August 8, 2024: FDA Commissioner and NIH Director Share Thoughts on the Future of Pragmatic Clinical Trials

Speaking at the NIH Pragmatic Trials Collaboratory’s 2024 Annual Steering Committee Meeting in May, Commissioner of Food and Drugs Robert Califf and NIH Director Monica Bertagnolli discussed the intersection of pragmatic research and national health priorities.

Califf and Bertagnolli spoke about the role the NIH Collaboratory can play in promoting scientifically rigorous, pragmatic clinical research that addresses the urgent need for better and faster implementation of research findings into patient care. They also addressed shortcomings of the electronic health record (EHR) and the challenges of building a learning health system.

Dr. Monica Bertagnolli and Dr. Robert Califf speak at the NIH Pragmatic Trials Collaboratory's 2024 Annual Steering Committee Meeting

Wendy Weber of the National Center for Complementary and Integrative Health moderated the discussion, which focused on 3 challenges in clinical research and their relation to the NIH Collaboratory:

  • Medical providers and patients lack scientific evidence to support medical decisions
  • A learning health system can help to develop this evidence, but challenges in developing this system remain
  • How can the NIH Pragmatic Trials Collaboratory aid in these challenges?

“The most fundamental flaw we have in general right now is that we don't tell people that their biggest risk is getting standard healthcare in the healthcare system,” Califf said.  “Without evidence, clinicians don't actually know what to do. We act like we know, but we don’t,” he added.

Medical providers and patients alike must often make underinformed decisions. The lack of scientific evidence to support these decisions poses a challenge, as it demands clinicians use their individual experience and judgment when making a recommendation. Here, the deficiencies of the EHR become most obvious, as it fails to meet the needs of the population by not providing sufficient data for providers to refer to. Bertagnolli emphasized this, stating the EHR needed to become a learning environment, facilitating both the collection and dissemination of knowledge even for busy doctors.

“We need to reach every person,” Bertagnolli challenged the researchers in the audience. “We need to get in every corner of the United States with our data, with our research. We need to make it possible for busy doctors and clinics to be in a learning environment,” she said.

“What's the one unifying bit of technology we have that is not delivering what we need? It's the electronic health record,” Bertagnolli added.

Developing a health system that fosters collaboration and constant learning is paramount to obtaining generalizable medical evidence. Califf emphasized this need, calling for a singular “voice” that can represent the population’s prevention and health issues, collectively demonstrating what works.

However, several barriers hinder the development of such a system. The healthcare industry often finds that delivery practices that optimize profit margins are not optimal for patient health outcomes, which creates an environment of ethical uncertainty. Furthermore, the United States spends more on healthcare than do comparable countries with higher life expectancies, leading to unnecessary expenditures and unwillingness to adopt new initiatives.

“We're paying for a lot of things that don't help. So how are we going to figure out what to stop doing?” Bertanolli asked. “The only way is data. And the only people who can bring that data are our care providers to collect those data and learn from them. It is imperative to get a learning health system in progress,” she said.

The NIH Pragmatic Trials Collaboratory has long played a role in establishing cost-effective, large-scale research that treats care providers as research partners to deliver generalizable, actionable data. The program’s efforts in promoting collection of data from clinical care environments ensure that research remains grounded in real-world patient outcomes. Moreover, the NIH Collaboratory's emphasis on gathering data from underrepresented populations enhances the relevance of research findings, addressing disparities in healthcare delivery and outcomes.

Along with data collection, Bertagnolli encouraged the NIH Collaboratory to be an advocate for this new health system and encourage organizations to participate in the development of this system. The NIH Collaboratory brings years of specialized clinical knowledge and input, ensuring that the system is informed by evidence-based practices and responsive to the needs of both care providers and patients.

“It's a matter of convincing people to get over the hump, embrace a learning health system, and participate—and specifically, I'd say get the wheel turning as fast as you can, answer as many questions as you can, and talk about it,” added Califf.

View the full materials from the 2024 Annual Steering Committee Meeting.

August 6, 2024: Workshop Materials Now Available From NIH-Hosted Workshop, ‘Going From Zero to 100: Generating Evidence Through Pragmatic Research to Address Pressing Healthcare Issues’

Materials and videocast recordings are now available from the NIH Pragmatic Trials Collaboratory’s recent workshop, “Going From Zero to 100: Generating Evidence Through Pragmatic Research to Address Pressing Healthcare Issues. The 2-day workshop, hosted by the NIH, featured a keynote address by NIH Director Monica Bertagnolli exploring how to identify high-priority healthcare issues that require the effort, time, and funding of a clinical trial.

The first day of the workshop focused on “Phase Zero,” the preparatory phase of pragmatic research in which investigators explore how to align their research question with the priorities of patients, funders, and healthcare systems to address urgent issues and generate actionable evidence. The second day of the workshop explored challenges associated with launching a pragmatic trial, including ensuring an interoperable data set, enrolling a representative patient population, and securing contracts, data use agreements, and institutional review board approval.

Access the complete workshop materials, including slides and videocast recordings.

Session 1: Phase Zero: Getting the Research Question Right

Session 1 provided real-world examples of how investigators developed their research questions with the help of patients, funders, and healthcare system partners. This “Phase Zero” in pragmatic trials research includes framing the research question in the right way and selecting meaningful outcomes. Access the complete workshop materials and videocast recordings.

Panelists: Kevin McLaughlin, Kushang Patel, Andrea Cheville, Gregory Simon; Moderator: Kevin Weinfurt

Session 2: Engagement as the Cornerstone in Pragmatic Research

Session 2 explored engagement with research partners, including real-world examples of how and when researchers identified and approached frontline clinicians, patients, funders, and community partners. Panelists shared how best to convey information in a way that builds trustworthiness and a foundation for meaningful engagement over time. Access the complete workshop materials and videocast recordings.

Panelists: Natalia Morone, Julie Fritz, Anna Krupp, Sebastian Tong; Moderator: Gregory Simon

Session 3: How to Use Data From Disparate Data Systems

Session 3 focused on making sense of disparate data systems early in the research process and ensuring that an interoperable data set is ready for analysis at the end of the trial. Panelists discussed pros and cons of adhering to a common data model, ways of simplifying data collection and data sharing, and collecting complementary and integrative health information. Access the complete workshop materials and videocast recordings.

Panelists: Elizabeth Wick, Chandra Almond, Leslie Crofford; Moderator: Keith Marsolo

Session 4: Retrofitting, Reimagining, and Redesigning Health Care Systems to Reach Populations Most Affected by Health Inequities

Session 4 focused on approaches to ensuring that populations most affected by health inequities in the condition being studied are included in research. Panelists discussed how to ensure that healthcare systems in both resource-rich and underserved settings are research-ready to engage historically marginalized populations. Access the complete workshop materials and videocast recordings.

Panelists: Diana Burgess, Eduard Vasilevskis, Gloria Coronado; Moderator: Rosa Gonzalez-Guarda

Session 5: Overcoming Administrative Burden in Pragmatic Research

Session 5 explored ways to overcome administrative burdens in pragmatic research, including burdens associated with contracts, data use agreements, and institutional review board review and approval. Panelists with experience conducting NIH Collaboratory Trials shared lessons, successes, and failures. Access the complete workshop materials and videocast recordings.

Panelists: Karen Hartman, Geeta Swamy, Pearl O’Rourke, Keith Marsolo, Michael Kurilla, Michael Ho, Miguel Vazquez; Moderator: Adrian Hernandez