30 Participants Needed

Quest AD-Detect Blood Test for Alzheimer's Disease

Recruiting at 5 trial locations
CR
Overseen ByClinical Research Nurse Coordinator
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Covenant Health, US
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial examines whether a new blood test, called Quest AD-Detect, can help doctors diagnose Alzheimer's disease earlier in hospitalized patients with cognitive issues, such as confusion or memory problems. The goal is to determine if this test can distinguish between Alzheimer's and other causes of these issues. Participants will have a follow-up six months after leaving the hospital to discuss their results. Suitable candidates are those aged 60 to 90, currently hospitalized with cognitive problems, and without a prior dementia diagnosis. As an unphased study, this trial offers a unique opportunity to contribute to groundbreaking research that could enhance early diagnosis of Alzheimer's disease.

Will I have to stop taking my current medications?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.

What prior data suggests that the Quest AD-Detect blood test is safe?

Research has shown that the Quest AD-Detect blood test can accurately identify Alzheimer's disease, with over 90% accuracy in both detecting the disease and confirming its absence. The test assesses the risk of dementia, including Alzheimer's, without involving medication, eliminating concerns about drug side effects. However, like any test, there is a small chance of a false positive or false negative result. Overall, the test is considered safe and easy to use.12345

Why are researchers excited about this trial?

The Quest AD-Detect blood test is unique because it offers a non-invasive way to detect Alzheimer's disease compared to traditional methods like brain imaging and spinal taps, which can be uncomfortable and costly. Researchers are excited about this test because it aims to identify Alzheimer's earlier by detecting specific biomarkers in the blood, potentially allowing for earlier intervention and better management of the disease. This could revolutionize how Alzheimer's is diagnosed, making it more accessible and less burdensome for patients.

What evidence suggests that the Quest AD-Detect blood test is effective for diagnosing Alzheimer's disease?

Research has shown that the Quest AD-Detect blood test, provided to all eligible participants in this trial, accurately diagnoses Alzheimer's disease. Studies have found it correctly identifies Alzheimer's in 91% of cases and accurately rules it out in 91% of people without the disease. The test detects specific proteins in the blood, called amyloid-beta, linked to Alzheimer's. By tracking changes in these proteins, the test helps assess the risk of developing the disease. These findings suggest that the Quest AD-Detect blood test effectively distinguishes Alzheimer's from other memory and thinking problems.45678

Who Is on the Research Team?

SM

Samuel Moore, MD

Principal Investigator

Covenant Health, Canada

Are You a Good Fit for This Trial?

This trial is for hospitalized patients experiencing cognitive issues like delirium or encephalopathy, who may have an underlying Alzheimer's disease. The study aims to identify those with Alzheimer's early on using a blood test.

Inclusion Criteria

No prior diagnosis of dementia
I am between 60 and 90 years old.
I am in the hospital due to a brain condition caused by toxins or metabolic issues.

Exclusion Criteria

Prior diagnosis of dementing illness or other organic etiology to cognitive impairment
I am younger than 60 years old.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

1-2 weeks

Inpatient Testing

Participants receive the Quest AD-Detect blood test while hospitalized for cognitive diagnosis

During hospitalization
Inpatient visit

Follow-up

Neurology Clinic completes a 6-month post-hospitalization follow-up to discuss the risk assessment portfolio

6 months
1 visit (in-person)

What Are the Treatments Tested in This Trial?

Interventions

  • Quest AD-Detect blood test
Trial Overview The Quest AD-Detect blood test is being tested to see if it can differentiate between Alzheimer's disease and other cognitive impairments in hospitalized patients, followed by a neurology clinic assessment after six months.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: All eligible patients will receive a Quest AD-Detect blood testExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Covenant Health, US

Lead Sponsor

Citations

New Study Demonstrates Accuracy of Two Quest AD- ...Both tests were evaluated at 91% sensitivity and 91% specificity to meet acceptable performance of confirmatory blood biomarker tests in an ...
Quest Diagnostics Launches New AD-Detect™ Blood Test ...The test can accurately assess Alzheimer's disease pathology with greater than 90% sensitivity and specificity.
New Study Demonstrates Accuracy of Two Quest AD- ...Both tests were evaluated at 91% sensitivity and 91% specificity to meet acceptable performance of confirmatory blood biomarker tests in an ...
Assessing Alzheimer's risk starts with a single blood testThe QUEST AD-Detect Amyloid Beta 42/40 Ratio is designed to monitor Aβ 42/40 changes over time to help assess the risk potential of Alzheimer's disease.
Current Screening Tests/Biomarkers for Alzheimer's DiseaseQuest Diagnostics released the AD-Detect™ Test on July 31, 2023, a direct-to-consumer plasma-based biomarker test for AD that measures amyloid-beta 42 and ...
Quest Diagnostics Launches New AD-Detect™ Blood Test ...The test can accurately assess Alzheimer's disease pathology with greater than 90% sensitivity and specificity.
Dementia TestingQuest AD-Detect is a portfolio of blood-based risk assessment offerings that can help provide better understanding of a patient's potential risk for dementia ...
FDA Clears First Blood Test Used in Diagnosing ...The risks associated with the Lumipulse G pTau217/ß-Amyloid 1-42 Plasma Ratio are mainly the possibility of false positive and false negative ...
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