The primary purpose of this study is to determine whether naltrexone is effective in the treatment of alcohol dependence and abuse in patients with schizophrenia and schizoaffective disorder. Hypotheses are as follows:

hypothesis 1: Naltrexone will be more effective than placebo in reducing alcohol use.

hypothesis 2: Patients responding to naltrexone by reducing alcohol use will also show reductions in severity of psychiatric symptoms and utilization of inpatient and emergency psychiatric services.

hypothesis 3: Severity of psychiatric symptoms and amount of service utilization will correlate positively with alcohol use.

Condition	Intervention	Phase
Schizophrenia Mental Disorders Alcohol Abuse Alcoholism Alcohol-Related Disorders	Drug: Naltrexone	Phase IV

Further Study Details: 

Primary Outcomes: Measures of Alcohol Use; Psychiatric Symptom Severity
Expected Total Enrollment:  150

The long-term goal of the proposed project is to improve the treatment of alcohol abuse and dependence in patients with schizophrenia and schizoaffective disorder. Alcohol use disorders are common among patients with severe mental illness. It is estimated that there may be as many as 750,000 individuals in the United States with comorbid schizophrenia and alcohol disorders. Alcohol disorder comorbidity requires treatment because it is associated with adverse consequences such as increased rates of hospitalization. Yet, to date, there are no reports of controlled trials testing the efficacy of pharmacological treatments for alcohol abuse or dependence in this population. Naltrexone pharmacotherapy is an effective treatment for alcohol dependence, but it has not been systematically applied to the care of patients with schizophrenia. The specific aims of this study are: To test the efficacy of naltrexone in reducing alcohol use among individuals with schizophrenia and schizoaffective disorder who also have alcohol abuse or dependence. We will test hypothesis 1: Naltrexone will be more effective than placebo in reducing alcohol use. Our primary outcome measure will be the number of drinking days over the course of the treatment trial. To test naltrexone''''s efficacy in reducing psychiatric symptom severity and medical utilization by reducing alcohol use. We will test hypothesis 2: Patients responding to naltrexone by reducing alcohol use will also show reductions in severity of psychiatric symptoms and utilization of inpatient and emergency psychiatric services. To determine the relationship between a) changes in alcohol use, and b) psychiatric symptom severity and inpatient and emergency service utilization. We will test hypothesis 3: Severity of psychiatric symptoms and amount of service utilization will correlate positively with alcohol use. The proposed research will study a cohort of 150 subjects in a double-blind, randomized, placebo-controlled trial of naltrexone using three times per week directly observed administration of medication. The study will be 6 months in duration, consisting of a 12-week course of naltrexone or placebo plus 3 monthly follow-up interviews after discontinuation of medication. Voucher incentives contingent on attendance will be provided to all subjects to ensure attendance for medication administration. Weekly motivational enhancement counseling sessions will also be provided to all subjects. Study outcomes will consist of self-report and biological measures of alcohol use as well as measures of psychiatric symptom severity and medical service utilization.

Ages Eligible for Study:  19 Years   -   69 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

1. Males or females, age 18 to 69, with a DSM-IV diagnosis of Schizophrenia or Schizoaffective Disorder;
2. DSM-IV diagnosis of Alcohol Abuse or Alcohol Dependence;
3. Level of Drinking: At least four days of drinking in the 30 days prior to consent;
4. Currently prescribed antipsychotic medication;
5. Currently involved in outpatient psychiatric treatment at one of the study sites (Hutchings Psychiatric Center, St. Joseph''''s Hospital Health Center, VA Medical Center) or at another location in the community at the time of randomization.

Exclusion Criteria:

1. Inability to give adequate informed consent;
2. Currently taking disulfiram (Antabuse) or naltrexone (ReVia/Depade);
3. Current DSM-IV diagnosis of Opioid Dependence or Opioid Abuse;
4. Currently taking ibuprofen or other potentially hepatotoxic medications in amount and/or frequency judged by the Principal Investigator to pose clinically significant added risk of hepatic injury;
5. Current use of prescribed or non-prescribed opioid analgesics, such as methadone, morphine, codeine, heroin, meperidine, and all other opioids.
6. Female patients of childbearing potential who are sexually active, not sterile, and who deny using a form of birth control;
7. Female patients who are pregnant or nursing;
8. Significant unstable medical problems, including any significant unstable psychiatric disorders. The study physician conducting the medical history and physical exam will exclude such clinically unstable individuals;
9. AST levels greater than 3x upper limit of normal;
10. Subjects who do not attend required screening appointments. Subsequent exclusion from the study for reasons related to non-attendance will be based on the judgment of the principal investigator;
11. In need of acute medical detoxification from alcohol in the judgment of the study physician based on results from the Clinical Institute Withdrawal Assessment of Alcohol Scale Based on DSM-III-R (CIWA-AD) and other information obtained;
12. Scheduled surgery within 3 months of intake;
13. Subjects who have pending legal proceedings whose outcome may lead to incarceration within 3 months of intake.

Please refer to this study by ClinicalTrials.gov identifier  NCT00145847

Jacqueline A Dimmock, Ph.D.      (315) 464-3133    dimmockj@upstate.edu
Michelle Bowman, B.A.      (315) 464-3171    BowmanM@upstate.edu

New York
      SUNY Upstate Medical University, Syracuse,  New York,  13210,  United States; Recruiting
      Hutchings Psychiatric Center, Syracuse,  New York,  13210,  United States; Recruiting
      St. Joseph''''s Mental Health Services, Syracuse,  New York,  13203,  United States; Recruiting
      Veterans Administration Healthcare Center, Syracuse,  New York,  13210,  United States; Recruiting

Study chairs or principal investigators

Steven L Batki, MD,  Principal Investigator,  State University of New York - Upstate Medical University   

Study ID Numbers:  SUNY UMU IRB # 4800; 1R01AA013655-01A1
Last Updated:  September 2, 2005
Record first received:  September 1, 2005
ClinicalTrials.gov Identifier:  NCT00145847
Health Authority: United States: Institutional Review Board
ClinicalTrials.gov processed this record on 2005-09-06