A Comparison of Long-acting Injectable Medications for Schizophrenia (ACLAIMS)
Primary Purpose
Schizophrenia, Schizoaffective Disorder
Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
haloperidol decanoate
paliperidone palmitate
Sponsored by
About this trial
This is an interventional treatment trial for Schizophrenia
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of schizophrenia or schizoaffective disorder as defined by DSM-IV-TR criteria
- Age 18-65 years
- Capacity to provide informed consent
- Patients who are likely to benefit from treatment with long-acting injectable paliperidone palmitate or haloperidol decanoate
- Women of child bearing potential must have a negative serum pregnancy test at the Screening Visit.
Exclusion Criteria:
- Patients who are currently stable and doing well on an antipsychotic regimen
- Patients not expected to benefit from the study medications due to past experience with risperidone, paliperidone or haloperidol
- Patients with tardive dyskinesia that is moderate or severe
- Patients with any medical condition that, in the judgment of the investigator, might preclude safe completion of the study
- Women who are pregnant or breastfeeding
- Patients with mental retardation
Sites / Locations
- VA Palo Alto Heathcare Systems
- Yale University/Connecticut Mental Health Center
- University of Miami School of Medicine
- Medical College of Georgia
- University of Iowa Hospital
- Clinical Research Institute
- Clinical Insights, Inc.
- John D. Dingell VA Medical Center
- Sparrow St. Lawrence Hospital, Michigan State University Psychiatry
- Kansas City Veterans Affairs Medical Center
- Creighton University Dept. of Psychiatry
- Research Foundation for Mental Hygiene
- University of Rochester
- John Umstead Hospital/Duke University
- University of North Carolina
- Carolina Behavioral Care
- Louis Stokes Cleveland VA Medical Center
- Philadelphia VA Medical Center-116A
- University of Texas Southwestern Medical Center
- Central Texas Veterans Health Care System
- Frontier Institute
- VA Puget Sound Health Care System
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Paliperidone palmitate
Haloperidol decanoate
Arm Description
Intramuscular injections of paliperidone palmitate 39-234 mg every month
Intramuscular injections of haloperidol decanoate 25-200 mg every month
Outcomes
Primary Outcome Measures
Efficacy Failure
Efficacy failure as indicated by psychiatric hospitalization, need for crisis intervention, clinical decision that oral antipsychotic medication cannot be discontinued in less than eight weeks, a clinical decision to discontinue the medication due to inadequate benefit, or the ongoing or repeated need for adjunctive antipsychotic medication.
Secondary Outcome Measures
Changes in Psychiatric Symptoms
The Positive and Negative Syndrome Scale measures the core symptoms associated with schizophrenia. The measure includes 30 items rated from 1=absent to 7=extremely severe. Full range of scores is 30-210 with higher scores representing more severe illness. Reductions in symptoms over time represent improvement.
Full Information
NCT ID
NCT01136772
First Posted
May 14, 2010
Last Updated
September 6, 2016
Sponsor
New York State Psychiatric Institute
Collaborators
National Institute of Mental Health (NIMH), Duke University, University of North Carolina, Chapel Hill
1. Study Identification
Unique Protocol Identification Number
NCT01136772
Brief Title
A Comparison of Long-acting Injectable Medications for Schizophrenia
Acronym
ACLAIMS
Official Title
A Comparison of Long-Acting Injectable Medications for Schizophrenia
Study Type
Interventional
2. Study Status
Record Verification Date
July 2016
Overall Recruitment Status
Completed
Study Start Date
March 2011 (undefined)
Primary Completion Date
July 2013 (Actual)
Study Completion Date
July 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
New York State Psychiatric Institute
Collaborators
National Institute of Mental Health (NIMH), Duke University, University of North Carolina, Chapel Hill
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this research study is to compare the "real-world" effectiveness of two FDA-approved and widely used long-acting injectable antipsychotic medications (paliperidone palmitate and haloperidol decanoate) in patients with schizophrenia or schizoaffective disorder who are expected to benefit from the improved medication compliance associated with injectable medications. The goal is to evaluate the effects of the medications on outcomes of importance to patients (relapse, symptoms, adverse effects, functioning) as well as policy makers (all of the above plus costs).
Detailed Description
The purpose of this comparative effectiveness research study is to learn more about different medications called antipsychotics that are used to treat schizophrenia or schizoaffective disorder. Specifically, we are looking at long-acting medications that are given by injection every month, instead of being taken by mouth every day. In this multi-site study, we are comparing the risk and benefits of two FDA-approved long-acting injectable medications (paliperidone palmitate and haloperidol decanoate). Study participants with schizophrenia or schizoaffective disorder are expected to benefit from the improved medication schedule.
