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Under Pressure: Designing Patient Centric Trials That Beat Complexity, Earn Trust, and Improve Retention
Facing the New Reality: Clinical Trials Under Pressure
Sue Harris, Director Content Development
Jan 05, 2026

The landscape of clinical trials is undergoing seismic change, driven by mounting pressures that sponsors and sites can no longer afford to ignore. Rising protocol complexity, fierce competition for patient enrolment, and the demand for real-world evidence are colliding with persistent barriers—such as patient mistrust, digital divides, and regulatory scrutiny. Today, the challenge isn’t just to run compliant studies, but to design trials that genuinely address the needs and expectations of diverse patient populations. The stakes are higher than ever: delays, dropouts, and disengagement can jeopardize not only timelines and budgets, but also the scientific and ethical integrity of research.

The Urgency of Patient-Centric Transformation

In this climate, patient-centricity is no longer a buzzword—it’s a strategic imperative. Sponsors and sites must move beyond traditional models and confront the realities patients face: logistical burdens, lack of transparency, and limited support throughout the trial journey. When trials are designed with empathy and flexibility, patients are empowered to participate fully, leading to faster recruitment, improved retention, and richer data. More importantly, it means clinical research can deliver outcomes that matter—not just to regulators and sponsors, but to the people whose lives depend on innovation.


Building a Patient-Centric Strategy

So, how can sponsors and sites put patients at the center of their trials? It starts with understanding what matters most to participants. Surveys, interviews, and social listening can reveal valuable insights about patient preferences and pain points. With this information, teams can customize support resources—like study nurses, travel assistants, and registered dieticians—to reduce barriers and make participation more comfortable.

Technology also plays a key role. Engagement platforms and connected devices help streamline communication, making it easier for patients to stay informed and for sites to manage data collection.


Recruitment and Retention: What Works

Recruitment doesn’t have to be a bottleneck. Multi-channel outreach—combining digital campaigns with traditional methods—can reach a wider range of patients. Direct-to-patient campaigns target individuals based on location, demographics, and clinical criteria, while site enablement ensures coordinators and research assistants are available to help manage recruitment efficiently.

Retention is just as important. Decentralized trial components, such as televisits and remote support, reduce travel and time burdens. Personalized communications, including reminders and motivational messages, keep patients engaged and motivated to complete the study.


Listening to the Patient Voice

Engaging content starts with empathy. Developing patient personas and mapping out the trial journey helps sponsors and sites identify where participants might need extra support. Behavioral science can guide messaging that addresses emotional and psychological needs, not just clinical information. Testing materials with patients and advocacy groups ensures that communications are clear, accessible, and relevant.


Branding and Visual Identity

Trust is built through consistency. Professional, recognizable branding across all study materials helps patients feel confident in the trial. Inclusive design—tested with patient communities—ensures visuals and messaging resonate with diverse populations. Tailoring branding to specific therapy areas further strengthens engagement.


Making Trials Accessible and Inclusive

Accessibility means more than just translating materials. Providing information in print, digital, and multimedia formats ensures patients can access content in ways that suit them best. Adapting language and cultural references makes materials more relatable, while continuous feedback from patients and sites helps teams refine their approach.


Technology-Driven Engagement

Digital tools are transforming the patient experience. Patient engagement apps offer flexible scheduling, virtual visits, and secure messaging. Gamification—using interactive modules and rewards—can motivate compliance and retention. Ensuring all digital solutions meet privacy and security standards is essential for building trust.


Holistic Patient Support

One innovation making a real difference is remote access to registered dieticians. Available in dozens of countries, this service supports patients not only in obesity trials, but also in oncology, cardiovascular, and hepatology studies. By aligning diet and lifestyle support with study protocols, sponsors and sites can offer personalized guidance that improves the overall trial experience.


Conclusion: Delivering Trials Patients Want to Join

Pharma sponsors and sites have a unique opportunity to transform clinical trials by putting patient experience at the heart of every decision. By adopting patient-centric strategies, leveraging technology, and fostering continuous improvement, you can accelerate recruitment, boost retention, and deliver studies that truly make a difference.

If you’re ready to enhance your trial outcomes and create a more impactful experience for patients, reach out to IQVIA’s Patient and Site Centric Solutions team. Together, we can design trials that patients want to join—and stay engaged in.

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