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NCT04220112 · ClinicalTrials.gov registry record · NA

Comparing Real-time fMRI Neurofeedback Versus Sham for Altering Limbic and Eating Disturbances in Anorexia Nervosa

A NA study of Anorexia Nervosa and Anorexia, sponsored by University of Minnesota.

Completed
Registry status
NA
Development phase
33
Enrollment target
1
Study location

NCT04220112 is a NA study of Anorexia Nervosa and Anorexia that has completed, run by University of Minnesota. The registered enrollment target is 33 participants, below the 949-participant average among 43 other Anorexia Nervosa trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04220112, a NA study of Anorexia Nervosa and Anorexia, has completed, sponsored by University of Minnesota.

COMPLETED
Registry status
NA
Development phase
33 participants
Enrollment target
1
Study location

Study Summary

The goal of the purposed research is to extend prior work (STUDY00003758: Real-time fMRI Neurofeedback to Alter Limbic Disturbances in Anorexia Nervosa) on real-time fMRI (rt-fMRI) neurofeedback (focused on amygdala down-regulation) as an innovative neurocircuitry-targeted intervention for anorexia nervosa (AN). This project will include randomization to rt-fMRI or a sham controlled group to answer the following important unresolved question: Does a patient-led procedure aimed at altering brain activity impact limbic circuit function and key eating disorder and psychiatric symptoms in AN above the effect of a matched, but non-targeted sham condition?

Interventions

  • PROCEDURE Sham Procedure
  • PROCEDURE Real-Time Functional Magnetic Resonance Imaging (RT-fMRI)

Study Locations (1)

Minnesota

  • University of Minnesota - Minneapolis

Trial Details

FieldValue
Enrollment Target 33 participants
Start Date 2020-03-01
Est. Completion 2022-09-30
Phase NA

Sponsor

University of Minnesota

966 total trials

What the Registry Record Tells You About NCT04220112

The ClinicalTrials.gov registry entry for NCT04220112 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 33 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 949-participant average among 43 other Anorexia Nervosa trials with a reported enrollment target (97% lower). The listed sponsor is University of Minnesota, which has 966 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Anorexia Nervosa appearing as the primary indexed condition, and to 2 interventions - of which Sham Procedure is the first listed.

NCT04220112 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.

Frequently Asked Questions

What is clinical trial NCT04220112 about?

NCT04220112 is a clinical study titled "Comparing Real-time fMRI Neurofeedback Versus Sham for Altering Limbic and Eating Disturbances in Anorexia Nervosa". The goal of the purposed research is to extend prior work (STUDY00003758: Real-time fMRI Neurofeedback to Alter Limbic Disturbances in Anorexia Nervosa) on real-time fMRI (rt-fMRI) neurofeedback (focused on amygdala down-regulation) as an innovative neurocircuitry-targeted intervention for anorexia ...

What is the current status of trial NCT04220112?

This trial is currently completed. It is a NA study. The enrollment target is 33 participants. The study started on 2020-03-01. Estimated completion is 2022-09-30.

What conditions does trial NCT04220112 study?

This clinical trial studies the following conditions: Anorexia Nervosa, Anorexia.

What interventions are being tested in trial NCT04220112?

The interventions under investigation include: Sham Procedure (PROCEDURE), Real-Time Functional Magnetic Resonance Imaging (RT-fMRI) (PROCEDURE).

Who is sponsoring clinical trial NCT04220112?

This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04220112 being conducted?

This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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