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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03944603
Other study ID # 18-2607
Secondary ID R01AG058772
Status Active, not recruiting
Phase
First received
Last updated
Start date April 30, 2019
Est. completion date March 31, 2025

Study information

Verified date April 2024
Source University of Colorado, Denver
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study plans to examine biological bases of cognitive aging. The goals of the study are to better understand how immune system markers, measured in the blood and in the spinal fluid, are related to clinical features of aging over time. The study also aims to better understand how different types of biomarkers may relate to immune health and the aging process. This research may ultimately help us better understand what puts individuals at risk for cognitive decline and for Alzheimer's disease.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 300
Est. completion date March 31, 2025
Est. primary completion date March 31, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 60 Years to 89 Years
Eligibility Inclusion Criteria: 1. Between ages of 60-89 2. Have a reliable study partner who has frequent contact with the subject (i.e., at least twice per month) and is able to provide information about functional abilities 3. Mini Mental State Examination (MMSE) >23 4. Clinical Dementia Rating (CDR) global score of 0 5. No informant report of significant cognitive decline in prior year 6. No evidence from the screening visit suggesting a neurodegenerative disorder (per team neurologist) 7. Willingness to complete both baseline and 2-year follow-up procedures Exclusion Criteria: 1. Major psychiatric disorder (e.g. schizophrenia, bipolar disorder, untreated major depression within past year) 2. Neurological conditions affecting cognition (e.g. Parkinson's disease, epilepsy (onset prior than 2 years ago), head trauma with loss of consciousness >5 min within past two years, large vessel infarct, mild cognitive impairment, or dementia) 3. CNS immune conditions and other conditions affecting cognition (e.g., multiple sclerosis, paraneoplastic encephalitides; Hashimoto's encephalopathy; systematic lupus erythematosus) 4. Systematic illness (e.g.,current cancer, renal failure, respiratory failure) 5. Substance abuse/dependence (DSM-V criteria) 6. Current medication use likely to affect CNS (e.g., long-acting benzodiazepines, neuroleptics in the phenothiazine and haloperidol families) 7. Current medication use that precludes lumbar punctures (e.g. anticoagulants, antiplatelets, heparin shots, or some other blood thinner medications: Warfarin [coumadin], Pradaxa [dabigatran], Xarelto [rivaroxaban]. Eliquis [apixaban], or Plavix [clopidogrel]. 8. Significant sensory or motor deficits that would interfere with cognitive testing 9. Factors that preclude MR imaging (e.g., pacemaker) 10. Factors that preclude lumbar puncture

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Colorado Anschutz Medical Campus Aurora Colorado

Sponsors (2)

Lead Sponsor Collaborator
University of Colorado, Denver National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Levels of Immune Protein Markers in Blood and CSF Outcome measures will include longitudinal changes in protein levels of blood inflammation and CSF inflammation 2-Year Changes
Primary Performance on Neuropsychological Measures Outcome measures will include longitudinal changes in cognitive measures (e.g., memory and executive functions) over time 2-Year Changes
Primary Levels of Exosomal Innate Immune Markers in Blood and CSF Outcome measures will include longitudinal changes in innate immune markers in exosomes (i.e., extracellular vesicles) 2-Year Changes
Secondary Brain Structure Outcome measures will include baseline structural brain imaging Baseline
Secondary CSF Levels of Alzheimer's Disease Related Markers Outcome measures will include CSF levels of proteins associated with Alzheimer's disease pathology 2-year change