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Improving Metabolic Parameters of Antipsychotic Child Treatment With Ziprasidone, Aripiprazole, and Clozapine (ZAC)

Primary Purpose

Weight Gain

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
metformin
healthy lifestyle intervention
Sponsored by
University of North Carolina, Chapel Hill
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Weight Gain focused on measuring antipsychotic, metformin, children, adolescents

Eligibility Criteria

10 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Ages 10 to 17 years (inclusive).
  • Receiving treatment with ziprasidone, aripiprazole or clozapine for the past 56 days or longer.
  • Clinically stable on current treatment regimen (see Rationales below).
  • Stable dose of current psychotropic co-medications for at least 30 days.
  • BMI increase of > 7% within 3 months OR a > 0.5 BMI z-score increase within the past 24 months while taking olanzapine, quetiapine or risperidone, with maintenance of the threshold level of weight gain.
  • Lifetime diagnosis of a schizophrenia spectrum disorder (schizophrenia, schizoaffective disorder, psychotic disorder NOS), a bipolar spectrum disorder (bipolar disorder, bipolar disorder NOS), certain mood disorders (mood disorder NOS, major depressive disorder with psychotic features), or certain disruptive/aggressive disorders (conduct disorder, intermittent explosive disorder, autism spectrum disorder with history of clinically significant levels of disruptive behaviors as defined below) using DSM-IV criteria determined by clinical interview and K-SADS-PL.
  • Sexually active girls must agree to use an effective form of birth control or be abstinent.
  • Principle caretaker is able to participate in study appointments as is clinically indicated.
  • guardian and the child must agree (legally consent and assent) to participation.

Exclusion Criteria:

  • Any medication that would significantly alter glucose, insulin or lipid levels. Prohibited medications will include, but are not limited to: insulin, steroids, topiramate, sibutramine, orlistat, metformin, amantadine, vitamin E (other than in standard multivitamins), antidiabetic drugs, HIV drugs.
  • Major neurological disorder or medical illness that affects weight gain (e.g., unstable thyroid disease), requires a prohibited systemic medication or procedure (e.g., diabetes mellitus [insulin], chronic renal failure [steroids]) or that would prevent participation in physical activity in the healthy lifestyle program.
  • Current active thyroid (TSH >18 microIU/ml), hepatic (2 LFTs >4x upper limits of normal), renal (serum Creatinine >1.4 mg/dL in females and serum Creatinine >1.5 mg/dL in males), cardiac, gastrointestinal, or adrenal disease.
  • Fasting glucose > 125 mg/dL on two occasions indicating need for prompt treatment for diabetes.
  • Child meets DSM-IV criteria for substance abuse or dependence disorder within the past month, not including tobacco abuse or dependence • Current treatment with more than one antipsychotic medication.
  • Current treatment with more than 5 total psychotropic medications (i.e., 4 psychotropics plus SGA).
  • Known hypersensitivity to metformin.
  • Pregnant or breast feeding.
  • Current or lifetime diagnosis of anorexia nervosa or bulimia nervosa.
  • Significant risk for dangerousness to self or to others that makes participating inadvisable.
  • Language issues that prevent child and/or parent from completing assessments or treatment.
  • Ongoing or previously undisclosed child abuse requiring new department of social service intervention.

Sites / Locations

  • University of North Carolina, Department of Psychiatry

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

1

2

3

Arm Description

metformin, 250mg-2000 mg/day, in BID to TID doses for 26 weeks. Open, flexibly adjusted.

Healthy lifestyle intervention. Additional meeting at each psychiatric visit to review weight changes, level of physical activity and healthy eating behaviors

Self-selected patients will be followed at major timepoints to assess weight and related measures.

