Advisory Council February 2017 Meeting Presentation: Development and Use of Registries



Friday, February 3, 2017

Printer Friendly Version in PDF Format (9 PDF pages)


Development and use of registries to accelerate enrollment into Alzheimer's trials

Jessica B. Langbaum, PhD
Principal Scientist, Banner Alzheimer's Institute
Associate Director, Alzheimer's Prevention Initiative

Current Landscape in the United States

  • In 2014, ~70,000 participants need to fill 150 Alzheimer's disease (AD) trials
    • Requires screening minimum 10x as many participants
  • Anticipate a rapid upturn in the number of AD trials in the coming years
    • Particularly in hard to recruit populations (healthy older adults at risk for AD, MCI, mild/prodromal AD patients)
  • At the same time, recruitment for trials face obstacles, approximately:
    • 85-90% of all studies have delays in recruitment
    • 30% of studies under enroll
    • Only 7% of studies meet enrollment goals in the originally stated timelines
    • Under enrollment of African Americans & Hispanic/Latinos in studies limiting generalizability of trial findings

Why a Registry?

  • Ability to have thousands of interested individuals available to be contacted for a given study
    • GAP has estimated ~7 million adults need to be contacted in order to enroll 4,500 participants!
  • Potential to reduce screen fail rate
  • Potential to accelerate enrollment into trial, perhaps enhance retention of trial participants
  • Online registry can complement and enhance local, grassroots recruitment effort and may be more cost-effective / efficient
  • Depending on registry's design, may be able to leverage run-in data for trial

Challenges to Developing Recruitment Registries -- Just the tip of the iceberg!

  • If you build it, it does not necessarily mean they will come!
    • Why join if you are healthy?
    • And those who do join are predominately white, educated & female. Lack of "best practices"
    • how much data do you collect at signup? Different thresholds of commitment at entry yield different populations, results.
  • Requires a high level of customer service and continued engagement
    • Reason why API is still only in English
  • Ethics committee / IRB constraints and HIPAA constraints for sharing participant information with enrolling studies/sponsors APR is creating "StudyMatch" platform
    • Complicated legal landscape in the US when DNA collection is added
  • Creating IT infrastructure is time consuming and expensive; no perfect "out of the box" solution
  • Model in US may need adaptation for ex-US
  • Funding

Motivators and Barriers to Joining a Registry

  • We conducted a national survey in 2012 (1024 US adults) and in 2014/15 analyzed nearly 19,000 conversations from 84 online destinations to try to understand the primary motivators and barriers for joining a registry and participating in trial
    • High interest in learning more about registries
    • Drivers include helping future generations, driving science forward, taking control of their own lives
    • Barriers include concerns regarding privacy/confidentiality, data security, who is "behind" the program

Alzheimer's Prevention Registry

  • Who
    • Anyone age 18 and older
  • Where
    • Anywhere in the world; initial outreach has been focused in the United States
  • What & How
    • Provide email address, other demographic & contact information at sign up
    • Information is kept confidential and secure
    • Receive emails with study opportunities, research news Website

Alzheimer's Prevention Registry Home Page screen shot.

Enrollee Demographics

  • As of January 15, 2017 more than 255,000 enrolled
    • 81% of enrollees are female
    • 70% self-report a family history of Alzheimer's or other dementia
    • 90% self-report not having a diagnosis of a cognitive impairment
Bar Chart.

Alzheimer's Prevention Registry

How much information are people willing to give about themselves?

And can we use that information to help match them to studies?

GeneMatch: A new program of the Alzheimer's Prevention Registry

GeneMatch: A program of the Alzheimer's Prevention Registry

  • Participants sign up on the website (
    • Review brief, online education module (video or bulleted text)
    • Create a GeneMatch account
    • Electronically sign an informed consent
    • Provide demographic information
  • Participants receive a cheek swab kit in the mail approximately 2 weeks later
  • Participants complete the cheek swab at home and send it back in a pre-paid postage envelope along with the laboratory requisition form to the lab
  • CLIA-certified lab analyzes the swab and genetic information is stored in a secure database not viewed or accessed by GeneMatch staff
  • GeneMatch does NOT disclose genotype results to participants
    • APOE genotype is used to help match people to study opportunities

GeneMatch Partner Sites

  • Numerous Generation Study Sites are GeneMatch partner sites (aka, performance sites)
    • Requires institution to approve WIRB as IRB of record and site investigator as program sub-I
    • Not all institutions are willing to opt-in, with varying points of resistance
    • Allows for buccal swab kits to be distributed and completed on-site
    • Benefits:
      • Reduces time between enrollment and when APOE results are in the database
      • Allows sites to boost GeneMatch enrollment in their catchment area

GeneMatch Metrics

  • 31,149 enrolled as of January 24, 2017
  • GeneMatch Participant Demographics:
    • 70% female
    • ~4-5% APOE 4/4
    • ~30% APOE 3/4
  • Promoting the API Generation Study to GeneMatch members:
    • 264 invited to the study
    • 123 accepted their invitation
    • 1 declined

GeneMatch -- Enrollment by State (as of 16-January 2017)

United States map.

Facebook Advertising: 2016 Success Story

  • Over 16,000 new GeneMatch members in Q4 2016
    • The result of targeted Facebook campaign
      • 21% of people who clicked on an ad completed the GeneMatch enrollment process
      • The most successful creative concepts were those that utilized social pressure and those that contained elements that have been shown to drive high click-through rates (i.e. polling boxes)
      • Average cost $2.88/enrolled

GeneMatch -- 2016 Advertising

Examples of GeneMatch Facebook Advertising screen shots.

Potential Solutions

  • Increase participation of underrepresented populations
    • Overhaul of content and messaging to ensure clear, accessible language
      • More approachable for low literacy English speakers, which will likely enhance usability for higher-literacy users
      • Translate content into other languages, starting with Spanish
  • Development of a repository for screen failed participants
    • Not sponsor specific
    • Contains reasons for screen fail (e.g., SUVR value amyloid positive) and ability to re-contact participants for other studies
  • National IRB oversight of registries, willingness to approve motivational (not overpromising) messaging. Examine HIPAA constraints and potential solutions
  • Federal funding for registries that provide a shared recruitment resource

Return to

National Alzheimer's Project Act Home Page

Advisory Council on Alzheimer's Research, Care, and Services Page

Advisory Council on Alzheimer's Research, Care, and Services Meetings Page