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Comparison of Optimal Antipsychotic Treatments for Adults With Schizophrenia (COATS)

Primary Purpose

Schizophrenia

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Olanzapine
Perphenazine
Aripiprazole
Metformin
Simvastatin
Benztropine
Sponsored by
National Institute of Mental Health (NIMH)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring Schizoaffective Disorder

Eligibility Criteria

18 Years - 40 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of schizophrenia or schizoaffective disorder, as defined by DSM-IV-TR criteria and confirmed by the Structured Clinical Interview for DSM-IV (SCID)
  • Treated with antipsychotic medication for less than 5 years
  • Adequate decisional capacity to make a choice about participating in this research study. Adequate decisional capacity will be determined through the aid of a 10-item decisional capacity quiz adapted from the University of California, San Diego, Brief Assessment of Capacity to Consent (UBACC) scale.
  • Psychotic exacerbation within the month prior to study entry that required psychiatric hospitalization or an increased level of care
  • Willing to use an adequate method of contraception to avoid pregnancy throughout the study and for up to 4 weeks after the study. Acceptable methods include oral, injectable, or implanted contraceptives; intrauterine devices; or barrier methods, such as condoms, diaphragm, and spermicides.

Exclusion Criteria:

  • Body mass index at or above 35 kg/m2 or below 18 kg/m2
  • Hemoglobin A1c level at or above 7%
  • Hematocrit level at or above 31%
  • Non-high density lipoprotein cholesterol at or above 190 mg/dL
  • Triglycerides at or above 500 mg/dL
  • Documented failure, defined as inefficacy or intolerability, with an adequate trial of olanzapine, perphenazine, or aripiprazole. Adequate trials last at least 4 weeks at a minimum dose of 15 mg/day of aripiprazole, 15 mg/day of olanzapine, or 16 mg/day of perphenazine.
  • Current treatment with olanzapine, perphenazine, or aripiprazole for more than 1 month
  • Known hypersensitivity to metformin, simvastatin, or benztropine
  • Treatment with a medication prescribed for weight loss
  • Diagnosis of diabetes mellitus or treatment with insulin or other diabetes medication
  • Contraindications to metformin use, including any of the following:

    • Diagnosis of congestive heart failure
    • Renal impairment, defined as serum creatinine at or above 1.5 in males and 1.4 in females, or creatinine estimated glomerular filtration rate (GFR) outside of normal limits
    • Hepatic disease, defined as aspartate transaminase (AST), alanine transaminase (ALT), or c-glutamyl transferase (CGT) more than 1.5 times upper limit of normal (ULN) or total bilirubin more than 1.2 times ULN
    • Metabolic acidosis, defined as a serum CO2 level less than the lower limit of normal
    • Recent (in the past 30 days) or scheduled radiological studies involving iodinated contrast material
    • Alcohol abuse or dependence, as determined by SCID within the past month
    • Concurrent treatment with certain drugs known to increase metformin blood levels
  • Any unstable or serious medical condition, as judged by the investigator
  • Pregnant or breastfeeding
  • Diagnosis of mental retardation or delirium, as defined by the DSM-IV-TR

Sites / Locations

  • SHANTI Clinical Trials
  • Stanford University
  • Yale University
  • University of Miami School of Medicine
  • Medical College of Georgia
  • Clinical Insights
  • University of Massachusetts
  • Wayne State University
  • University of Minnesota School of Medicine
  • Research Foundation for Mental Hygiene
  • Duke University Medical Center-John Umstead Hospital
  • University of Texas Southwestern Medical Center
  • Baylor College of Medicine

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Olanzapine

Perphenazine

Aripiprazole

Arm Description

Participants will receive treatment with olanzapine and metformin, with the possible addition of simvastatin or benztropine, depending on side effects.

Participants will receive treatment with perphenazine and benztropine, with the possible addition of simvastatin or metformin, depending on side effects.

Participants will receive treatment with aripiprazole, with the possible addition of simvastatin, metformin, or benztropine, depending on side effects.

Outcomes

Primary Outcome Measures

Feasibility of Randomizing a Cohort of Participants Meeting the Inclusion and Exclusion Criteria of the Study
Goal was to randomize 60 participants who met eligibility criteria.

