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The Trial-Ready Cohort for Preclinical and Prodromal Alzheimer’s Disease (TRC-PAD): Experience from the First 3 Years
Background The Trial-Ready Cohort for Preclinical and Prodromal Alzheimer’s disease (TRC-PAD) aims to accelerate enrollment for Alzheimer’s disease (AD) clinical trials by remotely identifying and tracking individuals who are at high risk for developing symptoms of AD, and referring these individual...
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Published in: | The journal of prevention of Alzheimer's disease 2020, Vol.7 (4), p.234-241 |
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creator | Walter, S. Langford, O. G. Clanton, T. B. Jimenez-Maggiora, G. A. Raman, R. Rafii, M. S. Shaffer, E. J. Sperling, R. A. Cummings, J. L. Aisen, P. S. |
description | Background
The Trial-Ready Cohort for Preclinical and Prodromal Alzheimer’s disease (TRC-PAD) aims to accelerate enrollment for Alzheimer’s disease (AD) clinical trials by remotely identifying and tracking individuals who are at high risk for developing symptoms of AD, and referring these individuals to in-person cognitive and biomarker evaluation with the purpose of engaging them in clinical trials. A risk algorithm using statistical modeling to predict brain amyloidosis will be refined as TRC-PAD advances with a maturing data set.
Objectives
To provide a summary of the steps taken to build this Trial-Ready cohort (TRC) and share results of the first 3 years of enrollment into the program.
Design
Participants are remotely enrolled in the Alzheimer Prevention Trials (APT) Webstudy with quarterly assessments, and through an algorithm identified as potentially at high risk, referred to clinical sites for biomarker confirmation, and enrolled into the TRC.
Setting
Both an online study and in-clinic non-interventional cohort study.
Participants
APT Webstudy participants are aged 50 or older, with an interest in participation in AD therapeutic trials. TRC participants must have a study partner, stable medical condition, and elevated brain amyloid, as measured by amyloid positron emission tomography or cerebrospinal fluid analysis. Additional risk assessments include apolipoprotein E genotyping.
Measurements
In the APT Webstudy, participants complete the Cognitive Function Index and Cogstate Brief Battery. The TRC includes the Preclinical Alzheimer’s Cognitive Composite, comprised of the Free and Cued Selective Reminding Test, the Delayed Paragraph Recall score on the Logical Memory IIa test from the Wechsler Memory Scale, the Digit-Symbol Substitution test from the Wechsler Adult Intelligence Scale-Revised, and the Mini Mental State Examination total score (
1
).
Results
During the first 3 years of this program, the APT Webstudy has 30,650 consented participants, with 23 sites approved for in person screening, 112 participants have been referred for in-clinic screening visits with eighteen enrolled to the TRC. The majority of participants consented to APT Webstudy have a family history of AD (62%), identify as Caucasian (92.5%), have over twelve years of formal education (85%), and are women (73%). Follow up rates for the first quarterly assessment were 38.2% with 29.5% completing the follow up Cogstate Battery.
Conclusions
After successfully designing and imple |
doi_str_mv | 10.14283/jpad.2020.47 |
format | article |
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The Trial-Ready Cohort for Preclinical and Prodromal Alzheimer’s disease (TRC-PAD) aims to accelerate enrollment for Alzheimer’s disease (AD) clinical trials by remotely identifying and tracking individuals who are at high risk for developing symptoms of AD, and referring these individuals to in-person cognitive and biomarker evaluation with the purpose of engaging them in clinical trials. A risk algorithm using statistical modeling to predict brain amyloidosis will be refined as TRC-PAD advances with a maturing data set.
Objectives
To provide a summary of the steps taken to build this Trial-Ready cohort (TRC) and share results of the first 3 years of enrollment into the program.
Design
Participants are remotely enrolled in the Alzheimer Prevention Trials (APT) Webstudy with quarterly assessments, and through an algorithm identified as potentially at high risk, referred to clinical sites for biomarker confirmation, and enrolled into the TRC.
Setting
Both an online study and in-clinic non-interventional cohort study.
