Non-invasive Cranial Electrical Stimulation for Mealtime Anxiety in Adults With Eating Disorders

The study is to evaluate the feasibility of using a non-invasive brain stimulation device in a sample of inpatients with eating disorders (ED). The study will help researchers evaluate whether their device protocol is practical for eating disorder inpatients as a way to manage eating disorder and anxiety symptoms. A secondary aim of the study is to evaluate preliminary effectiveness of the protocol for reducing pre-meal anxiety during the treatment, and explore effects on eating disorder symptoms over the course of the inpatient admission.

NCT Number	NCT07017322
Lead Sponsor	Rogers Behavioral Health Collaborators: Electromedical Products International, Inc.
Conditions	Eating Disorders, Anxiety
Enrollment	30 participants
Start Date	2025-06-03
Primary Completion	2027-11-01 (estimated)
Study Completion	2027-11-01 (estimated)
Updated on ClinicalTrials.gov	2026-08-12