Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
200000 participants
OBSERVATIONAL
2017-12-20
2026-04-30
Brief Summary
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Detailed Description
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Individuals who join the APT Webstudy will register at https://www.aptwebstudy.org/, sign an electronic informed consent form (ICF), provide basic demographic information and participate in web-based cognitive testing. Participants will return the APT Webstudy quarterly (every 3 months) to complete the cognitive testing again.
Based on the risk score and changes identified in the cognitive testing results, participants will be invited to visit a partnering clinical trial site for an in-person visit with biomarker testing and clinical assessment.
The combined results of the web-based assessments, with the biomarker and clinical assessments, will allow an adaptive statistical algorithm to improve the selection of those at highest risk for developing AD.
To Join the APT Webstudy, please visit https://www.aptwebstudy.org/.
Conditions
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Study Design
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OTHER
OTHER
Eligibility Criteria
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Inclusion Criteria
* no evidence of dementia
* willing to participate in remote longitudinal cognitive testing and possible referral for biomarker assessment based on risk
Exclusion Criteria
50 Years
85 Years
ALL
Yes
Sponsors
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National Institute on Aging (NIA)
NIH
Brigham and Women's Hospital
OTHER
The Cleveland Clinic
OTHER
University of Southern California
OTHER
Responsible Party
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Paul S. Aisen
Professor
Principal Investigators
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Paul Aisen, MD
Role: PRINCIPAL_INVESTIGATOR
USC ATRI
Reisa Sperling, MD
Role: PRINCIPAL_INVESTIGATOR
Brigham and Women's Hospital
Jeffrey Cummings, MD
Role: PRINCIPAL_INVESTIGATOR
The Cleveland Clinic
Locations
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Https://Www.Aptwebstudy.Org
San Diego, California, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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HS-17-00746
Identifier Type: -
Identifier Source: org_study_id
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