Participants
APT Webstudy participants are aged 50 or older, with an interest in participation in AD therapeutic trials. TRC participants must have a study partner, stable medical condition, and elevated brain amyloid, as measured by amyloid positron emission tomography or cerebrospinal fluid analysis. Additional risk assessments include apolipoprotein E genotyping.
Measurements
In the APT Webstudy, participants complete the Cognitive Function Index and Cogstate Brief Battery. The TRC includes the Preclinical Alzheimer’s Cognitive Composite, comprised of the Free and Cued Selective Reminding Test, the Delayed Paragraph Recall score on the Logical Memory IIa test from the Wechsler Memory Scale, the Digit-Symbol Substitution test from the Wechsler Adult Intelligence Scale-Revised, and the Mini Mental State Examination total score (
1
).
Results
During the first 3 years of this program, the APT Webstudy has 30,650 consented participants, with 23 sites approved for in person screening, 112 participants have been referred for in-clinic screening visits with eighteen enrolled to the TRC. The majority of participants consented to APT Webstudy have a family history of AD (62%), identify as Caucasian (92.5%), have over twelve years of formal education (85%), and are women (73%). Follow up rates for the first quarterly assessment were 38.2% with 29.5% completing the follow up Cogstate Battery.
Conclusions
After successfully designing and implementing this program, the study team’s priority is to improve diversity of participants both in the APT Webstudy and TRC, to continue enrollment into the TRC to our target of 2,000, and to improve longitudinal retention, while beginning the process of referring TRC participants into clinical trials.</description><identifier>ISSN: 2274-5807</identifier><identifier>EISSN: 2426-0266</identifier><identifier>DOI: 10.14283/jpad.2020.47</identifier><identifier>PMID: 32920625</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Geriatrics/Gerontology ; Medicine ; Medicine & Public Health ; Neurology ; Special Article</subject><ispartof>The journal of prevention of Alzheimer's disease, 2020, Vol.7 (4), p.234-241</ispartof><rights>The Author(s) 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c426t-986f154bbe5303069b1f81823a74e7c2f14ef341c7c29f2f6e2280620e4da1633</citedby><cites>FETCH-LOGICAL-c426t-986f154bbe5303069b1f81823a74e7c2f14ef341c7c29f2f6e2280620e4da1633</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32920625$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Walter, S.</creatorcontrib><creatorcontrib>Langford, O. G.</creatorcontrib><creatorcontrib>Clanton, T. B.</creatorcontrib><creatorcontrib>Jimenez-Maggiora, G. A.</creatorcontrib><creatorcontrib>Raman, R.</creatorcontrib><creatorcontrib>Rafii, M. S.</creatorcontrib><creatorcontrib>Shaffer, E. J.</creatorcontrib><creatorcontrib>Sperling, R. A.</creatorcontrib><creatorcontrib>Cummings, J. L.</creatorcontrib><creatorcontrib>Aisen, P. S.</creatorcontrib><title>The Trial-Ready Cohort for Preclinical and Prodromal Alzheimer’s Disease (TRC-PAD): Experience from the First 3 Years</title><title>The journal of prevention of Alzheimer's disease</title><addtitle>J Prev Alzheimers Dis</addtitle><addtitle>J Prev Alzheimers Dis</addtitle><description>Background
The Trial-Ready Cohort for Preclinical and Prodromal Alzheimer’s disease (TRC-PAD) aims to accelerate enrollment for Alzheimer’s disease (AD) clinical trials by remotely identifying and tracking individuals who are at high risk for developing symptoms of AD, and referring these individuals to in-person cognitive and biomarker evaluation with the purpose of engaging them in clinical trials. A risk algorithm using statistical modeling to predict brain amyloidosis will be refined as TRC-PAD advances with a maturing data set.
Objectives
To provide a summary of the steps taken to build this Trial-Ready cohort (TRC) and share results of the first 3 years of enrollment into the program.
Design
Participants are remotely enrolled in the Alzheimer Prevention Trials (APT) Webstudy with quarterly assessments, and through an algorithm identified as potentially at high risk, referred to clinical sites for biomarker confirmation, and enrolled into the TRC.
Setting
Both an online study and in-clinic non-interventional cohort study.
