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ENROLLING BY INVITATION
NCT06512324

Operation of Brain Stimulation Equipment Under Remote Viewing Effectiveness Registry

Sponsor: Biomedical Discoveries and Neuroscientific Foundations LLC

View on ClinicalTrials.gov

Summary

The goal of this observational study is to record and analyze factors putatively affecting the clinical outcomes among patients undergoing transcranial magnetic stimulation (TMS) treatment for major depressive disorder (MDD) or generalized anxiety disorder (GAD). The main questions it aims to answer are: 1. Which factors have the greatest causal role in mediating the effectiveness of TMS in improving symptoms of depression (and/or anxiety)? 2. Which factors have a minimal causal role in mediating the effectiveness of TMS in improving symptoms of depression (and/or anxiety)? Participants already undergoing TMS as part of their treatment plan for MDD/GAD answer survey questions about their symptoms before, during, and up to 1 year post-treatment. Factors affecting clinical outcomes such as stimulation parameters, behavioral factors, physiological factors, patient characteristics, and pharmacological factors, are also recorded.

Official title: Operation of Brain Stimulation Equipment Under Remote Viewing Effectiveness Registry (OBSERVER)

Key Details

Gender

All

Age Range

12 Years - Any

Study Type

OBSERVATIONAL

Enrollment

5000

Start Date

2024-06-27

Completion Date

2029-12-31

Last Updated

2024-07-22

Healthy Volunteers

No

Interventions

DEVICE

Ampa One TMS System

Transcranial Magnetic Stimulation

Locations (2)

Kind Health Group

Encinitas, California, United States

Salience Research Institute

Plano, Texas, United States