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

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. According to ClinicalTrials.gov, the official US trial registry.

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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.

Primary Outcome

Feasibility and tolerability measure 1. Evaluating for less than 20% dropout over the course of the tDCS for R-EDs study.

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
University of Minnesota

966 total trials

What NCT06624150 shows while recruiting

NCT06624150 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 950-participant average among 43 other Anorexia Nervosa trials with a reported enrollment target (98% lower).

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 a single indexed study location in 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.

Similar trials for Anorexia Nervosa

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06624150's enrollment target sits among peer trials

20 35th of 43 higher than 5 of 43 other Anorexia Nervosa trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Anorexia Nervosa trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06624150, the US trial registry maintained by the National Library of Medicine. NCT06624150 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.