Emotion Regulation in Binge Eating and Purging Among Adolescents

NCT ID: NCT03429114

Last Updated: 2022-12-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

47 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-10-15

Study Completion Date

2022-09-01

Brief Summary

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The study will examine the neural and behavioral correlates of emotion regulation in adolescents engaging in binge eating and/or purging and healthy adolescents. Furthermore, it will look at the influence of executive function on emotion regulation in this population. This study will allow us to gain further understanding of the neural basis of emotion regulation in this age group. Moreover, this study supports the need to develop new treatment approaches based on a better understanding of the brain processes associated with eating disorders.

Detailed Description

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Conditions

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Binge Eating Purging (Eating Disorders)

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Binge eating/purging

Adolescents engaging in recurrent binge eating and/or purging behavior.

Magnetic resonance imaging

Intervention Type OTHER

We will conduct MRI and fMRI brain scans to compare brain function between groups.

Healthy comparison

Adolescents who do not have a history of eating disorders

Magnetic resonance imaging

Intervention Type OTHER

We will conduct MRI and fMRI brain scans to compare brain function between groups.

Interventions

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Magnetic resonance imaging

We will conduct MRI and fMRI brain scans to compare brain function between groups.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Female
* Ages 14-18
* with or without current binge eating and/or purging behaviors

Exclusion Criteria

We exclude patients of clinically significant low weight (\<85% ideal body weight using CDC norms for height, age, and gender) and those with contraindications for MRI (e.g., orthodontia, metallic implants). Participants also will be without evidence of current or past major neurological (e.g., seizures, psychosis, head trauma) or major sensory deficit.
Minimum Eligible Age

14 Years

Maximum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Stanford University

OTHER

Sponsor Role lead

Responsible Party

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Cara Bohon, PhD

Assistant Professo

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Stanford University, Department of Psychiatry

Stanford, California, United States

Site Status

Countries

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United States

Other Identifiers

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40075

Identifier Type: -

Identifier Source: org_study_id

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