Differences

This shows you the differences between two versions of the page.

Link to this comparison view

Both sides previous revision Previous revision
Next revision Both sides next revision
projects [2018/05/14 22:24]
shyam [Accrual of patients to Clinical Trials (ACT) network] 		projects [2018/05/14 22:25]
shyam [Accrual of patients to Clinical Trials (ACT) network]
Line 24: Line 24:
  
 ==== Accrual of patients to Clinical Trials (ACT) network ==== ==== Accrual of patients to Clinical Trials (ACT) network ====
-{{ wiki:act.png?150x0}}+{{ wiki:act.png?200x0}}
  
 The [[https://www.act-network.org/|Accrual of patients to Clinical Trials (ACT) network]] is a nationwide network of sites that share EHR data to significantly increase participant accrual to the nation’s highest priority clinical trials. It is funded by NCATS' Clinical and Translational Science Awards (CTSA) program that supports efforts to solve system-wide translational research problems to improve the success of U.S. clinical trials. The ACT network is built on existing platforms (i2b2/SHRINE) to create a federated network with common standards, data terminology and shared resources. The ACT investigators are focused on 1) data harmonization across EHR platforms, 2) technical needs assessment and implementation, 3) regulatory approaches to ensure compliance with protocols for data access and participant contact, and 4) governance development to establish proper agreements among institutions. More information is available at [[https://ncats.nih.gov/pubs/features/ctsa-act|NCATS]]. The [[https://www.act-network.org/|Accrual of patients to Clinical Trials (ACT) network]] is a nationwide network of sites that share EHR data to significantly increase participant accrual to the nation’s highest priority clinical trials. It is funded by NCATS' Clinical and Translational Science Awards (CTSA) program that supports efforts to solve system-wide translational research problems to improve the success of U.S. clinical trials. The ACT network is built on existing platforms (i2b2/SHRINE) to create a federated network with common standards, data terminology and shared resources. The ACT investigators are focused on 1) data harmonization across EHR platforms, 2) technical needs assessment and implementation, 3) regulatory approaches to ensure compliance with protocols for data access and participant contact, and 4) governance development to establish proper agreements among institutions. More information is available at [[https://ncats.nih.gov/pubs/features/ctsa-act|NCATS]].