Brain Activation Patterns in Schizophrenia After Computerized Cognitive Skills Training

Brief Summary

Official Title: “Does Computerized Cognitive Skills Training Change Brain Activation Patterns in Schizophrenia?”

This project is a novel exploratory research project to investigate changes in activation patterns of the dorsolateral prefrontal cortex (DLPFC) in inpatients with schizophrenia who received a 12-week computerized cognitive remediation (CRT) program. The hypothesis is that patients receiving CRT will show greater increase in activation patterns in the brain as compared to controls, and the degree of brain activation will correlate with improvements in working memory.

  • Study Type: Interventional
  • Study Design: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Detailed Clinical Trial Description

Abnormalities in the domains of attention, working memory (WM) and information processing are important features of schizophrenia. There is growing literature that cognitive remediation therapy (CRT) can produce modest improvements in cognitive functioning in schizophrenia, suggesting that systematic efforts at improving cognitive functioning are feasible. Cognitive improvement after CRT may correlate with changes in brain activation patterns in specific areas.

After screening, patients are randomized to a 12 week trial of CRT using COGPACK (Marker Software), or to a 12-week control condition. All patients attend 3 weekly 1-hour laboratory sessions, with 1 discussion session per week.

Patients continue their antipsychotic treatment with a typical or atypical antipsychotic during the CRT and 4 weeks prior to enrollment in the study (Phase A). Following Phase A they receive baseline evaluations, including an cognitive activation task (N-back visual-letter task) while being scanned for fMRI , MATRICS neuropsychological test battery, and psychiatric, social functioning, and symptoms assessment.

Patients then enter Phase B with randomization to control or CRT for 12 weeks (36 laboratory sessions). Upon successful completion of 36 sessions, endpoint evaluations include an N-back task while fMRI scan, MATRICS, psychiatric, and social functional assessments.

All baseline and endpoint fMRI scans are conducted at the Center for Advanced Brain Imaging (CABI) at Nathan Kline Institute for Psychiatric Research.

Interventions Used in this Clinical Trial

  • Behavioral: Cognitive remediation therapy
    • 36 sessions of computerized cognitive skills training over a 12 week duration.
  • Other: No Computerized Cognitive Skills Training
    • Patients attend ‘treatment-as-usual’ mall program sessions, with similar clinician exposure time as the active group.

Arms, Groups and Cohorts in this Clinical Trial

  • Active Comparator: Active Group
  • No Intervention: Control Group

Outcome Measures for this Clinical Trial

Primary Measures

  • Brain activation changes after stimulation with a neurocognitive task in the dorso-lateral prefrontal cortex (DLPFC)
    • Time Frame: 12 weeks
      Safety Issue?: No

Secondary Measures

  • Examine the relationship of changes in DLPFC activation patterns in relation to improvement on neurocognitive tests
    • Time Frame: 12 weeks
      Safety Issue?: No

Criteria for Participation in this Clinical Trial

Inclusion Criteria

  • Inpatient status
  • Age 18 – 55
  • Male gender (females are enrolled but will not be scanned)
  • DSM-IV diagnosis of schizophrenia (all subtypes) and schizoaffective disorder
  • illness duration > 5 years
  • MMSE score > 24 (inclusive) at screening
  • Stable dose of oral atypical antipsychotic for at least 4 weeks prior to study entry
  • Total PANSS score > 60 at screening
  • Capacity and willingness to give written informed consent
  • Patients deemed not ready to be discharged within the next 12 weeks

Exclusion Criteria

  • Inability to read or speak English
  • Documented disease of the central nervous system
  • History of intellectual impairment pre-dating onset of symptoms of psychosis (e.g. mental retardation)
  • Clinically significant or unstable cardiovascular, renal, hepatic, gastrointestinal, pulmonary, or hematological conditions; HIV positive
  • Any medical condition rendering the subject unable to receive an fMRI scan

Gender Eligibility for this Clinical Trial: Male

Minimum Age for this Clinical Trial: 18 Years

Maximum Age for this Clinical Trial: 55 Years

Are Healthy Volunteers Accepted for this Clinical Trial: No

Clinical Trial Investigator Information

  • Lead Sponsor
    • Manhattan Psychiatric Center
  • Collaborator
    • Nathan Kline Institute for Psychiatric Research
  • Provider of Information About this Clinical Study
    • Saurabh Kaushik, Manhattan Psychiatric Center
  • Overall Official(s)
    • Saurabh Kaushik, MD, Principal Investigator, Manhattan Psychaitric Center
    • Jean-Pierre Lindenmayer, MD, Study Chair, Manhattan Psychiatric Center
    • Susan McGurk, PhD, Study Chair, Dartmouth College, Hanover
    • Craig A. Branch, PhD, Study Chair, Center for Advanced Brain Imaging, NKI

References

Wykes T, Reeder C, Corner J, Williams C, Everitt B. The effects of neurocognitive remediation on executive processing in patients with schizophrenia. Schizophr Bull. 1999;25(2):291-307.

Source

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The URL of this page is:
http://clinicaltrialsfeeds.org/clinical-trials/show/NCT00431223