Condition: Eating Disorders · Anxiety · Sponsor: Rogers Behavioral Health
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.
This description comes directly from the study's public registry record.
Hana F Zickgraf, Ph.D. · 262-303-0170 · hana.zickgraf@rogersbh.org
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| Rogers Behavioral Health | Oconomowoc, Wisconsin, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07017322