Actively Recruiting

Age: 18Years - 74Years
All Genders
NCT06034509

Cognitive and Vascular Functioning Following TBI

Led by Walter Reed National Military Medical Center · Updated on 2025-09-26

300

Participants Needed

1

Research Sites

178 weeks

Total Duration

On this page

Sponsors

W

Walter Reed National Military Medical Center

Lead Sponsor

J

Johns Hopkins University

Collaborating Sponsor

AI-Summary

What this Trial Is About

This observational study will examine the association of chronic traumatic cerebrovascular injury and cardiovascular risk factors with TBI-related cognitive impairment and vascular dementia. Cerebrovascular, inflammatory, and neurodegenerative blood biomarkers as well as clinical and neuroimaging data

CONDITIONS

Official Title

Cognitive and Vascular Functioning Following TBI

Who Can Participate

Age: 18Years - 74Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Active duty Service Member or Veteran currently eligible for treatment at WRNMMC
  • Ability to read, write, and speak English
  • Ability to provide informed consent
  • Participation in NICoE Intensive Outpatient Program or NatHx Study comprehensive evaluation at least 3 years prior with valid neuropsychological test results
  • Consent to access prior research data and at least one prior blood specimen from NICoE, NatHx Study, or DoD Serum Biorepository
  • History of at least one mild, moderate, severe, or penetrating TBI more than 3 years ago, confirmed by loss of consciousness, post-traumatic amnesia, alteration of consciousness, neurologic dysfunction, or TBI-related abnormality on brain imaging
  • For additional control groups: history of military deployment with low blast exposure (<10 blasts) or significant blast exposure (≥10 blasts)
Not Eligible

You will not qualify if you...

  • Disabling neurological or psychological disorders such as autism, cerebral palsy, developmental disorder, stroke, brain tumor, multiple sclerosis, meningitis, encephalitis, brain abscess, vascular malformation, pre-injury epilepsy, schizophrenia, bipolar disorder, or personality disorder
  • Diabetes requiring drug treatment
  • Hypertension requiring more than one antihypertensive medication
  • History of myocardial infarction or other systemic vascular diseases
  • Diagnosis of dementia at initial NICoE or NatHx Study assessment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Walter Reed National Military Medical Center

Bethesda, Maryland, United States, 20889

Actively Recruiting

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Research Team

S

Sara M Lippa, PhD

CONTACT

M

Megan E Glazer, M.S.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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