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| 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 |
| Study Type: | Observational |
| Study Design: | Case Control, Prospective |
| Official Title: | An fMRI Study of Self-Regulation in Patients With Bulimia Nervosa |
| 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
|
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 |
Women with bulimia nervosa and age, gender, and weight-matched controls
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Contact: Amanda J. Brown, BA | 212-543-5151 | edru@pi.cpmc.columbia.edu |
| Contact: Kara Graziano, MA | 212-543-6287 | graziank@childpsych.columbia.edu |
| United States, New York | |||||
| New York State Psychiatric Institute at Columbia University Medical Center | Recruiting | ||||
| New York, New York, United States, 10032 | |||||
| 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 |
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