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NCT07679750 · ClinicalTrials.gov registry record · NA

rTMS Device for Improvement of Obsessive and Compulsive Behaviors

A NA study, sponsored by BTL Industries.

Not yet
Registry status
NA
Development phase
60
Enrollment target

NCT07679750 is a NA study that has not yet begun recruiting, run by BTL Industries. The registered enrollment target is 60 participants.

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The verdict

NCT07679750, a NA study, has not yet begun recruiting, sponsored by BTL Industries.

NOT YET RECRUITING
Registry status
NA
Development phase
60 participants
Enrollment target

Study 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

Interventions

  • DEVICE EXOMIND (BTL-699-2) Active treatment
  • DEVICE EXOMIND (BTL-699-2) Sham treatment

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2026-06-24
Est. Completion 2026-12
Phase NA

Sponsor

BTL Industries

40 total trials

What the Registry Record Tells You About NCT07679750

The ClinicalTrials.gov registry entry for NCT07679750 describes a study currently listed as not yet recruiting, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is BTL Industries, which has 40 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which EXOMIND (BTL-699-2) Active treatment is the first listed.

NCT07679750 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT07679750 about?

NCT07679750 is a clinical study titled "rTMS Device for Improvement of Obsessive and Compulsive Behaviors". 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...

What is the current status of trial NCT07679750?

This trial is currently not yet recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2026-06-24. Estimated completion is 2026-12.

What interventions are being tested in trial NCT07679750?

The interventions under investigation include: EXOMIND (BTL-699-2) Active treatment (DEVICE), EXOMIND (BTL-699-2) Sham treatment (DEVICE).

Who is sponsoring clinical trial NCT07679750?

This trial is sponsored by BTL Industries, which has 40 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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