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NCT05916417 · ClinicalTrials.gov registry record · NA

TMS-fNIRS Personalized Dosing

A NA study of Post Traumatic Stress Disorder and Traumatic Brain Injury, sponsored by Florida State University.

Recruiting
Registry status
NA
Development phase
60
Enrollment target
1
Study location

NCT05916417: Recruiting NA study of Post Traumatic Stress Disorder and Traumatic Brain Injury, sponsored by Florida State University.

NCT05916417 is a NA study of Post Traumatic Stress Disorder and Traumatic Brain Injury that is actively recruiting participants, run by Florida State University. The registered enrollment target is 60 participants, below the 664-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05916417, a NA study of Post Traumatic Stress Disorder and Traumatic Brain Injury, is actively recruiting participants, sponsored by Florida State University.

RECRUITING
Registry status
NA
Development phase
60 participants
Enrollment target
1
Study location

Study Summary

The intent of this study is to establish technical feasibility in a clinical population (PTSD, with or without mild TBI) of personalized TMS-fNIRS technology. Thereby demonstrating the utility of transcranial magnetic stimulation - functional near-infrared spectroscopy (TMS-fNIRS) technology as a direct measure of frontal brain activity, potentially replacing the indirect motor threshold procedure that may lead to improper dosing of TMS. Personalized TMS-fNIRS technology will guide therapy for depression, post-traumatic stress disorder (PTSD), and/or traumatic brain injury (TBI)

Primary Outcome

The magnitude of brain activation based on fNIRS signal for the respective cortices at the individual level will be assessed and compared for the MC and dl-PFC.

Interventions

  • DEVICE TMS-fNIRS over the dl-PFC

Study Locations (1)

Florida

  • Isabelle Taylor - Tallahassee

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2024-01-19
Est. Completion 2026-09-30
Phase NA
Florida State University

219 total trials

What NCT05916417 shows while recruiting

NCT05916417 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 664-participant average among 262 other Post Traumatic Stress Disorder trials with a reported enrollment target (91% lower).

The record links to 2 conditions, with Post Traumatic Stress Disorder appearing as the primary indexed condition, and to 1 intervention - of which TMS-fNIRS over the dl-PFC is the first listed.

NCT05916417 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT05916417 about?

NCT05916417 is a clinical study titled "TMS-fNIRS Personalized Dosing". The intent of this study is to establish technical feasibility in a clinical population (PTSD, with or without mild TBI) of personalized TMS-fNIRS technology. Thereby demonstrating the utility of transcranial magnetic stimulation - functional near-infrared spectroscopy (TMS-fNIRS) technology as a di...

What is the current status of trial NCT05916417?

This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2024-01-19. Estimated completion is 2026-09-30.

What conditions does trial NCT05916417 study?

This clinical trial studies the following conditions: Post Traumatic Stress Disorder, Traumatic Brain Injury.

What interventions are being tested in trial NCT05916417?

The interventions under investigation include: TMS-fNIRS over the dl-PFC (DEVICE).

Who is sponsoring clinical trial NCT05916417?

This trial is sponsored by Florida State University, which has 219 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05916417 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Post Traumatic Stress Disorder

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05916417's enrollment target sits among peer trials

60 160th of 262 higher than 96 of 262 other Post Traumatic Stress Disorder trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Post Traumatic Stress Disorder trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05916417, the US trial registry maintained by the National Library of Medicine. NCT05916417 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.