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EEG for Prediction Error in Anorexia

N/A
Waitlist Available
Led By Guido Frank, MD
Research Sponsored by University of California, San Diego
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Healthy body weight between 90 and 110 % average body weight.
Healthy body weight between 90 and 110 % average body weight
Timeline
Screening 3 weeks
Treatment Varies
Follow Up immediate during brain scanning
Awards & highlights

Study Summary

This trial is testing the feasibility of using electroencephalography (EEG) to study adolescent anorexia nervosa (AN), with the goal of eventually replacing more costly and difficult-to-access fMRI.

Who is the study for?
This trial is for girls aged 11-17 with Anorexia Nervosa (AN), specifically the restricting type, and healthy controls within a similar age range. Participants must have a body weight below 17.5 BMI if diagnosed with AN or between 90-110% of average body weight if they are healthy controls. All participants should be right-handed as per the Edinburgh Handedness Inventory, speak English primarily, and for those with AN, be in their first weeks of treatment at specified centers.Check my eligibility
What is being tested?
The study aims to develop an EEG-based method to investigate prediction error responses in adolescents with AN compared to healthy controls. It will adapt existing fMRI protocols for EEG use and test whether these can reliably measure brain responses related to reward processing errors across different stimuli like taste and money.See study design
What are the potential side effects?
Since this trial involves non-invasive EEG testing rather than medication or invasive procedures, there are minimal expected side effects. The main concerns may include discomfort from wearing the EEG cap or stress from participating in the tasks required by the study.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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My weight is within the normal range for my height.
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My weight is within the normal range for my height.
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I am diagnosed with anorexia, have a BMI under 17.5, fear gaining weight, see my body differently, and if applicable, haven't had a menstrual cycle for over three months.
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I am in my first 1-2 weeks of treatment at UC San Diego or Rady Children's Hospital.
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I am in my first 1-2 weeks of treatment at UC San Diego or Rady Children's Hospital.
Select...
I am diagnosed with anorexia, have a BMI under 17.5, fear gaining weight, see my body differently, and if applicable, haven't had a menstrual cycle for over three months.
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I am a female between 11 and 17 years old.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~immediate during brain scanning
This trial's timeline: 3 weeks for screening, Varies for treatment, and immediate during brain scanning for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Electroencephalography
Monetary Reward Prediction Error Brain Response using EEG will show similar regional brain response compared to taste prediction error response.
Reward Prediction Error Brain Response using Electroencephalography (EEG) to separate healthy controls from individuals with anorexia nervosa.

Trial Design

2Treatment groups
Experimental Treatment
Group I: Healthy Control GroupExperimental Treatment1 Intervention
Participants who are considered to be healthy controls
Group II: Anorexia Nervosa GroupExperimental Treatment1 Intervention
Participants with anorexia nervosa

Find a Location

Who is running the clinical trial?

University of California, San DiegoLead Sponsor
1,119 Previous Clinical Trials
1,521,461 Total Patients Enrolled
15 Trials studying Anorexia Nervosa
1,570 Patients Enrolled for Anorexia Nervosa
Guido Frank, MDPrincipal Investigator - University of California, San Diego
University of California, San Diego
5 Previous Clinical Trials
431 Total Patients Enrolled
5 Trials studying Anorexia Nervosa
431 Patients Enrolled for Anorexia Nervosa

Media Library

Anorexia Nervosa Group Clinical Trial Eligibility Overview. Trial Name: NCT04583774 — N/A
Anorexia Nervosa Research Study Groups: Anorexia Nervosa Group, Healthy Control Group
Anorexia Nervosa Clinical Trial 2023: Anorexia Nervosa Group Highlights & Side Effects. Trial Name: NCT04583774 — N/A
Anorexia Nervosa Group 2023 Treatment Timeline for Medical Study. Trial Name: NCT04583774 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there any open enrollment slots for this medical trial?

"Affirmative. Perusal of the clinicaltrials.gov website reveals that this medical study, which was inaugurated on February 9th 2021, is still open for recruitment. A total of 44 patients need to be sourced from 1 centre."

Answered by AI

How many participants are currently involved in this research investigation?

"Affirmative. Per the information on clinicaltrials.gov, this medical experiment is currently recruiting subjects; it was first uploaded to the site on February 9th 2021 and its details were most recently modified April 1st 2022 . In total 44 individuals will be accepted from a single trial location."

Answered by AI

Is it possible to participate in this medical experiment?

"To be accepted, potential study participants must have a diagnosis of anorexia nervosa and fall within the 11 to 17 year-old age range. Approximately 44 people will be admitted into this trial."

Answered by AI

Is the recruitment phase of this study inclusive to elderly participants?

"This medical study permits candidates aged 11 to 17 only. There are 38 trials aimed at minors and 33 for elderly participants."

Answered by AI
~1 spots leftby Jun 2024