ADAPT: Effect of Antipsychotics on Appetite Regulation

Sponsor
University of North Carolina, Chapel Hill (Other)
Overall Status
Completed
CT.gov ID
NCT00903916
Collaborator
National Institute of Mental Health (NIMH) (NIH)
45
1
55
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Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate changes in appetite-regulating hormones, body composition (weight, body fat%), and hunger ratings in persons early in treatment with one of four atypical antipsychotic medications (olanzapine, risperidone, ziprasidone, aripiprazole).

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Severe weight gain and glucose dysregulation are serious problems in patients treated with second-generation ('atypical') antipsychotics (SGA). These side effects frequently interfere with medication compliance and necessitate discontinuation of treatment. Although the causal mechanisms for weight and glucose dysregulation are not well understood, one promising area of investigation targets SGA-induced disturbances in appetite and in appetite-regulating hormones. Findings from our group (and others) demonstrate SGA treatment-related increases in fasting levels of the appetite-stimulating hormone, ghrelin, as well as increases in self-report hunger. This novel study will examine prospective changes in ghrelin and in the 'satiety-signaling' peptide YY (PYY) as measured before and after participants consume a standard mixed-macronutrient meal. Data are obtained at baseline (within 4 weeks of beginning medication), and again 2 months and 4 months later.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    45 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    Effect of Weight-increasing Psychotropic Medications on Appetite Regulation
    Study Start Date :
    Aug 1, 2007
    Actual Primary Completion Date :
    Mar 1, 2012
    Actual Study Completion Date :
    Mar 1, 2012

    Outcome Measures

    Primary Outcome Measures

    1. ghrelin area under the curve [baseline, 2 and 4 months]

    2. PYY area under the curve [baseline, 2 and 4 months]

    Secondary Outcome Measures

    1. glucose area under the curve [baseline, 2 and 4 months]

    2. insulin area under the curve [baseline, 2 and 4 months]

    3. body composition [baseline, 2 and 4 months]

    4. subjective appetite ratings [baseline, 2 and 4 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 40 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Meets DSM IV criteria for a psychotic disorder (schizophrenia, schizophreniform, brief psychotic disorder, schizoaffective disorder), bipolar disorder, or major depression with psychotic features;

    2. "Drug naïve" prior to most recent psychiatric diagnosis;

    3. Currently prescribed one of four atypical antipsychotic medications: olanzapine, risperidone, ziprasidone, or aripiprazole;

    4. Between the ages of 18 and 40, any race and either gender;

    5. Not obese (BMI < 30 kg/m2) (fasting and postprandial ghrelin levels are altered in obesity);

    6. Has negative histories for cardiovascular, metabolic, and endocrine disorders at screening;

    7. Is willing and able to eat animal-derived foods; and

    8. Is not exercising 3 or more times per week.

    Exclusion Criteria:
    1. Use of medications to treat metabolic and endocrine abnormalities, corticosteroids, over-the-counter appetite suppressants that contain phentermine or Sibutramine;

    2. Active involvement with a weight loss program (i.e., Weight Watchers);

    3. Serious or unstable medical illness which requires ongoing treatment with medication (this does not include hypertension);

    4. Anemia;

    5. At serious suicidal risk;

    6. Current substance abuse or dependence;

    7. For female subjects, pregnancy or nursing (because pregnancy may influence appetite and because the body composition procedure involves low level X-ray exposure).

    8. Known history of mental retardation or dementia.

    9. Children and adolescents under age 18 will be excluded owing to the inherent confounding effects of normal growth on body weight and appetite.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of North Carolina at Chapel Hill Chapel Hill North Carolina United States 27599

    Sponsors and Collaborators

    • University of North Carolina, Chapel Hill
    • National Institute of Mental Health (NIMH)

    Investigators

    • Principal Investigator: Kimberly A Brownley, PhD, University of North Carolina, Chapel Hill

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Kimberly Brownley, Assistant Professor, University of North Carolina, Chapel Hill
    ClinicalTrials.gov Identifier:
    NCT00903916
    Other Study ID Numbers:
    • 3024-04003
    • 1R01MH077117-01A2
    First Posted:
    May 19, 2009
    Last Update Posted:
    Apr 3, 2012
    Last Verified:
    Apr 1, 2012
    Keywords provided by Kimberly Brownley, Assistant Professor, University of North Carolina, Chapel Hill
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 3, 2012