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NIH Collaboratory
Living Textbook of
Pragmatic Clinical Trials

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Rethinking Clinical Trials

A Living Textbook of Pragmatic Clinical Trials

  • Design
    • What is a Pragmatic Clinical Trial?
    • Decentralized Pragmatic Clinical Trials
    • Developing a Compelling Grant Application
    • Experimental Designs and Randomization Schemes
    • Endpoints and Outcomes
    • Analysis Plan
    • Using Electronic Health Record Data
    • Building Partnerships and Teams to Ensure a Successful Trial
    • Intervention Delivery and Complexity
    • Patient Engagement
  • Data, Tools & Conduct
    • Assessing Feasibility
    • Acquiring Real-World Data
    • Assessing Fitness-for-Use of Real-World Data
    • Study Startup
    • Participant Recruitment
    • Monitoring Intervention Fidelity and Adaptations
    • Patient-Reported Outcomes
    • Clinical Decision Support
    • Mobile Health
    • Electronic Health Records–Based Phenotyping
    • Navigating the Unknown
  • Dissemination & Implementation
    • Data Sharing and Embedded Research
    • Dissemination Approaches for Different Audiences
    • Implementation
    • End-of-Trial Decision-Making
  • Ethics & Regulatory
    • Privacy Considerations
    • Identifying Those Engaged in Research
    • Collateral Findings
    • Consent, Disclosure, and Non-Disclosure
    • Data and Safety Monitoring
    • Ethical Considerations of Data Sharing in Pragmatic Clinical Trials
    • Ethics for AI and ML
    • IRB Responsibilities and Procedures

Establishing Close Partnerships With Participating Healthcare System Leaders and Staff

CHAPTER SECTIONS

Assessing Feasibility


Section 3


Establishing Close Partnerships With Participating Healthcare System Leaders and Staff

Expand Contributors

Lynn L. DeBar, PhD, MPH
Jeffrey G. Jarvik, MD, MPH
Leah Tuzzio, MPH
Miguel A. Vazquez, MD

Contributing Editors
Liz Wing, MA
Karen Staman, MS

Conducting PCTs embedded in healthcare system settings requires efforts at directly involving diverse interest holders, including delivery system leaders, operational personnel, IT staff, statisticians, frontline care providers and patients. Input from these interest holders is an important part of the trial’s design and planning. Establishing and maintaining good relationships and communication are essential for the long-term success of the trial.

Study teams should identify at least one co-investigator at each study site who will serve as an integral project member and a site champion over the course of the project. Having such a research partner is important in understanding who is affected by the embedded elements of your intervention. Champions not only can identify inefficiencies or constraints not evident at higher levels of the organization, but also have experience in fixing problems internally. Choosing the right partner is critical. They need to have enough experience to know how to effectively troubleshoot within their system and have the respect of system leaders and influence within their organization to implement solutions. Both the study team and the healthcare system may need to make adjustments or accommodations for competing priorities throughout the trial planning and execution phases.

The following table gives example scenarios of building partnerships from the NIH Collaboratory Trials.

Establishing Partnerships Examples
Scenario Research Team Approach
EHR programming staff at the site prioritized clinical needs over research needs, which led to delays in data pulls for the trial. Engaged with site programmers early in the project to help them develop and maintain an investment in the trial’s purpose and research methods. A helpful approach is to have the study team regularly informed of the programmers’ priorities. Clinical-based programmers generally have different priorities than research-based programmers.
Intervention was in the primary care setting where schedules are busy and space is tight. Teamed with clinicians to understand workflow and schedule study-related patient visits during slower clinic periods and held patient visits in less conventional ways (after hours, groups met in lobby spaces).
There were high amounts of leadership turnover at medical director and provider levels due to preexisting pressures and challenges inherent in community clinics. Met regularly with leadership teams and established an advisory board and other infrastructure to help engage leaders and gatekeepers.
Leadership approval of the study was delayed because different departments within a single healthcare system were unable to initiate approval without the other departments going first. For example, Interest holder A could not approve the study before Interest holder B approved. Facilitated in-depth discussions of the project with all the relevant interest holders on the phone or web at the same time, when face-to-face meetings were not possible. A prior history of collaboration among investigators and support from senior officers in the healthcare systems was instrumental in obtaining approval.
Gaining widespread support from health system interest holders was essential before implementing the intervention. Leveraged the health systems’ previous experience in conducting embedded clinical research. Health system and clinic leaders were enthusiastic about how the intervention, if successful, could fill a service gap.

 

Previous Section Next Section

SECTIONS

CHAPTER SECTIONS

sections

  1. Introduction
  2. Developing the Trial Documentation
  3. Establishing Close Partnerships With Participating Healthcare System Leaders and Staff
  4. Delineating the Roles of All Interest Holders to Determine Training Needs
  5. Pilot Testing
  6. Feasibility Assessment Scenarios From the NIH Collaboratory Trials
  7. Spotlight on NIH Collaboratory Trials
  8. Additional Resources

Resources

Learn more in the chapter Building Partnerships to Ensure a Successful Trial

These articles by members of the NIH Collaboratory’s Health Care Systems Interactions Core contain tips and guidance for pragmatic trial study teams:

  • A guide to research partnerships for pragmatic clinical trials (Johnson KE, et al. BMJ 2014).
  • Trials without tribulations: minimizing the burden of pragmatic research on healthcare systems (Larson EB, et al. Healthcare 2015).


Version History

August 27, 2020: Added a new scenario to the table and made nonsubstantive changes to text as part of annual content update (changes made by L. Wing).

December 10, 2018: Added a new scenario to the table (changes made by L. Wing).

Published August 25, 2017

current section :

Establishing Close Partnerships With Participating Healthcare System Leaders and Staff

  1. Introduction
  2. Developing the Trial Documentation
  3. Establishing Close Partnerships With Participating Healthcare System Leaders and Staff
  4. Delineating the Roles of All Interest Holders to Determine Training Needs
  5. Pilot Testing
  6. Feasibility Assessment Scenarios From the NIH Collaboratory Trials
  7. Spotlight on NIH Collaboratory Trials
  8. Additional Resources

Citation:

DeBar LL, Jarvik JG, Tuzzio L, Vazquez MA. Assessing Feasibility: Establishing Close Partnerships With Participating Healthcare System Leaders and Staff. In: Rethinking Clinical Trials: A Living Textbook of Pragmatic Clinical Trials. Bethesda, MD: NIH Pragmatic Trials Collaboratory. Available at: https://rethinkingclinicaltrials.org/chapters/conduct/assessing-feasibility/establishing-close-partnerships-with-participating-healthcare-system-leaders-and-staff/. Updated July 2, 2024. DOI: 10.28929/055.

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