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Evaluating the Brain's Response to Natural Versus Artificial Sweetener in Women Who Have Had an Eating Disorder
This study has been completed.
Study NCT00517335   Information provided by National Institute of Mental Health (NIMH)
First Received: August 14, 2007   Last Updated: March 26, 2008   History of Changes

August 14, 2007
March 26, 2008
May 2005
January 2008   (final data collection date for primary outcome measure)
 
 
Complete list of historical versions of study NCT00517335 on ClinicalTrials.gov Archive Site
 
 
 
Evaluating the Brain's Response to Natural Versus Artificial Sweetener in Women Who Have Had an Eating Disorder
The Evaluation of Brain Neuronal Activity in Response to Natural (Sucrose) and Artificial (Sucralose) Taste Stimuli- Does Caloric Content Matter to the Brain?

This study will compare the brain's ability to distinguish between natural and artificial sweeteners in women with and without a history of eating disorders.

Eating disorders often result in serious illness and can lead to prolonged health complications, including heart and kidney problems, digestive disorders, nerve damage, and low blood pressure. Anorexia nervosa and bulimia nervosa are examples eating disorders. People with anorexia nervosa do not eat enough in fear of becoming overweight, resulting in extreme weight loss. People with bulimia nervosa first binge by consuming hundreds or even thousands of calories within a very short time period and then purge by either vomiting or using laxatives. Women are at a greater risk of developing the disorders, particularly when they are between the ages of 12 and 24. Treatments for eating disorders typically include nutrition counseling, psychotherapy, and medication. To better understand eating disorders, this study will compare the brain's ability to distinguish between natural and artificial sweeteners in women with and without a history of eating disorders.

All participants in this observational study will be administered a taste test to determine if they can consciously differentiate between a sugar solution and an artificially sweetened solution. Participants may also perform several brief computerized tests, ranging from 3 to 10 minutes each, to evaluate thinking, memory, and information processing skills. Participants who cannot tell the difference between the solutions will undergo a functional magnetic resonance imaging (fMRI) scan, which will take pictures of the brain and blood flowing through the brain. Prior to the scan, blood and urine collection may occur, and participants may complete two additional computerized tests. The scan will require 60 to 90 minutes to complete. During the scan, participants will hold two thin tubes in their mouth. At various intervals, these tubes will deliver 1 ml of liquid containing either sugar water or an artificial sweetener into each participant's mouth. A screen projection of abstract pictures will also be shown to each participant throughout the scan, either before the liquid is delivered or alone. This study will require a 6- to 9-hour time commitment. The results from this study may provide valuable information regarding anorexia nervosa and bulimia nervosa and may eventually lead to the development of new and better treatment options for these complex and serious disorders.

 
Observational
Case Control, Prospective
Eating Disorders
Procedure: Functional magnetic resonance imaging (fMRI) scan
  • Women who are healthy controls
  • Women who have recovered from bulimia
  • Women who have recovered from anorexia
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
60
January 2008
January 2008   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Right-handed
  • Recovered from anorexia or bulimia nervosa at least 12 months prior to study entry
  • Met DSM criteria for anorexia or bulimia nervosa at one time within 3 years prior to study entry

Exclusion Criteria:

  • Pregnant or breastfeeding
  • Currently taking any medication (except birth control)
  • Any current mental illness
  • Any metal in body
Female
18 Years to 45 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00517335
Walter Kaye, MD Professor of Psychiatry, University of California San Diego
R01 MH46001, DATR A3-NSS
National Institute of Mental Health (NIMH)
 
Principal Investigator: Watler Kaye, MD University of California, San Diego (UCSD)
National Institute of Mental Health (NIMH)
March 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP