EXOMIND Device for OCD
What You Need to Know Before You Apply
What is the purpose of this trial?
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
Are You a Good Fit for This Trial?
This trial is for adults aged 22 and older who have obsessive-compulsive disorder (OCD).Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Interventions
- EXOMIND (BTL-699-2) Active treatment
Trial Overview
The study tests the EXOMIND (BTL-699-2) device, which uses repetitive transcranial magnetic stimulation (rTMS), to see if it can safely reduce OCD symptoms. Participants are randomly assigned to receive either real or sham (inactive) treatment.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Placebo Group
Participants will receive active treatment (BTL-699-2 intensity: up to 80% of MT)
Participants will receive sham treatment (BTL-699-2 intensity: 5% of MT)
Find a Clinic Near You
Who Is Running the Clinical Trial?
BTL Industries Ltd.
Lead Sponsor
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