Sensory Synchronized Imaging and Neuromodulation
Part of paid clinical trials in Palo Alto, California.
- Sponsor
- VA Office of Research and Development
- Study ID
- NCT06548113
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- TMS — DEVICEtranscranial magnetic brain stimulation
Study Details
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).
Key Dates
- Start date
- Jun 1, 2026
- Status verified
- May 2026
- Primary completion
- Oct 1, 2029
- Completion
- Oct 1, 2029
Study Design
- Enrollment
- 250 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- CROSSOVER
- Primary purpose
- BASIC_SCIENCE
Arms
- Active Comparator: Standard TMSA series of standard TMS protocols will be delivered to determine target engagement compared to seTMS. TMS will be delivered using neuro-navigation based on participant's own MRI images. Intensity will be set to 120% of the participant's motor threshold. Participants will be monitored during the session for adverse events and/or side effects.
- Active Comparator: Sensory-entrained TMS (seTMS)Sensory entrained TMS (seTMS) is a combination of music and TMS to align brain oscillations and enhance the effects of TMS. seTMS will be delivered to determine target engagement to noninvasive seTMS brain stimulation compared to standard TMS. TMS will be delivered using neuro-navigation based on participant's own MRI images. Intensity will be set to 120% of the participant's motor threshold. Participants will be monitored during the session for adverse events and/or side effects.
Primary Outcome Measure
Transcranial Magnetic Stimulation (TMS) / Electroencephalography (EEG) change [ Time Frame: 45 minutes ]
Central Contacts
- Jessica M Ross, PhD(530) 902-2450
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| VA Palo Alto Health Care System, Palo Alto, CA | Palo Alto | California | 94304-1207 | Jessica M Ross, PhD (PRINCIPAL_INVESTIGATOR) |
Find similar trials in Palo Alto, CA
Related Studies
- A Phase I/II Study of PDC-1421 for Treating Depression in Cancer PatientsPHASE1/PHASE2 · Not Yet Recruiting · BioLite, Inc. · Los Angeles, California
- Closed-Loop Deep Brain Stimulation for Major DepressionRecruiting · Andrew Krystal · San Francisco, California
- Spectral TMS (s-TMS)Enrolling By Invitation · University of California, Los Angeles · Los Angeles, California
- Biomarker-guided rTMS for Treatment Resistant DepressionPHASE3 · Recruiting · Weill Medical College of Cornell University · Stanford, California