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The A-LIST WMM Insights Series

U

UsAgainstAlzheimer's

Status

Enrolling

Conditions

Alzheimer Disease
Mild Cognitive Impairment
Dementia

Study type

Observational

Funder types

Other

Identifiers

NCT04466722
A-LIST Protocol 1

Details and patient eligibility

About

The main purpose of the Study is to develop an understanding over time and through multiple research projects, including surveys, interviews, online focus groups, and other primary research methodologies (A-LIST Research Projects) on what matters most to individuals concerned about brain health and those with and/or affected by Alzheimer's disease and other dementias, including caregivers.

Full description

To do this, UsAgainstAlzheimer's will identify and engage individuals who want to focus on brain health; individuals who are worried about their cognition; individuals who perceive themselves to be at risk for Alzheimer's disease (AD); individuals who may be at risk for AD due to self-identified confirmation of underlying disease pathology; individuals who self-identify as having a diagnosis of mild cognitive impairment (MCI) or of AD or another dementia; and those who self-identify as current or former caregivers of patients with Alzheimer's disease or another dementia to participate in the A-LIST Research Projects. Such participants will either already be - or will be invited to become - members of the A-LIST cohort, an online cohort of individuals ready and willing to engage in A-LIST WMM Insights Series (A-LIST members).

The A-LIST WMM Insights Series will enlist participants to offer insights into a range of issues relevant to Alzheimer's, including as examples issues pertinent to clinical trial design, regulatory submissions, other research strategies, payer value determinations, and care and services research. The A-LIST WMM Insights Series may seek information that in some instances will be marketing research or other research exempt from IRB oversight. However, when an individual A-LIST Research Project constitutes human subjects research consistent with governing law, IRB approval will be sought and obtained. Where questions exist whether an individual A-LIST Research Project constitutes human subject research, IRB determination will be solicited.

Enrollment

10,000 estimated patients

Sex

All

Ages

18 to 100 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

To be eligible to participate in the Study, an individual must meet all of the following criteria:

  1. Age 18 years or older.
  2. United States, Canada resident.
  3. Self-report of cognitive difficulties, caregiver status or interest in brain health.
  4. Have indicated willingness to participate by selecting "I Agree" option when joining the A-LIST. Additionally, will have clicked on link - invitation to take a specific survey
  5. Able to speak, read, and understand English.

Exclusion criteria

An individual who meets any of the following criteria will be excluded from participation in this Study:

  1. Unable to comply with the Study requirements.

Trial contacts and locations

1

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Central trial contact

Virginia Biggar, BA; Theresa Frangiosa, MBA

Data sourced from clinicaltrials.gov

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