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CTSA Subcommittee (*= SC member)

CTSA Subcommittee (*= SC member). John Speakman , CBIIT, NCI Neesha Desai (Facilitator), CBIIT, NCI *Bob Annechiarico, Duke Comprehensive Cancer Center *Chris Chute, MD, PhD, MPH, Mayo Clinic, Minnesota Leslie Derr , CBIIT, NCI Brad Erickson, MD, PhD, Mayo Clinic, Minnesota

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CTSA Subcommittee (*= SC member)

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  1. CTSA Subcommittee (*= SC member) • John Speakman, CBIIT, NCI • Neesha Desai (Facilitator), CBIIT, NCI • *Bob Annechiarico, Duke Comprehensive Cancer Center • *Chris Chute, MD, PhD, MPH, Mayo Clinic, Minnesota • Leslie Derr, CBIIT, NCI • Brad Erickson, MD, PhD, Mayo Clinic, Minnesota • Ed Helton, CBIIT, NCI • *Warren Kibbe, PhD, Northwestern University • Paul Mulhern, CBIIT, NCI • *Sorena Nadaf, University of California San Francisco • *Ida Sim, PhD, University of California, San Francisco

  2. Clinical and Translational Science AwardsSubcommittee Update • Remit: Identify strategies and develop plans for Clinical and Translational Science Awards (CTSA)/caBIG® collaboration • REDCap and Case Report Form (CRF) collaboration • Loaded demography module into REDCap • Translated the demography CRFs into a general format to load into REDCap • Discussed utilization of REDCap as an interface to the caBIG® Clinical Trials Suite • REDCap to Metadata Services to build forms • CRF Template Management Service – stores your CRFs in a standard template (CDA based CRFs). REDCap can interact with this service to retrieve the CRFs. • REDCap can be used as an instance service • REDCap can integrate with the suite and leverage other enterprise services at NCI – can be used to collect various type of information • Scheduling component of REDCap to work with calendars, Adverse Events (AEs)

  3. CTSA Subcommittee Update • Next Steps • Further explore integration opportunities with the caBIG® Clinical Trials Suite • Continue loading additional CRF modules into REDCap

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