U24TR004437
Cooperative Agreement
Overview
Grant Description
Engaging Cooperative Sites for Trial Acceleration, Trust, Innovation, and Capability (ECSTATIC) - Clinical research comes in many different shapes and sizes, and a robust network must accommodate all trial types. No single organization can do this work alone. We have a deep commitment to both trial innovation and collective network capacity within and beyond the CTSA Consortium and have a lengthy history of supporting this approach.
We have demonstrated an exceptional ability to collaboratively innovate and share tools supporting clinical research coordination, including: global data management, mobile data collection, recruitment, electronic health record (EHR) research, single IRB coordination, contracting, community engagement, returning value to participants, eConsent, virtual/remote participation in studies, and EHR integration with REDCap. We will leverage and expand upon these programs as we are engaging cooperative sites for trial acceleration, trust, innovation, and capability (ECSTATIC).
We will establish a distributed alliance of 6 CTSA-aligned coordinating centers to add elastic capacity and broaden expertise to the TIN's CCC/DCC infrastructure. Our alliance has 14 expert trialists that can inform the use of integrated approaches for more efficient clinical research. Additionally, we will partner with the well-established Biostatistics, Epidemiology, and Research Design (BERD) group and health equity experts to ensure every study has access to needed expertise starting from study design through analysis.
We will broaden the types of organizations that can readily participate in clinical research across the U.S., including historically black colleges and universities (HBCUs), to reach the populations most in need of support. Based on our novel structure, merging teams from six different coordinating center groups, our TIC's capacity is both scalable and matched by expertise to intentionally accommodate all study design types.
Led by Gordon Bernard, MD, Wesley Self, MD, and Christopher Lindsell, PhD, each seasoned in leading and collaborating with multisite clinical trial networks, ECSTATIC will embrace and draw on diverse expertise to build, test, and share new resources that will enhance and accelerate rigorous, reproducible research for all CTSAs, to more rapidly improve human health.
Our specific aims are to:
1) Demonstrate and disseminate novel integrated approaches for more efficient clinical research including EHR-embedded, remote no-touch, and platform trials, aligning with study needs;
2) Expand and enrich clinical trial capability by increasing potential participating site expression of interest (EOI) reach and readiness support (HBCUs and rural practice-based research networks), better process integration with CTSAs, preparing study teams, and broader expert engagement;
3) Innovate clinical trial methodology by creating, evaluating, and disseminating new methods for risk monitoring, AE reporting, direct EHR to REDCap data capture, and data standards to all CTSAs; and
4) Provide a distributed alliance of clinical and data coordinating centers with extensive and diverse expertise to offer support tailored for trial design, population, and condition.
We have demonstrated an exceptional ability to collaboratively innovate and share tools supporting clinical research coordination, including: global data management, mobile data collection, recruitment, electronic health record (EHR) research, single IRB coordination, contracting, community engagement, returning value to participants, eConsent, virtual/remote participation in studies, and EHR integration with REDCap. We will leverage and expand upon these programs as we are engaging cooperative sites for trial acceleration, trust, innovation, and capability (ECSTATIC).
We will establish a distributed alliance of 6 CTSA-aligned coordinating centers to add elastic capacity and broaden expertise to the TIN's CCC/DCC infrastructure. Our alliance has 14 expert trialists that can inform the use of integrated approaches for more efficient clinical research. Additionally, we will partner with the well-established Biostatistics, Epidemiology, and Research Design (BERD) group and health equity experts to ensure every study has access to needed expertise starting from study design through analysis.
We will broaden the types of organizations that can readily participate in clinical research across the U.S., including historically black colleges and universities (HBCUs), to reach the populations most in need of support. Based on our novel structure, merging teams from six different coordinating center groups, our TIC's capacity is both scalable and matched by expertise to intentionally accommodate all study design types.
Led by Gordon Bernard, MD, Wesley Self, MD, and Christopher Lindsell, PhD, each seasoned in leading and collaborating with multisite clinical trial networks, ECSTATIC will embrace and draw on diverse expertise to build, test, and share new resources that will enhance and accelerate rigorous, reproducible research for all CTSAs, to more rapidly improve human health.
Our specific aims are to:
1) Demonstrate and disseminate novel integrated approaches for more efficient clinical research including EHR-embedded, remote no-touch, and platform trials, aligning with study needs;
2) Expand and enrich clinical trial capability by increasing potential participating site expression of interest (EOI) reach and readiness support (HBCUs and rural practice-based research networks), better process integration with CTSAs, preparing study teams, and broader expert engagement;
3) Innovate clinical trial methodology by creating, evaluating, and disseminating new methods for risk monitoring, AE reporting, direct EHR to REDCap data capture, and data standards to all CTSAs; and
4) Provide a distributed alliance of clinical and data coordinating centers with extensive and diverse expertise to offer support tailored for trial design, population, and condition.
Funding Goals
NOT APPLICABLE
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Nashville,
Tennessee
372031774
United States
Geographic Scope
Single Zip Code
Analysis Notes
Amendment Since initial award the total obligations have increased 191% from $5,169,803 to $15,054,272.
Vanderbilt University Medical Center was awarded
ECSTATIC: Engaging Cooperative Sites Trial Acceleration Trust Innovation Capability
Cooperative Agreement U24TR004437
worth $15,054,272
from National Center for Advancing Translational Sciences in June 2023 with work to be completed primarily in Nashville Tennessee United States.
The grant
has a duration of 4 years 10 months and
was awarded through assistance program 93.350 National Center for Advancing Translational Sciences.
The Cooperative Agreement was awarded through grant opportunity Limited Competition: Clinical and Translational Science Awards (CTSA) Consortium-Wide Centers: Resources for Rapid Demonstration and Dissemination (U24 Clinical Trials Optional).
Status
(Ongoing)
Last Modified 9/24/25
Period of Performance
6/29/23
Start Date
4/30/28
End Date
Funding Split
$15.1M
Federal Obligation
$0.0
Non-Federal Obligation
$15.1M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for U24TR004437
Transaction History
Modifications to U24TR004437
Additional Detail
Award ID FAIN
U24TR004437
SAI Number
U24TR004437-1330065165
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Nonprofit With 501(c)(3) IRS Status (Other Than An Institution Of Higher Education)
Awarding Office
75NR00 NIH National Center for Advancing Translational Sciences
Funding Office
75NR00 NIH National Center for Advancing Translational Sciences
Awardee UEI
GYLUH9UXHDX5
Awardee CAGE
7HUA5
Performance District
TN-05
Senators
Marsha Blackburn
Bill Hagerty
Bill Hagerty
Budget Funding
| Federal Account | Budget Subfunction | Object Class | Total | Percentage |
|---|---|---|---|---|
| National Center for Advancing Translational Sciences, National Institutes of Health, Health and Human Services (075-0875) | Health research and training | Grants, subsidies, and contributions (41.0) | $5,169,803 | 100% |
Modified: 9/24/25