Alzheimer Prevention Trials (APT) Webstudy
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Alzheimer Disease
- Sponsor
- University of Southern California
- Enrollment
- 200000
- Locations
- 1
- Primary Endpoint
- Enrollment into Alzheimer's prevention research studies
- Status
- Recruiting
- Last Updated
- 9 months ago
Overview
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.
Detailed Description
The APT Webstudy will use web-based cognitive testing and questionnaires to generate a risk score which will be used to identify individuals who may be at an increased risk for developing AD dementia. 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/.
Investigators
Paul S. Aisen
Professor
University of Southern California
Eligibility Criteria
Inclusion Criteria
- •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
Exclusion Criteria
- •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.
Outcomes
Primary Outcomes
Enrollment into Alzheimer's prevention research studies
Time Frame: 5 years
Secondary Outcomes
- Referral into prevention research studies(5 years)
- Number of individuals enrolled into Alzheimer's prevention studies(5 years)