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Brain study seeks to unlock reward learning in anorexia

NCT ID NCT05531604

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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)

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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

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Other studies related to the condition(s) this trial covers.