Houston, TXNCT06723743Now EnrollingIRB Ready

Traumatic Brain Injury (TBI) Patients Clinical Trial in Houston, TX

Access cutting-edge traumatic brain injury (tbi) patients treatment through this clinical trial at a research site in Houston. Study-provided care at no cost to qualified participants.

Sponsored by Baylor College of Medicine

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Expert Care in Houston

Access traumatic brain injury (tbi) patients specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related traumatic brain injury (tbi) patients treatment provided free

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Check if you qualify for this traumatic brain injury (tbi) patients clinical trial in Houston, TX

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Why Participate?

  • No-Cost Study Care

  • Local to Houston

    Convenient for TX residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Houston site if eligible
  4. 4Begin participation

About This Traumatic Brain Injury (TBI) Patients Study in Houston

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.

Sponsor: Baylor College of Medicine

Who Can Participate

Inclusion Criteria

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

Exclusion Criteria

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
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

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Houston?

Yes, this clinical trial (NCT06723743) has an active research site in Houston, TX that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Traumatic Brain Injury (TBI) Patients Treatment Options in Houston, TX

If you're searching for traumatic brain injury (tbi) patients treatment options in Houston, TX, this clinical trial (NCT06723743) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Houston research site is actively enrolling participants for this clinical trial. You'll receive care from experienced traumatic brain injury (tbi) patients specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all traumatic brain injury (tbi) patients clinical trials near you to find additional studies recruiting in your area.

More Traumatic Brain Injury Trials in Houston, TX

See all traumatic brain injury clinical trials recruiting in Houston — not just this study.

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