This study aims to enroll 360 individuals with schizophrenia or schizoaffective disorder for whom treatment with a long-acting injectable antipsychotic medication is likely to be helpful. Study participants will be randomly assigned to treatment with either paliperidone palmitate and haloperidol decanoate for up to 24 months. Participants will have an equal chance of being assigned to each medication, however participants will not know which medication they are taking.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Schizoaffective Disorder
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
311 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Paliperidone palmitate
Arm Type
Experimental
Arm Description
Intramuscular injections of paliperidone palmitate 39-234 mg every month
Arm Title
Haloperidol decanoate
Arm Type
Active Comparator
Arm Description
Intramuscular injections of haloperidol decanoate 25-200 mg every month
Intervention Type
Drug
Intervention Name(s)
haloperidol decanoate
Other Intervention Name(s)
Haldol
Intervention Description
haloperidol decanoate injections, 25-200 mg once a month
Intervention Type
Drug
Intervention Name(s)
paliperidone palmitate
Other Intervention Name(s)
Invega Sustenna
Intervention Description
Paliperidone palmitate injections, 39 mg - 234 mg once a month
Primary Outcome Measure Information:
Title
Efficacy Failure
Description
Efficacy failure as indicated by psychiatric hospitalization, need for crisis intervention, clinical decision that oral antipsychotic medication cannot be discontinued in less than eight weeks, a clinical decision to discontinue the medication due to inadequate benefit, or the ongoing or repeated need for adjunctive antipsychotic medication.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Changes in Psychiatric Symptoms
Description
The Positive and Negative Syndrome Scale measures the core symptoms associated with schizophrenia. The measure includes 30 items rated from 1=absent to 7=extremely severe. Full range of scores is 30-210 with higher scores representing more severe illness. Reductions in symptoms over time represent improvement.
Time Frame
Baseline to 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of schizophrenia or schizoaffective disorder as defined by DSM-IV-TR criteria
Age 18-65 years
Capacity to provide informed consent
Patients who are likely to benefit from treatment with long-acting injectable paliperidone palmitate or haloperidol decanoate
Women of child bearing potential must have a negative serum pregnancy test at the Screening Visit.
Exclusion Criteria:
Patients who are currently stable and doing well on an antipsychotic regimen
Patients not expected to benefit from the study medications due to past experience with risperidone, paliperidone or haloperidol
Patients with tardive dyskinesia that is moderate or severe
Patients with any medical condition that, in the judgment of the investigator, might preclude safe completion of the study
Women who are pregnant or breastfeeding
Patients with mental retardation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Scott Stroup, MD, MPH
Organizational Affiliation
Columbia University
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
VA Palo Alto Heathcare Systems
City
Palo Alto
State/Province
California
ZIP/Postal Code
94304
Country
United States
Facility Name
Yale University/Connecticut Mental Health Center
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
University of Iowa Hospital
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52242
Country
United States
Facility Name
Clinical Research Institute
City
Wichita
State/Province
Kansas
ZIP/Postal Code
67207
Country
United States
Facility Name
Clinical Insights, Inc.
City
Glen Burnie
State/Province
Maryland
ZIP/Postal Code
21061
Country
United States
Facility Name
John D. Dingell VA Medical Center
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States
Facility Name
Sparrow St. Lawrence Hospital, Michigan State University Psychiatry
City
Lansing
State/Province
Michigan
ZIP/Postal Code
48915
Country
United States
Facility Name
Kansas City Veterans Affairs Medical Center
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64128
Country
United States
Facility Name
Creighton University Dept. of Psychiatry
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68131
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
University of Rochester
City
Rochester
State/Province
New York
ZIP/Postal Code
14623
Country
United States
Facility Name
John Umstead Hospital/Duke University
City
Butner
State/Province
North Carolina
ZIP/Postal Code
27509
Country
United States
Facility Name
University of North Carolina
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599-7160
Country
United States
Facility Name
Carolina Behavioral Care
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27705
Country
United States
Facility Name
Louis Stokes Cleveland VA Medical Center
City
Brecksville
State/Province
Ohio
ZIP/Postal Code
44141
Country
United States
Facility Name
Philadelphia VA Medical Center-116A
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
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
Central Texas Veterans Health Care System
City
Waco
State/Province
Texas
ZIP/Postal Code
78711
Country
United States
Facility Name
Frontier Institute
City
Spokane
State/Province
Washington
ZIP/Postal Code
99204
Country
United States
Facility Name
VA Puget Sound Health Care System
City
Tacoma
State/Province
Washington
ZIP/Postal Code
98493
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
24846035
Citation
McEvoy JP, Byerly M, Hamer RM, Dominik R, Swartz MS, Rosenheck RA, Ray N, Lamberti JS, Buckley PF, Wilkins TM, Stroup TS. Effectiveness of paliperidone palmitate vs haloperidol decanoate for maintenance treatment of schizophrenia: a randomized clinical trial. JAMA. 2014 May 21;311(19):1978-87. doi: 10.1001/jama.2014.4310. Erratum In: JAMA. 2014 Oct 8;312(14):1473.
Results Reference
result
PubMed Identifier
27247177
Citation
Rosenheck RA, Leslie DL, Sint KJ, Lin H, Li Y, McEvoy JP, Byerly MJ, Hamer RM, Swartz MS, Stroup TS. Cost-Effectiveness of Long-Acting Injectable Paliperidone Palmitate Versus Haloperidol Decanoate in Maintenance Treatment of Schizophrenia. Psychiatr Serv. 2016 Oct 1;67(10):1124-1130. doi: 10.1176/appi.ps.201500447. Epub 2016 Jun 1.
Results Reference
result
PubMed Identifier
30549494
Citation
Stroup TS, Bareis NA, Rosenheck RA, Swartz MS, McEvoy JP. Heterogeneity of Treatment Effects of Long-Acting Injectable Antipsychotic Medications. J Clin Psychiatry. 2018 Nov 27;80(1):18m12109. doi: 10.4088/JCP.18m12109.
Results Reference
derived
Learn more about this trial
A Comparison of Long-acting Injectable Medications for Schizophrenia
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