Participants
APT Webstudy participants are aged 50 or older, with an interest in participation in AD therapeutic trials. TRC participants must have a study partner, stable medical condition, and elevated brain amyloid, as measured by amyloid positron emission tomography or cerebrospinal fluid analysis. Additional risk assessments include apolipoprotein E genotyping.
Measurements
In the APT Webstudy, participants complete the Cognitive Function Index and Cogstate Brief Battery. The TRC includes the Preclinical Alzheimer’s Cognitive Composite, comprised of the Free and Cued Selective Reminding Test, the Delayed Paragraph Recall score on the Logical Memory IIa test from the Wechsler Memory Scale, the Digit-Symbol Substitution test from the Wechsler Adult Intelligence Scale-Revised, and the Mini Mental State Examination total score (
1
).
Results
During the first 3 years of this program, the APT Webstudy has 30,650 consented participants, with 23 sites approved for in person screening, 112 participants have been referred for in-clinic screening visits with eighteen enrolled to the TRC. The majority of participants consented to APT Webstudy have a family history of AD (62%), identify as Caucasian (92.5%), have over twelve years of formal education (85%), and are women (73%). Follow up rates for the first quarterly assessment were 38.2% with 29.5% completing the follow up Cogstate Battery.
Conclusions
After successfully designing and implementing this program, the study team’s priority is to improve diversity of participants both in the APT Webstudy and TRC, to continue enrollment into the TRC to our target of 2,000, and to improve longitudinal retention, while beginning the process of referring TRC participants into clinical trials.</description><subject>Geriatrics/Gerontology</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Neurology</subject><subject>Special Article</subject><issn>2274-5807</issn><issn>2426-0266</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNpVUU1P3DAQtaqigoBjr5WP9JCtPXbspAek1QItEhIIbQ89Wd5kzHqVxIudpaWn_o3-PX4J5qMITp7RPL83bx4hHzmbcAmV-LJa23YCDNhE6ndkBySogoFS73MNWhZlxfQ22U9pxRjjNVeirj6QbQE1MAXlDvk1XyKdR2-74hJte0tnYRniSF2I9CJi0_nBN7ajdmhzH9oY-txNuz9L9D3Gu7__Ej3yCW1CejC_nBUX06PPX-nx7zVGj0OD1OUvdMwqJz6mkQr6E21Me2TL2S7h_vO7S36cHM9n34uz82-ns-lZ0WQrY1FXyvFSLhZYCiaYqhfcVbwCYbVE3YDjEp2QvMl17cApBKiyM4aytdmt2CWHT7zrzaLHtsFhjLYz6-h7G29NsN68nQx-aa7CjdFa6bIqM8HBM0EM1xtMo-l9arDr7IBhkwzIvGg-bg0Z-um11ovI_2tnwOQJkPJouMJoVmETh-zfcGYeEzUPiZqHRI3U4h7IQpHy</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Walter, S.</creator><creator>Langford, O. G.</creator><creator>Clanton, T. B.</creator><creator>Jimenez-Maggiora, G. A.</creator><creator>Raman, R.</creator><creator>Rafii, M. S.</creator><creator>Shaffer, E. J.</creator><creator>Sperling, R. A.</creator><creator>Cummings, J. L.</creator><creator>Aisen, P. S.</creator><general>Springer International Publishing</general><scope>C6C</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>2020</creationdate><title>The Trial-Ready Cohort for Preclinical and Prodromal Alzheimer’s Disease (TRC-PAD): Experience from the First 3 Years</title><author>Walter, S. ; Langford, O. G. ; Clanton, T. B. ; Jimenez-Maggiora, G. A. ; Raman, R. ; Rafii, M. S. ; Shaffer, E. J. ; Sperling, R. A. ; Cummings, J. L. ; Aisen, P. S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-986f154bbe5303069b1f81823a74e7c2f14ef341c7c29f2f6e2280620e4da1633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Geriatrics/Gerontology</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Neurology</topic><topic>Special Article</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Walter, S.</creatorcontrib><creatorcontrib>Langford, O. G.</creatorcontrib><creatorcontrib>Clanton, T. B.</creatorcontrib><creatorcontrib>Jimenez-Maggiora, G. A.</creatorcontrib><creatorcontrib>Raman, R.</creatorcontrib><creatorcontrib>Rafii, M. S.</creatorcontrib><creatorcontrib>Shaffer, E. J.</creatorcontrib><creatorcontrib>Sperling, R. A.</creatorcontrib><creatorcontrib>Cummings, J. L.</creatorcontrib><creatorcontrib>Aisen, P. S.