Outcomes

Primary Outcome Measures

Percent Change in BMI
Absolute Change in Weight
Percent Change in Fat Mass
Percent Change in Weight

Secondary Outcome Measures

Percent Change in Insulin Levels
Percent Change in Total Cholesterol
Percent Change in Triglycerides
Incidence of Metabolic Syndrome
Percent Change in Glucose Levels
Percent Change in HDL
Percent Change in LDL

Full Information

First Posted
February 5, 2008
Last Updated
November 28, 2012
Sponsor
University of North Carolina, Chapel Hill
Collaborators
Foundation of Hope, North Carolina
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1. Study Identification

Unique Protocol Identification Number
NCT00617058
Brief Title
Improving Metabolic Parameters of Antipsychotic Child Treatment With Ziprasidone, Aripiprazole, and Clozapine
Acronym
ZAC
Official Title
Improving Metabolic Parameters of Antipsychotic Child Treatment With Ziprasidone, Aripiprazole, and Clozapine
Study Type
Interventional

2. Study Status

Record Verification Date
November 2012
Overall Recruitment Status
Terminated
Why Stopped
Terminated in lieu of similar,competing large, multi-site study.
Study Start Date
March 2007 (undefined)
Primary Completion Date
June 2010 (Actual)
Study Completion Date
September 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of North Carolina, Chapel Hill
Collaborators
Foundation of Hope, North Carolina

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate the relative risks and benefits of two approaches to the control of weight gain and other negative side effects in children and adolescents on 2nd generation antipsychotics (SGA): Healthy lifestyle instruction (nutritional and physical activity surveillance and advice) + continuation of current SGA; Add the diabetes drug, metformin + continuation of current SGA.
Detailed Description
The proposed pilot study is being conducted to obtain pilot data to support a grant application for a multi-site randomized controlled trial. The primary objective is to evaluate the relative risks and benefits of two approaches to the control of weight gain and other negative side effects in children and adolescents on 2nd generation antipsychotics (SGA). The critical question being addressed is: What can be done for the many youth who have gained substantial weight or developed high levels of lipids or glucose in their blood on an SGA; but due to their illness require continued treatment with an antipsychotic? At least 40 youths (and no more than 60) age 10-17 that have gained substantial weight while taking a frequently used SGA: ziprasidone, aripiprazole or clozapine will be randomized to one of two treatments for 6 months: Healthy lifestyle instruction (nutritional and physical activity surveillance and advice) + continuation of current SGA; Add the diabetes drug, metformin + continuation of current SGA. Subjects may also elect to be in an observational arm that involves no intervention but the same major assessments. Height, weight, body fat, and various blood tests indicative of general health will be collected during the 6 month trial to monitor the health benefits and safety of the interventions. SGAs are associated with concerning degrees of weight gain and metabolic consequences. Children and adolescents, in whom SGAs are used increasingly for a wide variety of conditions, are particularly vulnerable to these side effects, which adversely affect health and longevity. It is imperative that researchers evaluate the efficacy and safety of interventions designed to prevent and treat the weight gain and metabolic problems caused by antipsychotic treatment of children. Lifestyle interventions and adjunctive medications all hold some promise of efficacy. However, it is essential that these strategies be rigorously evaluated as soon as possible in order to prevent the ongoing health consequences of SGA treatment in another generation of children with serious psychiatric illnesses.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Weight Gain
Keywords
antipsychotic, metformin, children, adolescents

