Transcutaneous Vagus Nerve Stimulation for Attention and Memory

Recruiting now · Not applicable · Has a placebo group

Conditions studied: Traumatic Brain Injury (TBI) Patients

In brief

This clinical trial aims to evaluate whether transcutaneous auricular vagus nerve stimulation (taVNS), a non-invasive brain stimulation method, can improve attention and memory in veterans with traumatic brain injury (TBI) and depression and/or posttraumatic stress disorder (PTSD). The study seeks to answer two main questions: 1. Can active taVNS improve attention and memory compared to sham (placebo) stimulation? 2. Does taVNS affect heart rate variability (HRV)? taVNS delivers a gentle electrical current to the vagus nerve through electrodes placed on the ear, targeting brain areas involved in attention and memory without requiring surgery. This study uses a crossover design, meaning all participants will experience two sessions: one with active taVNS and one with sham stimulation. The sham session feels similar but does not deliver actual stimulation, allowing researchers to compare the two and understand taVNS's effects on the brain. In a single visit, participants will: * Complete eligibility screening (questionnaires and vital signs). * Undergo two sessions (one active and one sham), randomly assigned. * Perform attention tasks before and after each session. * Have their heart rate monitored during the sessions. The findings will help determine whether taVNS could be an effective treatment for improving attention and memory in veterans with TBI.

Key facts

Study ID

NCT06723743

Run by

Baylor College of Medicine

People needed

30

Starts

2026-08-01

Expected to finish

2027-08-01

Last updated by the study team

2026-05-07

Who can join

Age: 25 and older, up to 64. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Ages 25-64
• Right-handedness
• Veterans with a history of deployment to Operation Iraqi Freedom (OIF), Operation Enduring Freedom (OEF), Operation New Dawn (OND) or other post 9/11 war on terrorism
• History of PTSD and/or depression
• Military related mild traumatic brain injury
• If taking psychotropic medication, demonstrate stability for 3 months
• If taking stimulants, washout period of 12 hours

You may not qualify if…

• History of neurological, cardiovascular, or pulmonary disease
• Cardiac arrhythmia (all types)
• Active suicidal ideation
• Visible wounds on skin of the left ear
• Medical implants such as cardiac defibrillators, pacemakers, or deep brain stimulators
• Pregnancy
• Completed taVNS in the past 4 weeks
• Current substance use disorder (exception: mild cannabis use disorder allowed)
• Current moderate or severe alcohol use disorder
• Major cognitive disorder

Where it is running

• Michael E. DeBakey VA Medical Center — Houston, Texas, United States (enrolling)
• Michael E. DeBakey VA Medical Center — Houston, Texas, United States (enrolling)

Full record on ClinicalTrials.gov

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