Incentive Processing and Learning in Anorexia Nervosa and Bulimia Nervosa
NCT ID: NCT05056597
Last Updated: 2025-03-27
Study Results
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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RECRUITING
252 participants
OBSERVATIONAL
2022-05-26
2027-01-31
Brief Summary
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Aim 1: To examine neural differences in 'liking' and 'wanting' in ED relative to HC.
Aim 2: To examine differences in instrumental learning for reward and punishment in ED relative to HC.
Aim 3: To examine how 'liking' and 'wanting' drive instrumental learning in ED and predict clinical symptoms at baseline and 1 year later.
Exploratory Aim: To explore the associations of dopamine function, as measured by neuromelanin MRI (NM-MRI), with ED diagnosis and brain response to 'liking', 'wanting', and learning.
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
CROSS_SECTIONAL
Study Groups
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AN-R
Participants that meet Diagnostic And Statistical Manual Of Mental Disorders (DSM-V) criteria for Anorexia Nervosa restricting subtype.
No interventions assigned to this group
AN-BP
Participants that meet DSM-V criteria for Anorexia Nervosa binging/purging subtype
No interventions assigned to this group
BN
Participants that meet DSM-V criteria for Bulimia Nervosa.
No interventions assigned to this group
Healthy Controls
Participants that do not meet DSM-V criteria for any disorder.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Between the ages of 18 and 39 years old
* Meet DSM-V criteria for AN-R, AN-BP, or BN
Healthy Control Group:
* Between the ages of 18 and 39 years old
* Have maintained 85% to 120% ideal body weight since menarche
Exclusion Criteria
* Psychotic illness/other mental illness requiring hospitalization
* Current dependence on drugs or alcohol defined by DSM IV criteria. Additionally, positive test results for drug use on the day of the scan, apart of marijuana, will result in cancelling or rescheduling the scan because acute use will impact MRI measures.
* Physical conditions (e.g. diabetes mellitus, pregnancy) known to influence eating or weight
* Neurological disorder, neurodevelopmental disorder, or history of head injury with \>30 min loss of consciousness
* Any contraindication to undergoing an MRI
* Primary obsessive compulsive disorder or primary major depressive disorder
-If taking other psychotropic medication, any change in dosage in the 2 weeks before scanning
* Meet criteria for the diagnosis of any psychiatric disorder currently
* Any history of binge eating or purging behaviors, including self-induced vomiting, laxative or diuretic misuse
* Use of any psychoactive or other medication known to affect mood or concentration in the last 3 months
18 Years
39 Years
FEMALE
Yes
Sponsors
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University of California, San Diego
OTHER
Responsible Party
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Christina Wierenga
Professor
Locations
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UCSD Eating Disorders Treatment and Research Program
La Jolla, California, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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800775
Identifier Type: -
Identifier Source: org_study_id
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