Disseminating, Implementing, and Sustaining Evidence-Based Practices Into Clinical Care: NIH-Hosted Workshop (May 2017)

May 24, 2017: This workshop identified best practices for the dissemination, implementation, and sustainability of ePCT findings. When conducted within integrated healthcare systems, ePCTs can leverage existing infrastructure to answer important clinical questions in a cost-effective manner.

Agenda and Slides

Welcome and Introduction

Josephine Briggs, MD
Richard Hodes, MD
Catherine Myers, MD
Wendy Weber, ND, PhD, MPH

Keynote: An Orientation to Dissemination, Implementation, Sustainability De-Implementation and the Science of Making Science Matter

David Chambers, DPhil

Panel 1: Setting the Stage for Dissemination and Implementation

Moderator: David Chambers, DPhil

Panel:

    • Susan Huang, MD, MPH
    • Doug Zatzick, MD
    • Gloria Coronado, PhD

Panel 2: Health System Engagement: Partnership, Relationships, and Transparency

Moderator: Eric Larson, MD, MPH

Panel:

    • Miguel Vazquez, MD
    • John Warner, MD
    • Lynn DeBar, PhD, MPH
    • Andrew Bertagnolli, PhD
    • Vincent Mor, PhD

Panel 3: Swimming with the Sharks - Translation of Pragmatic Trial Results

Moderator: Lesley Curtis, PhD
Presenter: Greg Simon, MD, MPH

Panel:

    • Susan Mullaney, MHA
    • Edward Septimus, MD
    • Matt Hough, MD

Panel 4: Designing for Sustainability

Moderator: Amy Kilbourne, PhD, MPH

Panel:

    • Laura Dember, MD
    • Jerry Jarvik, MD, MPH
    • Patrick Luetmer, MD
    • Greg Simon, MD, MPH

Panel 5: Stakeholder Reactions Panel Discussion

Moderator: Catherine Myers, MD

Panel:

    • John Warner, MD
    • Susan Mullaney, MHA
    • Amy Kilbourne, PhD, MPH

Summary and Concluding Remarks

Ethical and Regulatory Issues of Pragmatic Clinical Trials: NIH-Hosted Workshop (May 2016)

May 10, 2016: This workshop focused on unique ethical and regulatory issues identified by the NIH Collaboratory Trials supported by the NIH Health Care Systems Research Collaboratory Program.

Agenda and Slides

Welcome and Introduction

Catherine Myers, MD
Wendy Weber, ND, PhD, MPH

Keynote: Addressing the Ethical and Regulatory Issues in Pragmatic Clinical Trials

Jeremy Sugarman, MD, MPH

Panel 1: Options for Altered Consent and the Importance of Minimal Risk Determination

Moderator: Kevin Weinfurt, PhD

Panel:

    • Laura Dember, MD
    • Gregory Simon, MD, MPH
    • John Lantos, MD
    • Emma Meagher, MD

Panel 2: Oversight of Pragmatic Clinical Trials: Institutional Review Boards and Data and Safety Monitoring Boards

Moderator: Adrian Hernandez, MD, MHS

Panel:

    • Douglas F. Zatzick, MD
    • P. Pearl O'Rourke, MD
    • Susan S. Ellenberg, PhD

Panel 3: Privacy Issues for Pragmatic Clinical Trials

Moderator: Valerie Bonham, JD

Panel:

    • Sarah M. Greene, MPH
    • Valery Gordon, PhD, MPH
    • Miguel Bazquez, MD

Panel 4: Vulnerable Populations

Moderator: David Wendler, PhD

Panel:

    • Susan S. Huang, MD
    • Mary Jane Welch, DNP, APRN, BC

Panel 5: Expert Panel Q&A

Moderator: Jeremy Sugarman, MD, MPH

    • Kevin Weinfurt, PhD
    • Adrian Hernandez, MD, MHS
    • Valerie Bonham, JD
    • David Wendler, PhD

Summary and Concluding Remarks