DLW: Effects of Antipsychotic Medications on Energy Intake and Expenditure

Sponsor
Washington University School of Medicine (Other)
Overall Status
Completed
CT.gov ID
NCT00836251
Collaborator
(none)
15
1
26
0.6

Study Details

Study Description

Brief Summary

Aim 1: To evaluate the effect of antipsychotic treatment group on Activity Energy Expenditure. The project hypothesizes that subjects treated with olanzapine will demonstrate a greater decrease in AEE over time than subjects treated with ziprasidone, due at least in part to sedating effects of olanzapine.

Aim 2: To evaluate the effect of antipsychotic treatment group on Energy Intake. The project hypothesizes that subjects treated with olanzapine will demonstrate a greater increase in EI over time than subjects treated with ziprasidone, based on higher histamine type 1 (H1) receptor affinity of olanzapine and the relationship between H1 affinity and hunger and/or satiety.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: H218O and 2H2O, administered as a mixed cocktail

Detailed Description

The overall purpose of this research is to determine how two commonly prescribed antipsychotic medications, olanzapine (Zyprexa) and ziprasidone (Geodon), affect weight gain through increasing appetite and/or through increasing sedation that results in decreased activity.

Undesirable changes in body weight, blood sugar control, type 2 diabetes, and blood lipids occur more commonly in people who have schizophrenia than in people without psychiatric conditions. Although differences in glucose regulation were first reported in schizophrenia before the use of antipsychotic medications, antipsychotic treatment may contribute to these problems, though just how this happens is not understood. This study proposes to use a doubly-labeled water (DLW) method to measure the degree to which weight gain (fat mass) is due to increased appetite, decreased physical activity from being tired and sleepy, or some combination of both. Doubly-labeled water contains stable isotopes (non-radioactive forms) of the hydrogen and oxygen that make up all water, isotopes that will be slowly passed out through the urine after participants drink DLW. The number of hydrogen and oxygen isotopes found in the urine samples will tell us how many calories the participant's body has been using.

The DLW method has been used in people with obesity and other types of medical problems. It's recognized as the most accurate measure of the number of calories burned throughout a typical day, and how many calories are taken in from food and drink. By measuring these factors in people who take antipsychotic medications, doctors will gain a better understanding of the effects of antipsychotic medications on body weight and fat mass. This could lead to the development of better ways to prevent or treat weight gain or diabetes in patients who take antipsychotic medications.

Study Design

Study Type:
Observational
Actual Enrollment :
15 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Effects of Antipsychotic Medications on Energy Intake and Expenditure
Study Start Date :
Apr 1, 2006
Actual Primary Completion Date :
Jun 1, 2008
Actual Study Completion Date :
Jun 1, 2008

Arms and Interventions

Arm Intervention/Treatment
H218O and 2H2O

schizophrenia

Dietary Supplement: H218O and 2H2O, administered as a mixed cocktail
0.195 g of H218O and 0.117 g of 2H2O per kg of estimated total body water (TBW), administered as a mixed cocktail

Outcome Measures

Primary Outcome Measures

  1. treatment-induced changes in Total Energy Expenditure (TEE), Activity Energy Expenditure (AEE), and Energy Intake (EI) [12 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • non-diabetic

  • schizophrenic or schizoaffective

  • currently prescribed olanzapine or ziprasidone

  • 18-80 y.o.

Exclusion Criteria:
  • <18 or >80 years of age

  • diabetic

  • not schizophrenic or schizoaffective

  • not currently prescribed olanzapine or ziprasidone

Contacts and Locations

Locations

Site City State Country Postal Code
1 Washington University School of Medicine St. Louis Missouri United States 53110

Sponsors and Collaborators

  • Washington University School of Medicine

Investigators

  • Principal Investigator: John W Newcomer, MD, Florida Atlantic University
  • Principal Investigator: Ginger Nicol, MD, Washington University School of Medicine

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Washington University School of Medicine
ClinicalTrials.gov Identifier:
NCT00836251
Other Study ID Numbers:
  • 06-0246
First Posted:
Feb 4, 2009
Last Update Posted:
Mar 13, 2014
Last Verified:
Mar 1, 2014
Keywords provided by Washington University School of Medicine
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 13, 2014