Secondary Outcome Measures

Antipsychotic Efficacy, Defined as Completion of the Trial Without Psychiatric Hospitalization, Clinician Decision to Discontinue Treatment, or Patient Decision to Discontinue Treatment

Full Information

First Posted
December 3, 2008
Last Updated
January 3, 2013
Sponsor
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT00802100
Brief Title
Comparison of Optimal Antipsychotic Treatments for Adults With Schizophrenia
Acronym
COATS
Official Title
Comparison of Optimal Antipsychotic Treatments for Schizophrenia Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2012
Overall Recruitment Status
Completed
Study Start Date
December 2008 (undefined)
Primary Completion Date
September 2009 (Actual)
Study Completion Date
October 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Mental Health (NIMH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will compare the safety and effectiveness of three different antipsychotic medications, as well as the use of other medications to limit treatment side effects, in adults with schizophrenia.
Detailed Description
Schizophrenia is a chronic brain disease affecting approximately 1% of Americans. Antipsychotic medications can treat some of the most severe symptoms of schizophrenia, but they are not a cure, are often taken for long periods of time, and can have severe side effects. Other, secondary medications can provide relief from some of the most common severe side effects. This study will compare the safety and effectiveness of three different antipsychotic medications, as well as the use of additional medications to limit treatment side effects, in adults with schizophrenia. Participation in this study will last 28 to 30 weeks and include 11 visits to a study clinic. Each visit will last 2 to 3 hours. The first 2 visits will include screening and baseline measurements. The screening visit will take place at study entry, and the baseline visit will take place 3 to 14 days later. Study visits will then occur 1, 2, and 4 weeks after the baseline visit, followed by monthly visits. At the baseline visit participants will be randomly assigned to receive olanzapine, perphenazine, or aripiprazole for 28 weeks. Dosage for all three antipsychotic medications will start at low levels and be increased to full strength over 2 weeks. If participants are taking another antipsychotic when they enter the study, this 2-week period will also be used to slowly reduce and then end treatment with the non-study antipsychotic. Side effects to all three antipsychotics will be monitored, and, depending on the side effect, one of three different medications will be added to the treatment regimen. If increased cholesterol levels are experienced with any antipsychotic, simvastatin will be added; if weight gain is experienced, metformin will be added; if involuntary movements, inner restlessness, or muscle stiffness are experienced, benztropine will be added. Because of already known side effects, participants assigned to olanzapine or perphenazine will automatically add metformin or benztropine, respectively, to their regimens. Starting on the third study visit, participants will also undergo a behavioral treatment aimed at reducing cardiovascular risk factors. This behavioral treatment will involve nine 20-minute sessions, with phone calls being made to participants between sessions. During each study visit, assessments will be made of schizophrenia symptoms, side effects, adherence to medication regimen, vital signs, waist circumference, and weight. Participants will also complete a questionnaire on use of health care services and undergo instructions on exercise and eating right. On visits 1, 5, 7, and 11, blood will be drawn for standard lab tests. Additional measures at the screening visit will include questions about medical and psychiatric history, a urine test for drugs, and a questionnaire about physical and social activities.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia
Keywords
Schizoaffective Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
21 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Olanzapine
Arm Type
Experimental
Arm Description
Participants will receive treatment with olanzapine and metformin, with the possible addition of simvastatin or benztropine, depending on side effects.
Arm Title
Perphenazine
Arm Type
Experimental
Arm Description
Participants will receive treatment with perphenazine and benztropine, with the possible addition of simvastatin or metformin, depending on side effects.
Arm Title
Aripiprazole
Arm Type
Experimental
Arm Description
Participants will receive treatment with aripiprazole, with the possible addition of simvastatin, metformin, or benztropine, depending on side effects.
Intervention Type
Drug
Intervention Name(s)
Olanzapine
Other Intervention Name(s)
Zyprexa
Intervention Description
Daily tablets of 10 to 30 mg
Intervention Type
Drug
Intervention Name(s)
Perphenazine
Other Intervention Name(s)
Trilafon
Intervention Description
Daily tablets of 8 to 24 mg
Intervention Type
Drug
Intervention Name(s)
Aripiprazole
Other Intervention Name(s)
Abilify
Intervention Description
Daily tablets of 10 to 30 mg
Intervention Type
Drug
Intervention Name(s)
Metformin
Other Intervention Name(s)
Glucophage
Intervention Description
Daily tablets of 850 to 2550 mg
Intervention Type
Drug
Intervention Name(s)
Simvastatin
Other Intervention Name(s)
Zocor
Intervention Description
Daily tablets of 20 to 40 mg
Intervention Type
Drug
Intervention Name(s)
Benztropine
Other Intervention Name(s)
Cogentin
Intervention Description
Daily tablets of 1 to 2 mg
Primary Outcome Measure Information:
Title
Feasibility of Randomizing a Cohort of Participants Meeting the Inclusion and Exclusion Criteria of the Study
Description
Goal was to randomize 60 participants who met eligibility criteria.
Time Frame
Baseline
Secondary Outcome Measure Information:
Title
Antipsychotic Efficacy, Defined as Completion of the Trial Without Psychiatric Hospitalization, Clinician Decision to Discontinue Treatment, or Patient Decision to Discontinue Treatment
Time Frame
Measured over 28 weeks of study visits

