Follow-Up Extension to the Family Study of Binge Eating Disorder
NCT ID: NCT00777634
Last Updated: 2012-05-29
Study Results
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View full resultsBasic Information
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COMPLETED
268 participants
OBSERVATIONAL
2005-06-30
2009-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Binge eating disorder (BED)
Individuals who meet criteria for binge eating disorder.
No intervention.
There is no intervention used in this study. Cohort members are interviewed and blood pressure, weight, and laboratory specimens are obtained.
Without BED
Individuals who do not meet criteria for binge eating disorder.
No intervention.
There is no intervention used in this study. Cohort members are interviewed and blood pressure, weight, and laboratory specimens are obtained.
Interventions
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No intervention.
There is no intervention used in this study. Cohort members are interviewed and blood pressure, weight, and laboratory specimens are obtained.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
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Ortho-McNeil Janssen Scientific Affairs, LLC
INDUSTRY
Mclean Hospital
OTHER
Responsible Party
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James I. Hudson, MD
Professor of Psychiatry, Harvard Medical School
Principal Investigators
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James I Hudson, M.D., Sc.D.
Role: PRINCIPAL_INVESTIGATOR
Mclean Hospital
Harrison G Pope, M.D.
Role: PRINCIPAL_INVESTIGATOR
Mclean Hospital
Locations
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McLean Hospital
Belmont, Massachusetts, United States
Countries
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References
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Hudson JI, Lalonde JK, Coit CE, Tsuang MT, McElroy SL, Crow SJ, Bulik CM, Hudson MS, Yanovski JA, Rosenthal NR, Pope HG Jr. Longitudinal study of the diagnosis of components of the metabolic syndrome in individuals with binge-eating disorder. Am J Clin Nutr. 2010 Jun;91(6):1568-73. doi: 10.3945/ajcn.2010.29203. Epub 2010 Apr 28.
Other Identifiers
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2005-P-000779
Identifier Type: -
Identifier Source: org_study_id
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