospatial short-term memory, and visual working memory beyond that observed from LP effects.

Acknowledgements

The authors wish to thank Dr Helen Ward for her assistance with this research. This work was completed by Dr Luc J. Boulay as a dissertation project at Carleton University in Ottawa Canada. This work was carried out at the Royal Ottawa Hospital. Partial financial support was provided by Eli Lilly Canada through an investigator initiated grant (Zyprexa Research Fund: Grant F1D-CA-O045).

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