rTMS Device for Improvement of Obsessive and Compulsive Behaviors
NCT: NCT07679750 · NOT_YET_RECRUITING
Brief Summary
The goal of this investigational study is to evaluate if the treatment using EXOMIND(BTL-699-2) device is able to improve severity of obsessive and compulsive symptoms in adults (aged 22 and older). The main question it aims to answer is: Does the treatment using EXOMIND (BTL-699-2) device is able safely and efficiently reduce the severity of obsessive and compulsive behaviors? Participants will be asked to: * Complete six treatment visits (twelve treatment sessions) * Complete The Yale-Brown Obsessive-Compulsive Severity Scale Second Edition Self Report Version (Y-BOCS-II SR) * Complete Short UPPS-P Impulsive Behaviour Scale (SUPPS-P) * Compete The Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS) * Compete The Patient Health Questionnaire-9 (PHQ-9) * Compete Columbia Suicide Severity Rating Scale -screen version(CSSRS) * Complete Trigger Recall Experience Questionnaire (only for participants who agree to participate in trigger recall procedure during the treatment sessions) * Compete The Therapy Comfort Questionnaire * Compete The Subject Satisfaction Questionnaire
Frequently Asked Questions
What is rTMS Device for Improvement of Obsessive and Compulsive Behaviors?
rTMS Device for Improvement of Obsessive and Compulsive Behaviors is a clinical trial registered under NCT07679750. Current status: NOT_YET_RECRUITING.
What is the status of NCT07679750?
The current status of NCT07679750 (rTMS Device for Improvement of Obsessive and Compulsive Behaviors) is: NOT_YET_RECRUITING.
When did rTMS Device for Improvement of Obsessive and Compulsive Behaviors start?
rTMS Device for Improvement of Obsessive and Compulsive Behaviors started on 2026-06-24.
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Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.