RecruitingNot ApplicableNCT07222280

Clinical Trial Protocol: Alzheimer's Dementia Underlying Encephalopathy


Sponsor

Covenant Health, US

Enrollment

30 participants

Start Date

Jun 10, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to determine if utilizing the Quest AD-Detect blood test, while patient's are hospitalized for a cognitive diagnosis (such as delirium or encephalopathy), will result in an earlier diagnosis of underlying Alzheimer's disease. * Will this blood test have the ability to distinguish between Alzheimer's disease and other causes of cognitive impairment in the inpatient setting? * Neurology Clinic will complete a 6-month post-hospitalization follow up with patients who have had the Quest AD-Detect Alzheimer's Disease blood test completed while they were inpatient to discuss the risk assessment portfolio


Eligibility

Min Age: 60 YearsMax Age: 90 Years

Inclusion Criteria3

  • Ages 60 to 90 years old
  • No prior diagnosis of dementia
  • Currently hospitalized with cognitive diagnosis, including but no limited to; delirium, encephalopathy, etc. thought to be secondary to a toxic/metabolic state

Exclusion Criteria2

  • Age under 60 years
  • Prior diagnosis of dementing illness or other organic etiology to cognitive impairment

Interventions

DIAGNOSTIC_TESTQuest AD-Detect blood test

Blood will be collected and sent for testing using the Quest AD-Detect blood test


Locations(6)

Cumberland Medical Center

Crossville, Tennessee, United States

Roane Medical Center

Harriman, Tennessee, United States

Fort Sanders Regional Medical Center

Knoxville, Tennessee, United States

Fort Loudon Medical Center

Lenoir City, Tennessee, United States

Methodist Medical Center

Oak Ridge, Tennessee, United States

LeConte Medical Center

Sevierville, Tennessee, United States

View Full Details on ClinicalTrials.gov

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NCT07222280


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