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
90 participants
OBSERVATIONAL
2022-09-30
2026-06-30
Brief Summary
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In this study, the investigators will identify the patterns of how those with AN acquire positive associations, how they diminish, and their relationships to physiology (heart rate and pupil responses) and brain activation. In assessing the robustness of this learning, the investigators will investigate the extent to which this association is reactivated after 24 hours, and the extent to which a memory prompt will help reinstate this previously learned positive association.
This project will allow for important advances in our understanding of the neurobiology of AN. The investigators will first identify if, and how, those with AN come to learn positive associations to cues, and secondly, the extent to which learned positive associations remain over time. Moreover, the investigators will use machine learning to ascertain whether reward learning can be predicted by physiological and neural biomarkers.
Detailed Description
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Conditions
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Keywords
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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AN-Restricting (AN-R)
Meet Diagnostic and Statistical Manual (DSM-5) criteria for anorexia nervosa, restricting subtype
appetitive conditioning
The investigators will examine acquisition and extinction of learned associations to positively-valenced, socially rewarding yet symptom-neutral infant laughter sounds in an appetitive conditioning paradigm. The investigators will also examine spontaneous recovery of this association 24 hours later when re-presented with these cues, and the reinstatement of this association when re-exposed to infant laughter.
Weight Restored AN-Restricting (WRAN-R)
* History of anorexia nervosa, restricting type - previously meeting full DSM-5 criteria.
* Eating Disorder Examination Questionnaire (EDE-Q) ≤ 2 (within 1 standard deviation \[SD\] of community norms and lower than 1 standard deviation from clinical norms for female anorexia nervosa, restricting type populations)
appetitive conditioning
The investigators will examine acquisition and extinction of learned associations to positively-valenced, socially rewarding yet symptom-neutral infant laughter sounds in an appetitive conditioning paradigm. The investigators will also examine spontaneous recovery of this association 24 hours later when re-presented with these cues, and the reinstatement of this association when re-exposed to infant laughter.
Healthy controls
Healthy females from any racial or ethnic background, not meeting DSM-5 criteria for any psychiatric disorder.
appetitive conditioning
The investigators will examine acquisition and extinction of learned associations to positively-valenced, socially rewarding yet symptom-neutral infant laughter sounds in an appetitive conditioning paradigm. The investigators will also examine spontaneous recovery of this association 24 hours later when re-presented with these cues, and the reinstatement of this association when re-exposed to infant laughter.
Interventions
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appetitive conditioning
The investigators will examine acquisition and extinction of learned associations to positively-valenced, socially rewarding yet symptom-neutral infant laughter sounds in an appetitive conditioning paradigm. The investigators will also examine spontaneous recovery of this association 24 hours later when re-presented with these cues, and the reinstatement of this association when re-exposed to infant laughter.
Eligibility Criteria
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Inclusion Criteria
1. Females from any racial or ethnic background
2. Ages between 12 and 22 years
3. Meet DSM-5 criteria for AN - restricting subtype
4. Medically stable designated by their physician in the past month (having any of the following measurements taken by a physician or nurse within the past month preceding the telephone screen: (i) orthostasis: drop in systolic blood pressure \> 20 mm Hg or diastolic blood pressure \> 10 mm Hg, or an increase in heart rate (HR) \> 20 bpm upon standing for 3 minutes after lying down; (ii) resting HR \<45; or (iii) resting blood pressure of \<80 mm Hg systolic or \<50 mm Hg diastolic 99. Prospective participants who do not meet the medical instability criteria and otherwise pass the telephone screen, will be invited to proceed to the consent process. If they have not had these measurements done in the month prior, we will encourage them to visit their doctor or nurse to have these done and then to recontact us with the results ):
5. BP and pulse measured at the day of the scan by the investigators
* Heart rate ≥ 45 at rest
* Resting blood pressure of ≥80 mm Hg systolic and ≥50 mm Hg diastolic
* Lying and standing (after 3 min.) BP drop of ≤20 systolic and ≤10 diastolic and increase in HR ≤20 bpm
6. Not taking psychiatric medications or taking serotonin-reuptake inhibitor or serotonin-norepinephrine reuptake inhibitor medications at stable doses
2. History of AN-Restricting Group:
1. Females from any racial or ethnic background
2. Ages between 12 and 22 years
3. EDE-Q ≤ 2 (puts them within 1 standard deviation \[SD\] of community norms and lower than 1 SD from clinical norms for female AN-R)
4. History of AN - meeting full criteria, diagnosed by a licensed clinician
5. Not taking psychiatric medications or taking serotonin-reuptake inhibitor or serotonin-norepinephrine reuptake inhibitor medications at stable doses
3. Healthy controls:
1. Healthy females from any racial or ethnic background
2. Ages 12-22 years
Exclusion Criteria
1. Antipsychotic medications
2. Change in dose of psychotropic medication over the previous 4 weeks
3. Current psychotic disorder
Healthy controls:
1. Any current Axis I disorder
2. Eating Disorder Examination Questionnaire score greater than established community norms (\>2)
3. Met criteria for AN (in the past or present)
All:
1. Neurological disorder
2. Infants or children of their own
3. Pregnancy
4. Current risk of suicide with a plan and intent
5. Ferromagnetic metal implantations or devices (electronic implants or devices, infusion pumps, aneurysm clips, metal fragments or foreign bodies, metal prostheses, joints, rods or plates)
12 Years
22 Years
FEMALE
Yes
Sponsors
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University of Southern California
OTHER
University of Toronto
OTHER
California Institute of Technology
OTHER
Klarman Family Foundation
UNKNOWN
Centre for Addiction and Mental Health
OTHER
Responsible Party
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Principal Investigators
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Jamie D Feusner, M.D.
Role: PRINCIPAL_INVESTIGATOR
Centre for Addiction and Mental Health
Stuart Murray, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
University of Southern California
Locations
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Centre for Addiction and Mental Health
Toronto, Ontario, Canada
Countries
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Central Contacts
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Facility Contacts
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Jamie D Feusner, M.D.
Role: primary
References
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Murray SB, Zbozinek TD, Craske M, Tadayonnejad R, Strober M, Bari AA, O'Doherty JP, Feusner JD. Neural, physiological, and psychological markers of appetitive conditioning in anorexia nervosa: a study protocol. J Eat Disord. 2022 May 10;10(1):68. doi: 10.1186/s40337-022-00546-5.
Related Links
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Published manuscript of the study protocol
Other Identifiers
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20202201
Identifier Type: -
Identifier Source: org_study_id