No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
30 – 90
Sex
Any
Study type
Observational
Participants needed
800 (estimated)
Sponsor
VA Office of Research and Development · Federal
Who this trial is looking for
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This is a research study that aims to examine whether Veterans with mild Traumatic Brain Injuries are at risk for dementia by studying their memory, brain wave activity, brain structure and proteins that can be elevated after brain injury and in dementia.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
All Subjects:
* Intact color vision
* Visual acuity of 20/30 (or better)
* Patients must pass effort measures on the TOMM
* Patients must have intact decision-making capacity
* Patients must have no contraindications to lumbar puncture including:
* Being on a blood thinner
* As…
Inclusion Criteria:
All Subjects:
* Intact color vision
* Visual acuity of 20/30 (or better)
* Patients must pass effort measures on the TOMM
* Patients must have intact decision-making capacity
* Patients must have no contraindications to lumbar puncture including:
* Being on a blood thinner
* Aspirin or Plavix
* Have no space occupying lesion on magnetic resonance imaging (MRI)
* An International Normalized Ratio (INR) value \< 1.4 and platelet count \>50,000
* No epidural infection or overlying cellulitis over the lumbar spine
* PTSD will be accounted for as a potential confounder and its presence will be included as a covariate in all analyses
Mild TBI Subjects:
* Subjects will be recruited who have a physician diagnosis of 1 or more mTBI episodes without concomitant moderate or severe TBI diagnosis
* Mild TBI: Loss of consciousness greater than 30 minutes, posttraumatic amnesia greater than 24 hours, and/or altered mental status greater than 24 hours
Moderate TBI Subjects:
* Subjects will be recruited who have a physician diagnosis of 1 or more moderate TBI episodes
* Moderate TBI: loss of consciousness greater than 30 minutes, posttraumatic amnesia greater than 24 hours, and altered mental status greater than 24 hours
MCI Subjects:
* Subjects will be recruited that meet diagnostic criteria for MCI (without a history of TBI) based on the judgement of a behavioral neurologist following the 2011 MCI criteria
* Specifically, subjects will test in the impaired range on one or more cognitive domains on neuropsychological testing and will not have impairments in function, i.e. will not meet diagnostic criteria for dementia
* Subjects with MCI may or may not meet diagnostic criteria for MCI due to AD
* MCI subjects will be matched for their MoCA score with older TBI subjects
Healthy Controls:
* Cognitively normal control subjects, age-, education- and sex-matched with mild TBI subjects, but lacking and TBI history
* All subjects must be within 1 standard deviation of normal on all neuropsychologic testing in order to be enrolled
The investigators will recruit all subjects without regard to gender, race, ethnicity, socioeconomic status, or other factors to allow results of this research to yield the greatest generalizability
Exclusion Criteria:
All Subjects:
* If the primary language is not English
* Are unable to understand the informed consent process
* Have a clinically significant problem with any of the following conditions:
* A history of TBI within 1 year of study
* Suicidal or homicidal ideation requiring intervention
* Schizophrenia
* Bipolar disorder
* Active alcohol or drug abuse
* Clinically significant neurological disease other than those stated in the inclusion criteria
* Impaired decision-making ability
* Patients will be excluded if there are contraindications to MRI including:
* Implants
* Shrapnel
* Aneurysm clips
* Pacemaker
* Pregnancy
* Non-TBI subjects must not have had an TBI
* No contraindication to lumbar puncture or blood draw including:
* Being on a blood thinner
* Aspirin or Plavix
* No space occupying lesion on MRI that makes lumbar puncture contraindicated
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