Please sign in to follow a disease.
Brain study seeks to unlock reward learning in anorexia
NCT ID NCT05531604
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at how people with anorexia nervosa learn to associate positive feelings with sounds like baby laughter. Researchers will measure brain activity, heart rate, and pupil responses in 90 females aged 12-22. The goal is to understand if and how positive associations are formed and remembered, which could inform future treatments.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this research could reveal how reward learning works in anorexia, potentially guiding future therapies.
- What could go wrong
- This is an observational study, not a treatment trial. It may not lead directly to new treatments, and results may not apply to all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
About 90 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Sep 2022
- Expected to finish
-
Jun 2026
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Investigators will enroll 90 female participants between the ages of 12 and 22 (30 with current anorexia nervosa - restricting type, 30 with a history of anorexia nervosa - restricting type, and 30 non-clinical healthy controls).
- Ages
-
12 to 22 years
- Sex
-
Female participants only
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. AN-Restricting (AN-R) Group 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: Inclusion criteria: 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: Inclusion criteria: 1. Healthy females from any racial or ethnic background 2. Ages 12-22 years Exclusion Criteria: * AN-R and History of AN-R groups: 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)
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Anorexia nervosa are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Centre for Addiction and Mental Health
Toronto, Ontario, M6J 1H3, Canada
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can the Brain's Information-Integration process explain Anorexia's grip?
- Can a pudding snack reveal how the brain misreads the stomach?
- Could the gut microbiome hold clues to eating disorder recovery?
- Can a parent support group help teens with both autism and anorexia?
- Lab-Grown brain cells could unlock Anorexia's secrets
- Can science unlock the secrets of the naturally lean?