Fort Lewis, WANCT05663034Now EnrollingIRB Ready

Traumatic Brain Injury Clinical Trial in Fort Lewis, WA

Access cutting-edge traumatic brain injury treatment through this clinical trial at a research site in Fort Lewis. Study-provided care at no cost to qualified participants.

Sponsored by Johns Hopkins University

Quick Self-Assessment

See if you qualify for this Fort Lewis location

Preparing your pre-screening questions…

Expert Care in Fort Lewis

Access traumatic brain injury specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related traumatic brain injury treatment provided free

Apply for This Fort Lewis Location

Check if you qualify for this traumatic brain injury clinical trial in Fort Lewis, WA

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Fort Lewis

    Convenient for WA 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 Fort Lewis site if eligible
  4. 4Begin participation

About This Traumatic Brain Injury Study in Fort Lewis

This study is a prospective two-arm, single blind randomized controlled trial design to compare the clinical effectiveness of telemedicine-delivered, 6-session, standardized cognitive behavioral therapy for insomnia (CBT-I) and mindfulness-based treatment for insomnia (MBTI) in treating insomnia symptoms and ameliorating depressive symptoms in persons with mild to moderate TBI and comorbid Post-Traumatic Stress Symptoms (PTSS) and insomnia symptoms in a 360 patients. Participants will undergo assessment (psychosocial questionnaires, neurocognitive testing, sleep monitoring) at baseline, at the end of treatment, and at 2-, 6- and 12-weeks post-treatment. The primary outcome is sleep as measured by the Insomnia Severity Index (ISI).

Sponsor: Johns Hopkins University

Who Can Participate

Inclusion Criteria

Current or former member of the uniform services
Meet the Veterans Affairs Medical Center (VAMC) Department of Defense (DoD) criteria for TBI;
Time duration since traumatic brain injury (TBI) injury \>90 days
Insomnia symptom duration \>90 days
Endorse insomnia symptoms (Insomnia Severity Index \[ISI\] score \> 10)
Display sufficient cognitive capacity to provide informed consent (Montreal Cognitive Assessment (MoCA) Z-score \> -2)
\>18 years of age
Access to and ability and to use computer.

Exclusion Criteria

History of neurological diseases other than TBI and not attributable to TBI
Sleep apnea \[apnea hypopnea index (AHI) \>15; individuals with mild apnea (AHI \> 5 and \<15) will be informed, but allowed to participate\]. Participants who use a continuous positive airway pressure (CPAP) device for sleep apnea will be eligible for participation if they are below the apnea/hypopnea cutoff while using CPAP, are adherent to using the device (\> 4 hours/night 21/30 consecutive days) and agree to continue using the device during study participation.
Lastly, people using psychotropic medications may be included if they are on a stable dosage for the last three weeks prior to the study.

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 Fort Lewis?

Yes, this clinical trial (NCT05663034) has an active research site in Fort Lewis, WA 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 Treatment Options in Fort Lewis, WA

If you're searching for traumatic brain injury treatment options in Fort Lewis, WA, this clinical trial (NCT05663034) 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 Fort Lewis research site is actively enrolling participants for this clinical trial. You'll receive care from experienced traumatic brain injury 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 clinical trials near you to find additional studies recruiting in your area.

More Traumatic Brain Injury Trials in Fort Lewis, WA

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

Browse Traumatic Brain Injury Trials in Fort Lewis →

Ready to Join in Fort Lewis?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Fort Lewis, WA