STUDY DESIGN

With ACT, researchers can explore patient populations in depth and in real time. At the design stage, use ACT to learn about your patient population and iteratively test and refine clinical study parameters.

COHORT DISCOVERY FEASIBILITY

With ACT, researchers can iteratively test and refine inclusion and exclusion criteria. Use ACT to confirm the feasibility of your clinical study.

COLLABORATION

With ACT, researchers can search patient populations across the CTSA network in a HIPAA-compliant manner from their desktop. Use ACT to identify partners for multi-site studies.

FUNDING

With ACT, researchers can access easy-to-download results for use in funding proposals. Use ACT to demonstrate the feasibility of your clinical study to potential funders.

ETHICS / COMPLIANCE

With ACT, researchers can access easy-to-download results for use in IRB submissions. Use ACT to demonstrate recruitment feasibility for your study to IRB.

RECRUITMENT

Under development: ACT will introduce technology to facilitate re-identification of patients for clinical study recruitment, in accordance with each participating institution’s existing IRB protocols.