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Brain Function of Self-Regulation in Women With Bulimia Nervosa

This study is currently recruiting participants.
Verified by National Institute of Mental Health (NIMH), March 2008

Sponsored by: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)
ClinicalTrials.gov Identifier: NCT00345943
  Purpose

This study will compare brain images of females with bulimia and females without eating disorders to better understand the brain's involvement with self-regulation.


Condition Intervention
Eating Disorders
Procedure: fMRI
Procedure: Neuropsychological Testing

MedlinePlus related topics:   Eating Disorders    MRI Scans   

U.S. FDA Resources

Study Type:   Observational
Study Design:   Case Control, Prospective
Official Title:   An fMRI Study of Self-Regulation in Patients With Bulimia Nervosa

Further study details as provided by National Institute of Mental Health (NIMH):

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment:   80
Study Start Date:   November 2004

Groups/Cohorts Assigned Interventions
1
Women with bulimia nervosa
Procedure: fMRI
Functional Magnetic Resonance Imaging scans
Procedure: Neuropsychological Testing
Neuropsychological tests
2
Healthy control subjects
Procedure: fMRI
Functional Magnetic Resonance Imaging scans
Procedure: Neuropsychological Testing
Neuropsychological tests

Detailed Description:

Bulimia nervosa, also called bulimia, is an eating disorder that is characterized by episodes of binge eating followed by inappropriate methods of weight control, such as vomiting, fasting, and the excessive use of laxatives. Research has shown that individuals with bulimia may have difficulties with self-regulation, which is the ability to make independent decisions and exercise judgment and control over behavior. Self-regulation dysfunction may be evident on brain scans as abnormal brain activity. This study will use functional magnetic resonance imaging (fMRI) to compare women with bulimia to women without eating disorders in terms of how their brain processes self-regulation.

This study will enroll women with bulimia, as well as women with no history of eating disorders. Participants will attend an initial 2- to 3-hour screening visit at which time their vital signs, height, and weight will be recorded. Standardized questionnaires regarding current and past bulimia symptoms will be completed, and a study physician may review the questionnaires with participants. Participants will have the option of completing neuropsychological tests and an fMRI scan either at the time of the screening visit or at a later date. The neuropsychological tests will take approximately 3 hours to complete, and will include puzzles, simple computer tests, and tests on coordination, concentration, and memory. The fMRI scan will also take approximately 3 hours. During the scan, participants may be asked to perform various tasks, such as pushing a button or watching a television screen.

  Eligibility
Ages Eligible for Study:   18 Years to 60 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample

Study Population

Women with bulimia nervosa and age, gender, and weight-matched controls


Criteria

Inclusion Criteria:

  • Current or prior diagnosis of bulimia nervosa
  • For control group participants, no current or past history of an eating disorder

Exclusion Criteria:

  • Ferromagnetic implants (e.g., pacemaker)
  • Metal braces or retainers
  • IQ less than 80
  • Any other current major Axis I disorder, other than obsessive-compulsive disorder (OCD) or major depressive disorder (MDD)
  • History of concussion, seizure disorder, or other neurological illness
  • Claustrophobia
  • Pregnant
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00345943

Contacts
Contact: Amanda J. Brown, BA     212-543-5151     edru@pi.cpmc.columbia.edu    
Contact: Kara Graziano, MA     212-543-6287     graziank@childpsych.columbia.edu    

Locations
United States, New York
New York State Psychiatric Institute at Columbia University Medical Center     Recruiting
      New York, New York, United States, 10032

Sponsors and Collaborators

Investigators
Principal Investigator:     Rachel Marsh, PhD     Columbia University    
  More Information

Responsible Party:   The New York State Psychiatric Institute ( Joanna Steinglass, MD )
Study ID Numbers:   K01 MH77652, DDTR BK-TKAR
First Received:   June 28, 2006
Last Updated:   March 28, 2008
ClinicalTrials.gov Identifier:   NCT00345943
Health Authority:   United States: Federal Government

Keywords provided by National Institute of Mental Health (NIMH):
Bulimia Nervosa  
Bulimia  
fMRI  
Magnetic Resonance Imaging  

Study placed in the following topic categories:
Signs and Symptoms
Bulimia Nervosa
Signs and Symptoms, Digestive
Mental Disorders
Bulimia
Eating Disorders
Hyperphagia

ClinicalTrials.gov processed this record on August 08, 2008




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