Davos Alzheimer's Collaborative Study: Sequential Administration of Digital Testing To Screen For Cognitive Impairment Followed By Blood Based Biomarkers To Assist With Timely Detection And Accurate Diagnosis Of Alzheimer's Disease
Completed
Conditions studied: Alzheimer Disease
In brief
The purpose of this study is to investigate how we can detect Alzheimer's disease early by using an online memory test and a simple blood test. These new methods for early diagnosis could allow people to begin treatment sooner, with the potential to improve the lives of millions of people.
Key facts
- Study ID
- NCT05379348
- Run by
- AdventHealth Translational Research Institute
- People needed
- 1423
- Starts
- 2022-03-14
- Expected to finish
- 2025-08-05
- Last updated by the study team
- 2026-03-30
Who can join
Age: 65 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Subjects must meet the following criteria for entry into the study:
- Male or female > 65 years of age at the time of consent;
- Understand and voluntarily sign an informed consent form;
- Inclusion criteria is assessed at both e-consent (assessed by participant's self-reporting of age and understanding) and in-person consent at TRI (assessed by clinical research coordinators in TRI).
You may not qualify if…
- Subjects who meet any of the following criteria will not be eligible for entry into the study:
- Subjects who are unable to hear and see well enough to complete the assessments;
- Prior diagnosis of dementia or Alzheimer's disease documented in their medical record and/or as diagnosed by a physician; Exclusion criteria is assessed by by participant's self-reporting of understanding and not having a prior diagnosis of dementia at the time of e-consentand visit 1 at TRI. ).
Where it is running
- AdventHealth Translational Research Institute — Orlando, Florida, United States
Full record on ClinicalTrials.gov
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