PREVENTING MORBIDITY IN FIRST EPISODE SCHIZOPHRENIA

Information

  • Research Project
  • 6538961
  • ApplicationId
    6538961
  • Core Project Number
    R01MH060004
  • Full Project Number
    5R01MH060004-05
  • Serial Number
    60004
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/30/1998 - 27 years ago
  • Project End Date
    5/31/2005 - 20 years ago
  • Program Officer Name
    HSIAO, JOHN
  • Budget Start Date
    6/1/2002 - 23 years ago
  • Budget End Date
    5/31/2005 - 20 years ago
  • Fiscal Year
    2002
  • Support Year
    5
  • Suffix
  • Award Notice Date
    5/16/2002 - 23 years ago

PREVENTING MORBIDITY IN FIRST EPISODE SCHIZOPHRENIA

DESCRIPTION (Applicant's Description): Our long-term studies of first episode schizophrenia patients have clearly indicated excellent initial responsiveness of positive psychotic symptoms to treatment with conventional antipsychotic medications. However, in the years immediately following this initial good response, morbidity increases: cognitive functioning improves with treatment but remains impaired in multiple domains, social/occupational adjustment is poor or worse for 25% of the patients, 15% develop a deficit state and the incidence of tardive dyskinesia is 6% per year of conventional antipsychotic exposure. Relapses, often multipl ones, are the rule and are usually precipitated by medication noncompliance. Prevention of this morbidity is the major clinical challenge in treating first episode patients and is the focus of this application. There is some evidence that the second generation antipsychotic drugs may have superior efficacy in terms of these outcome domains. However, these newer agents have been studied primarily in chronic and/or treatment resistant patient samples and there are virtually no long term studies or studies comparing the new drugs with one another. We propose to study them in the population that has the potential for maximum responsiveness and long-term benefit-patients with schizophrenia who are being treated for the first time. Specifically, we will randomly assign first episode patients to treatment with olanzapine, risperidone or ziprasidone. Treatment will be for 3 years. Outcome measures for the initial episode will include psychopathology (positive, negative and affective symptoms), side effects, neurocognition (executive function, memory and attention), social and occupational function and service utilization. The effects on long term course will be measured in terms of frequency and timing of relapses, level of recovery from subsequent episodes and prospectively assessed course of psychopathology, neurocognitive function, social/vocational function and service utilization. The results will provide a basis for informed treatment choices for clinicians as well as address the crucial question of the potential of the new treatments to improve the longitudinal course of this devastating illness.

IC Name
NATIONAL INSTITUTE OF MENTAL HEALTH
  • Activity
    R01
  • Administering IC
    MH
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    793879
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    242
  • Ed Inst. Type
  • Funding ICs
    NIMH:793879\
  • Funding Mechanism
  • Study Section
    ZMH1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    LONG ISLAND JEWISH MEDICAL CENTER
  • Organization Department
  • Organization DUNS
  • Organization City
    NEW HYDE PARK
  • Organization State
    NY
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    11040
  • Organization District
    UNITED STATES