Unlocking the power of primary care in chronic disease research

Build a more scalable, representative and patient-centered approach to chronic disease trials by bringing research closer to where patients receive care.

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Traditional clinical trial recruitment and site engagement models are under growing strain. As chronic disease studies become more competitive and complex, sponsors are often relying on the same established research sites, patient populations and geographies, while many eligible patients remain outside the reach of clinical research.

This white paper explores how integrating primary care and community-based practices into chronic disease research can expand patient access, improve representation and create more flexible pathways for participation.

Inside, you’ll learn how to:

Understand why traditional recruitment and site engagement models are reaching their limits in chronic disease research

Explore how primary care can support broader patient access, stronger trust and more representative enrollment

Identify common barriers that prevent primary care practices from participating in clinical research

Apply flexible participation models that allow primary care providers to engage as referral partners, sub-investigators or fully enabled research sites

Build a more patient- and provider-centered ecosystem through operational support, digital solutions and decentralized trial delivery

Download the white paper to learn how sponsors can bring chronic disease research closer to routine care and build more scalable and inclusive trial delivery models.

Expand access, representation and recruitment in your chronic disease clinical trials.

Complete the form below to download the white paper.