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Sensory Synchronized Imaging and Neuromodulation

Investigation of Sensory Synchronized Human Brain Imaging and Neuromodulation

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06548113
Enrollment
250
Registered
2024-08-12
Start date
2026-07-13
Completion date
2030-12-31
Last updated
2026-06-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Major Depressive Disorder

Brief summary

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

DEVICETMS

transcranial magnetic brain stimulation

Sponsors

VA Office of Research and Development
Lead SponsorFED
National Institute of Mental Health (NIMH)
CollaboratorNIH
Stanford University
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Transcranial Magnetic Stimulation (TMS) / Electroencephalography (EEG) change45 minutesChange in the TMS-EEG measure will be assessed before, during, and after each TMS session. Specifically, the difference in size of the evoked response after a single TMS pulse in the frontoparietal region will be quantified in microVolts and compared between standard TMS and sensory-entrained TMS (se-TMS).

Countries

United States

Contacts

CONTACTJessica M Ross, PhD
jessica.ross1@va.gov(530) 902-2450
PRINCIPAL_INVESTIGATORJessica M Ross, PhD

VA Palo Alto Health Care System, Palo Alto, CA

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 26, 2026