Alzheimer Prevention Trials (APT) Webstudy
2 other identifiers
observational
200,000
1 country
1
Brief Summary
The goal of the Alzheimer Prevention Trials (APT) Webstudy is to accelerate enrollment for Alzheimer's disease (AD) clinical trials by identifying and tracking individuals who may be at higher risk for developing AD dementia.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2017
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 20, 2017
CompletedFirst Submitted
Initial submission to the registry
August 16, 2018
CompletedFirst Posted
Study publicly available on registry
August 20, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2026
CompletedJuly 16, 2025
July 1, 2025
8.4 years
August 16, 2018
July 11, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Enrollment into Alzheimer's prevention research studies
5 years
Secondary Outcomes (2)
Referral into prevention research studies
5 years
Number of individuals enrolled into Alzheimer's prevention studies
5 years
Eligibility Criteria
Anyone who meets entry criteria is eligible to join the Webstudy. We anticipate 200,000 individuals will join.
You may qualify if:
- male or female at least 50 years of age
- no evidence of dementia
- willing to participate in remote longitudinal cognitive testing and possible referral for biomarker assessment based on risk
You may not qualify if:
- N/A. Anyone can register for the APT Webstudy, however, only individuals identified using the risk algorithm will be referred for in-person biomarker assessments.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Southern Californialead
- National Institute on Aging (NIA)collaborator
- Brigham and Women's Hospitalcollaborator
- The Cleveland Cliniccollaborator
Study Sites (1)
Https://Www.Aptwebstudy.Org
San Diego, California, 92121, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Paul Aisen, MD
USC ATRI
- PRINCIPAL INVESTIGATOR
Reisa Sperling, MD
Brigham and Women's Hospital
- PRINCIPAL INVESTIGATOR
Jeffrey Cummings, MD
The Cleveland Clinic
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- OTHER
- Target Duration
- 5 Years
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
August 16, 2018
First Posted
August 20, 2018
Study Start
December 20, 2017
Primary Completion
April 30, 2026
Study Completion
April 30, 2026
Last Updated
July 16, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share