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
metformin, 250mg-2000 mg/day, in BID to TID doses for 26 weeks. Open, flexibly adjusted.
Arm Title
2
Arm Type
Experimental
Arm Description
Healthy lifestyle intervention. Additional meeting at each psychiatric visit to review weight changes, level of physical activity and healthy eating behaviors
Arm Title
3
Arm Type
No Intervention
Arm Description
Self-selected patients will be followed at major timepoints to assess weight and related measures.
Intervention Type
Drug
Intervention Name(s)
metformin
Other Intervention Name(s)
Glucophage
Intervention Description
open dosed, randomly assigned flexible dose treatment with 250-2000mg/day divided BID or TID
Intervention Type
Behavioral
Intervention Name(s)
healthy lifestyle intervention
Intervention Description
additional component to regular psychiatric visits that includes monitoring of lifestyle and eating behaviors.
Primary Outcome Measure Information:
Title
Percent Change in BMI
Time Frame
24 weeks
Title
Absolute Change in Weight
Time Frame
24 weeks
Title
Percent Change in Fat Mass
Time Frame
24 weeks
Title
Percent Change in Weight
Time Frame
24 weeks
Secondary Outcome Measure Information:
Title
Percent Change in Insulin Levels
Time Frame
24 weeks
Title
Percent Change in Total Cholesterol
Time Frame
24 weeks
Title
Percent Change in Triglycerides
Time Frame
24 weeks
Title
Incidence of Metabolic Syndrome
Time Frame
24 weeks
Title
Percent Change in Glucose Levels
Time Frame
24 weeks
Title
Percent Change in HDL
Time Frame
24 weeks
Title
Percent Change in LDL
Time Frame
24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ages 10 to 17 years (inclusive). Receiving treatment with ziprasidone, aripiprazole or clozapine for the past 56 days or longer. Clinically stable on current treatment regimen (see Rationales below). Stable dose of current psychotropic co-medications for at least 30 days. BMI increase of > 7% within 3 months OR a > 0.5 BMI z-score increase within the past 24 months while taking olanzapine, quetiapine or risperidone, with maintenance of the threshold level of weight gain. Lifetime diagnosis of a schizophrenia spectrum disorder (schizophrenia, schizoaffective disorder, psychotic disorder NOS), a bipolar spectrum disorder (bipolar disorder, bipolar disorder NOS), certain mood disorders (mood disorder NOS, major depressive disorder with psychotic features), or certain disruptive/aggressive disorders (conduct disorder, intermittent explosive disorder, autism spectrum disorder with history of clinically significant levels of disruptive behaviors as defined below) using DSM-IV criteria determined by clinical interview and K-SADS-PL. Sexually active girls must agree to use an effective form of birth control or be abstinent. Principle caretaker is able to participate in study appointments as is clinically indicated. guardian and the child must agree (legally consent and assent) to participation. Exclusion Criteria: Any medication that would significantly alter glucose, insulin or lipid levels. Prohibited medications will include, but are not limited to: insulin, steroids, topiramate, sibutramine, orlistat, metformin, amantadine, vitamin E (other than in standard multivitamins), antidiabetic drugs, HIV drugs. Major neurological disorder or medical illness that affects weight gain (e.g., unstable thyroid disease), requires a prohibited systemic medication or procedure (e.g., diabetes mellitus [insulin], chronic renal failure [steroids]) or that would prevent participation in physical activity in the healthy lifestyle program. Current active thyroid (TSH >18 microIU/ml), hepatic (2 LFTs >4x upper limits of normal), renal (serum Creatinine >1.4 mg/dL in females and serum Creatinine >1.5 mg/dL in males), cardiac, gastrointestinal, or adrenal disease. Fasting glucose > 125 mg/dL on two occasions indicating need for prompt treatment for diabetes. Child meets DSM-IV criteria for substance abuse or dependence disorder within the past month, not including tobacco abuse or dependence • Current treatment with more than one antipsychotic medication. Current treatment with more than 5 total psychotropic medications (i.e., 4 psychotropics plus SGA). Known hypersensitivity to metformin. Pregnant or breast feeding. Current or lifetime diagnosis of anorexia nervosa or bulimia nervosa. Significant risk for dangerousness to self or to others that makes participating inadvisable. Language issues that prevent child and/or parent from completing assessments or treatment. Ongoing or previously undisclosed child abuse requiring new department of social service intervention.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Linmarie Sikich, MD
Organizational Affiliation
University of North Carolina, Department of Psychiatry
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of North Carolina, Department of Psychiatry
City
Chapel HIll
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States

12. IPD Sharing Statement

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Improving Metabolic Parameters of Antipsychotic Child Treatment With Ziprasidone, Aripiprazole, and Clozapine

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