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NCT06624150 · ClinicalTrials.gov registry record · Phase 1

tDCS and Cognitive Training for Restrictive Eating Disorders

A Phase 1 study of Anorexia Nervosa and Atypical Anorexia Nervosa, sponsored by University of Minnesota.

Recruiting
Registry status
Phase 1
Development phase
20
Enrollment target
1
Study location

NCT06624150 is a Phase 1 study of Anorexia Nervosa and Atypical Anorexia Nervosa that is actively recruiting participants, run by University of Minnesota. The registered enrollment target is 20 participants, below the 950-participant average among 43 other Anorexia Nervosa trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06624150, a Phase 1 study of Anorexia Nervosa and Atypical Anorexia Nervosa, is actively recruiting participants, sponsored by University of Minnesota.

RECRUITING
Registry status
Phase 1
Development phase
20 participants
Enrollment target
1
Study location

Study Summary

This study looks at adults with restrictive eating disorders who are currently receiving outpatient treatment for their eating disorder to examine whether a new brain stimulation technique called non-invasive transcranial direct current stimulation (tDCS) can enhance brain training. Participation involves interviews, assessments, 10 sessions of brain stimulation (active or sham), and computerized brain training over a 3-4 week period, with one post-intervention visit, and one 1-month follow-up visit.

Conditions Studied

Anorexia Nervosa Atypical Anorexia Nervosa

Interventions

  • DEVICE Active tDCS sessions, StarStim device
  • DEVICE Sham (fake) tDCS sessions

Study Locations (1)

Minnesota

  • University of Minnesota - Minneapolis

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2024-08-02
Est. Completion 2026-06-02
Phase Phase 1

Sponsor

University of Minnesota

966 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06624150

The ClinicalTrials.gov registry entry for NCT06624150 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 950-participant average among 43 other Anorexia Nervosa trials with a reported enrollment target (98% 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 Active tDCS sessions, StarStim device is the first listed.

NCT06624150 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.

Frequently Asked Questions

What is clinical trial NCT06624150 about?

NCT06624150 is a clinical study titled "tDCS and Cognitive Training for Restrictive Eating Disorders". This study looks at adults with restrictive eating disorders who are currently receiving outpatient treatment for their eating disorder to examine whether a new brain stimulation technique called non-invasive transcranial direct current stimulation (tDCS) can enhance brain training. Participation in...

What is the current status of trial NCT06624150?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2024-08-02. Estimated completion is 2026-06-02.

What conditions does trial NCT06624150 study?

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

What interventions are being tested in trial NCT06624150?

The interventions under investigation include: Active tDCS sessions, StarStim device (DEVICE), Sham (fake) tDCS sessions (DEVICE).

Who is sponsoring clinical trial NCT06624150?

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

Where is trial NCT06624150 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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.