Self-regulatory Control and Eating: A Neuroimaging Study of Bulimia Nervosa

NCT ID: NCT01935401

Last Updated: 2014-10-07

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 47 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2011-06-30

Brief Summary

The purpose of this study will be to replicate previous findings of deficits in prefrontal activation during response inhibition tasks in bulimia nervosa and extend these findings by demonstrating similar deficiencies in activity during a functional behavioral task that requires the inhibition of eating. Findings from this study will potentially help to elucidate the underlying neural mechanisms of bulimia nervosa, and thus inform treatment and prevention efforts.

Detailed Description

Bulimia nervosa (BN), is a serious psychiatric disorder that has high rates of comorbidity and often results in role impairment for the suffer. Thus far, although psychosocial and behavioral risk factors and correlates of BN have been extensively researched, relatively few studies have focused on brain-based determinants of BN. Identification of neural mechanisms associated with self-regulatory control that may be integral in the development, maintenance, and prevention of this debilitating condition would better inform treatment development and eating disorder prevention efforts.

Participation in this study consists of a 3-3.5 hours study visit as well a a one year follow up visit. The first portion of initial study visit is part of the screening process, in which individuals will complete several questionnaires and be interviewed by the study researcher in order to confirm eligibility. If a participant is eligible after the screening portion, they move onto the rest of the initial visit. During the initial visit, participants will complete a button pressing go/no-go task as well as a sipping go/no-go task, all while wearing a functional near-infrared spectroscopy (fNIR) device.

At a one year follow up appointment, individuals will again complete a variety of self-report questionnaires and be interviewed by the study researcher, thus completing the same measures used as screening tools in the initial visit.

Conditions

Bulimia Nervosa

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: PROSPECTIVE

Study Groups

Women with Bulimia Nervosa

fNIR

• Functional near-infrared spectroscopy measured-brain activity

No interventions assigned to this group

Healthy Controls

fNIR

• Functional near-infrared spectroscopy measured-brain activity

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Female
• Right-handed
• Age 18-45
• Between 85 and 120% of ideal body weight based on height
• Currently meeting proposed DSM-5 criteria for Bulimia Nervosa (at least one objective bulimic episode and compensatory purging episode per week for the past three months)
• Purging via self-induced vomiting
• Duration of illness of at least 6 months

Exclusion Criteria

• Current significant medical illness
• Any disorder or condition resulting in difficulty swallowing (e.g., dysphagia)
• History of neurological disorders or diseases (e.g., stroke, seizures, heart disease, head trauma with loss of consciousness)
• Drug or alcohol abuse in the past 6 months or any history of alcohol or drug dependence
• Use of marijuana or any other illegal drug (e.g., cocaine, heroin, ecstasy) in the week before the study visit
• IQ less than 75
• Pregnancy, lactation, or planning to become pregnant in the next year
• Allergy to sucrose, dairy, wheat, gluten, apples (i.e., any of the ingredients in the strawberry yogurt shake or in the standardized meal prior to study participation)
• Participants rating the strawberry yogurt shake as a 5 or lower on a 9-point category scale of liking will be excluded from further study
• Meeting the criteria for a diagnosis of Attention Deficit Hyperactivity Disorder
• Any other current major Axis I disorder, other than major depressive disorder (MDD) or generalized anxiety disorder (GAD)
• Inability to consent
• Prisoner

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Michael Lowe

OTHER

Sponsor Role: lead

Responsible Party

Michael Lowe

PI

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Michael R Lowe, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Drexel University

Locations

Drexel University

Philadelphia, Pennsylvania, United States

Countries

United States

Other Identifiers

1F31MH097406

Identifier Type: NIH

Identifier Source: org_study_id

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