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Not yet recruiting NCT06548113

Sensory Synchronized Imaging and Neuromodulation

No phase Interventional Major Depressive Disorder

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: TMS.
Who it may be relevant to
Registry conditions: Major Depressive Disorder. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Investigation of Sensory Synchronized Human Brain Imaging and Neuromodulation

Overview

The purpose of this research study is to better understand the relationship between the type of brain stimulation used and how it changes brain activity in adult military Veterans. The goal is to use this understanding to develop new, personalized brain stimulation. The investigators evaluate brain changes from different types of transcranial magnetic brain stimulation (TMS).

Interventions

  • Device TMS
    transcranial magnetic brain stimulation

Primary outcome measures

  • Transcranial Magnetic Stimulation (TMS) / Electroencephalography (EEG) change [Time frame: 45 minutes]

Eligibility criteria

Inclusion criteria

  • Men and women, ages 18 years and up
  • English speaking
  • Military Veterans

Exclusion criteria

  • Those with a contraindication for MRIs (e.g. implanted metal)
  • History of head trauma with loss of consciousness
  • History of seizures or on medications that substantially reduce seizure threshold
  • Neurological or uncontrolled medical disease
  • Active substance abuse
  • Currently pregnant or breastfeeding

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Crossover
Masking
Double blind
Primary purpose
Basic science

Study locations

United States · 1 center
  • VA Palo Alto Health Care System, Palo Alto, CA — Palo Alto

Identifiers

NCT: NCT06548113 · MHBC-011-24F · 76106

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