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of schizophrenia or schizoaffective disorder, as defined by DSM-IV-TR criteria and confirmed by the Structured Clinical Interview for DSM-IV (SCID) Treated with antipsychotic medication for less than 5 years Adequate decisional capacity to make a choice about participating in this research study. Adequate decisional capacity will be determined through the aid of a 10-item decisional capacity quiz adapted from the University of California, San Diego, Brief Assessment of Capacity to Consent (UBACC) scale. Psychotic exacerbation within the month prior to study entry that required psychiatric hospitalization or an increased level of care Willing to use an adequate method of contraception to avoid pregnancy throughout the study and for up to 4 weeks after the study. Acceptable methods include oral, injectable, or implanted contraceptives; intrauterine devices; or barrier methods, such as condoms, diaphragm, and spermicides. Exclusion Criteria: Body mass index at or above 35 kg/m2 or below 18 kg/m2 Hemoglobin A1c level at or above 7% Hematocrit level at or above 31% Non-high density lipoprotein cholesterol at or above 190 mg/dL Triglycerides at or above 500 mg/dL Documented failure, defined as inefficacy or intolerability, with an adequate trial of olanzapine, perphenazine, or aripiprazole. Adequate trials last at least 4 weeks at a minimum dose of 15 mg/day of aripiprazole, 15 mg/day of olanzapine, or 16 mg/day of perphenazine. Current treatment with olanzapine, perphenazine, or aripiprazole for more than 1 month Known hypersensitivity to metformin, simvastatin, or benztropine Treatment with a medication prescribed for weight loss Diagnosis of diabetes mellitus or treatment with insulin or other diabetes medication Contraindications to metformin use, including any of the following: Diagnosis of congestive heart failure Renal impairment, defined as serum creatinine at or above 1.5 in males and 1.4 in females, or creatinine estimated glomerular filtration rate (GFR) outside of normal limits Hepatic disease, defined as aspartate transaminase (AST), alanine transaminase (ALT), or c-glutamyl transferase (CGT) more than 1.5 times upper limit of normal (ULN) or total bilirubin more than 1.2 times ULN Metabolic acidosis, defined as a serum CO2 level less than the lower limit of normal Recent (in the past 30 days) or scheduled radiological studies involving iodinated contrast material Alcohol abuse or dependence, as determined by SCID within the past month Concurrent treatment with certain drugs known to increase metformin blood levels Any unstable or serious medical condition, as judged by the investigator Pregnant or breastfeeding Diagnosis of mental retardation or delirium, as defined by the DSM-IV-TR
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marvin Swartz, MD
Organizational Affiliation
Duke University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
T. Scott Stroup, MD, MPH
Organizational Affiliation
University of North Carolina, Chapel Hill
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Joseph P. McEvoy, MD
Organizational Affiliation
Duke University
Official's Role
Principal Investigator
Facility Information:
Facility Name
SHANTI Clinical Trials
City
Colton
State/Province
California
ZIP/Postal Code
92324
Country
United States
Facility Name
Stanford University
City
Palo Alto
State/Province
California
ZIP/Postal Code
94305
Country
United States
Facility Name
Yale University
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06519
Country
United States
Facility Name
University of Miami School of Medicine
City
Miami
State/Province
Florida
ZIP/Postal Code
33316
Country
United States
Facility Name
Medical College of Georgia
City
Augusta
State/Province
Georgia
ZIP/Postal Code
30912
Country
United States
Facility Name
Clinical Insights
City
Glen Burnie
State/Province
Maryland
ZIP/Postal Code
21061
Country
United States
Facility Name
University of Massachusetts
City
Worcester
State/Province
Massachusetts
ZIP/Postal Code
01605
Country
United States
Facility Name
Wayne State University
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States
Facility Name
University of Minnesota School of Medicine
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55454
Country
United States
Facility Name
Research Foundation for Mental Hygiene
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Facility Name
Duke University Medical Center-John Umstead Hospital
City
Butner
State/Province
North Carolina
ZIP/Postal Code
27509
Country
United States
Facility Name
University of Texas Southwestern Medical Center
City
Dallas
State/Province
Texas
ZIP/Postal Code
75235
Country
United States
Facility Name
Baylor College of Medicine
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Comparison of Optimal Antipsychotic Treatments for Adults With Schizophrenia

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