</creatorcontrib><collection>SpringerOpen</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The journal of prevention of Alzheimer's disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Walter, S.</au><au>Langford, O. G.</au><au>Clanton, T. B.</au><au>Jimenez-Maggiora, G. A.</au><au>Raman, R.</au><au>Rafii, M. S.</au><au>Shaffer, E. J.</au><au>Sperling, R. A.</au><au>Cummings, J. L.</au><au>Aisen, P. S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Trial-Ready Cohort for Preclinical and Prodromal Alzheimer’s Disease (TRC-PAD): Experience from the First 3 Years</atitle><jtitle>The journal of prevention of Alzheimer's disease</jtitle><stitle>J Prev Alzheimers Dis</stitle><addtitle>J Prev Alzheimers Dis</addtitle><date>2020</date><risdate>2020</risdate><volume>7</volume><issue>4</issue><spage>234</spage><epage>241</epage><pages>234-241</pages><issn>2274-5807</issn><eissn>2426-0266</eissn><abstract>Background
The Trial-Ready Cohort for Preclinical and Prodromal Alzheimer’s disease (TRC-PAD) aims to accelerate enrollment for Alzheimer’s disease (AD) clinical trials by remotely identifying and tracking individuals who are at high risk for developing symptoms of AD, and referring these individuals to in-person cognitive and biomarker evaluation with the purpose of engaging them in clinical trials. A risk algorithm using statistical modeling to predict brain amyloidosis will be refined as TRC-PAD advances with a maturing data set.
Objectives
To provide a summary of the steps taken to build this Trial-Ready cohort (TRC) and share results of the first 3 years of enrollment into the program.
Design
Participants are remotely enrolled in the Alzheimer Prevention Trials (APT) Webstudy with quarterly assessments, and through an algorithm identified as potentially at high risk, referred to clinical sites for biomarker confirmation, and enrolled into the TRC.
Setting
Both an online study and in-clinic non-interventional cohort study.
Participants
APT Webstudy participants are aged 50 or older, with an interest in participation in AD therapeutic trials. TRC participants must have a study partner, stable medical condition, and elevated brain amyloid, as measured by amyloid positron emission tomography or cerebrospinal fluid analysis. Additional risk assessments include apolipoprotein E genotyping.
Measurements
In the APT Webstudy, participants complete the Cognitive Function Index and Cogstate Brief Battery. The TRC includes the Preclinical Alzheimer’s Cognitive Composite, comprised of the Free and Cued Selective Reminding Test, the Delayed Paragraph Recall score on the Logical Memory IIa test from the Wechsler Memory Scale, the Digit-Symbol Substitution test from the Wechsler Adult Intelligence Scale-Revised, and the Mini Mental State Examination total score (
1
).
Results
During the first 3 years of this program, the APT Webstudy has 30,650 consented participants, with 23 sites approved for in person screening, 112 participants have been referred for in-clinic screening visits with eighteen enrolled to the TRC. The majority of participants consented to APT Webstudy have a family history of AD (62%), identify as Caucasian (92.5%), have over twelve years of formal education (85%), and are women (73%). Follow up rates for the first quarterly assessment were 38.2% with 29.5% completing the follow up Cogstate Battery.
Conclusions
After successfully designing and implementing this program, the study team’s priority is to improve diversity of participants both in the APT Webstudy and TRC, to continue enrollment into the TRC to our target of 2,000, and to improve longitudinal retention, while beginning the process of referring TRC participants into clinical trials.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>32920625</pmid><doi>10.14283/jpad.2020.47</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Geriatrics/Gerontology Medicine Medicine & Public Health Neurology Special Article |
title | The Trial-Ready Cohort for Preclinical and Prodromal Alzheimer’s Disease (TRC-PAD): Experience from the First 3 Years |
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