Follow-Up Extension to the Family Study of Binge Eating Disorder

NCT ID: NCT00777634

Last Updated: 2012-05-29

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

268 participants

Study Classification

OBSERVATIONAL

Study Start Date

2005-06-30

Study Completion Date

2009-11-30

Brief Summary

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This study involves a 2.5 and 5 year follow-up interview for individuals who participated in the initial family study of binge eating disorder. The study includes individuals with and without eating disorder as well as their first degree relatives. As part of the study, participants will be interviewed about their current psychiatric and medical symptoms, their blood pressure will be measured, and laboratory specimens will be obtained.

Detailed Description

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Previously we completed a family interview study of 150 individuals with binge eating disorder, 150 matched controls, and approximately 888 of their first degree relatives. In follow-up to this, we are interviewing these individuals again at 2.5 and 5 years after their initial interview. During the course of the interview, individuals are asked about their psychiatric and medical history and blood pressure and laboratory specimens are obtained to measure, among other things, fasting lipids and glucose.

Conditions

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Binge Eating Disorder

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Binge eating disorder (BED)

Individuals who meet criteria for binge eating disorder.

No intervention.

Intervention Type OTHER

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.

Intervention Type OTHER

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.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Individuals with or without binge eating disorder and their family members who participated in the initial family study of binge eating disorder and agree to be followed up at 2.5 and 5 years.

Exclusion Criteria

* Unwilling or unable to participate in the follow-up study.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Ortho-McNeil Janssen Scientific Affairs, LLC

INDUSTRY

Sponsor Role collaborator

Mclean Hospital

OTHER

Sponsor Role lead

Responsible Party

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James I. Hudson, MD

Professor of Psychiatry, Harvard Medical School

Responsibility Role PRINCIPAL_INVESTIGATOR

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

Site Status

Countries

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United States

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.

Reference Type DERIVED
PMID: 20427731 (View on PubMed)

Other Identifiers

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2005-P-000779

Identifier Type: -

Identifier Source: org_study_id

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