Viewing Study NCT06512324



Ignite Creation Date: 2024-10-26 @ 3:35 PM
Last Modification Date: 2024-10-26 @ 3:35 PM
Study NCT ID: NCT06512324
Status: ENROLLING_BY_INVITATION
Last Update Posted: None
First Post: 2024-07-16

Brief Title: Operation of Brain Stimulation Equipment Under Remote Viewing Effectiveness Registry
Sponsor: None
Organization: None

Study Overview

Official Title: Operation of Brain Stimulation Equipment Under Remote Viewing Effectiveness Registry OBSERVER
Status: ENROLLING_BY_INVITATION
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: OBSERVER
Brief 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 andor anxiety
2 Which factors have a minimal causal role in mediating the effectiveness of TMS in improving symptoms of depression andor anxiety

Participants already undergoing TMS as part of their treatment plan for MDDGAD 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None