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Patient Recruitment and Retention

    Clinical Trial Writing and DesignPatient EngagementPatient Recruitment and RetentionSite Materials & Logistics

    White Space is Not a Missed Opportunity in Clinical Study Materials

    by William McEwen March 3, 2026
    written by William McEwen

    Discover how print and digital clinical study materials, developed with clarity, white space, and purpose, improve participant understanding and engagement. White space refers to the empty area around print and design text and graphic elements.

    Long ago, in a different industry, I was part of a company’s creative team that wrote and designed ads that ran in the monthly trade magazines. When it came time for leadership to approve the latest ad, I knew one of the VPs would be resistant.

    Invariably, he would run his index finger across the white space in the ad and ask, “Are we missing an opportunity here?” In other words, we’re paying for a page, so let’s fill it with text.

    I was not unsympathetic. Budgets are real, and advertising isn’t cheap. Why tell potential customers about A, B, and C when there’s room to add D, E, and F? Fortunately, the company president understood the beauty and appeal of the design and knew it would stand out among the noise in all the pages around it. Predictably, he overruled the VP.

    Strategic Tool for Clinical Study Materials

    The idea I want to pass along here is this: Breathing room promotes breathing. And in patient materials, breathing room promotes comprehension, confidence, and action. White space is a vital strategic tool for enhancing readability, creating visual balance, minimizing user overwhelm, and directing focus.

    Every patient or participant material has one job: to be understood. When it takes on more, comprehension drops, and the piece loses the inviting quality that makes someone want to pick it up.

    At Imperial, we create numerous digital and print clinical study materials for participants across the globe, and the trifold brochure remains a reliable staple. It remains a classic tool because it’s familiar, portable, and easy to navigate.

    When a Document Loses Its Way

    It’s human nature to see every piece’s potential to do more, and the trifold brochure is a perfect example. During the writing process, we sometimes watch the word count swell into a four‑panel brochure and sometimes even a booklet. The writing process transformed it from a clinical study introduction into a mini ICF.

    When that happens, the material stops being a recruitment tool and becomes cumbersome, with too much detail to garner interest. If you’re inviting a potential participant to a study, your pieces should be inviting and easy to read.

    Key constraints to keep in mind:

    • Clean design requires 30-40 percent of the space for art and white space, which keeps the material readable and inviting.
    • Translation expansion adds 20-40 percent. If the English version barely fits, the translated version won’t fit at all.
    • Readers need natural stopping points. When every inch is filled, people lose their place and disengage.

    Keeping the main purpose of each material in mind can help prevent overstuffing it with unnecessary content.

    Final Thoughts

    The most effective materials are the ones people will actually use, not the ones that say the most. No matter the medium, from brochures to websites to videos, focused word count and intentional design make a piece more inviting and easier for the audience to engage with.

    The Imperial Advantage

    At Imperial, we start by defining the single job each material must do, and we design around that purpose while respecting the participant’s experience. Our teams understand how literacy, design, translation, and real-world use intersect. It’s how we turn digital and print clinical study materials into tools that work.

     

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  • Ancillary Trial Supplies and EquipmentBusiness InsightsClinical Trial Writing and DesignPatient EngagementPatient Recruitment and RetentionSite Materials & Logistics

    Discover Actionable Clinical Study Strategies: 7 Must-Read 2025 Blogs

    by William McEwen December 16, 2025
    by William McEwen December 16, 2025

    The Imperial blog team reviewed our 2025 blog posts and selected seven standout articles that offer valuable clinical study strategies to strengthen and streamline your clinical trials. Check them out! Clinical Trial Diversity Action Plans: 6 Key Components for Compliance Diversity action plans are now…

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  • Patient EngagementPatient Recruitment and RetentionTranslation of Study Materials

    The Power of Video in Clinical Trials: A Strategic Asset for Sponsors and CROs

    by Vaughn X. Anthony November 18, 2025
    by Vaughn X. Anthony November 18, 2025

    At the heart of every clinical trial are the people who choose to participate. They need reassurance, confidence, and trust in the process and in the research staff guiding them. Using video in clinical trials has the unique ability to meet those needs while also…

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  • Clinical Trial Writing and DesignLife-Science EventsPatient EngagementPatient Recruitment and Retention

    Maximizing Impact: Making the Most of Clinical Trial Communication

    by Mike Lakey November 4, 2025
    by Mike Lakey November 4, 2025

    This year has been packed with conferences, and we’ve recently closed out the latest: SCOPE Europe in Barcelona. The breakout agenda at SCOPE was strong, with timely topics and presenters who reminded us that great content is most effective when it’s paired with thoughtful delivery. The…

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  • Life-Science EventsPatient EngagementPatient Recruitment and Retention

    Patient Centricity in Clinical Trials: More Than a Talking Point

    by Imogen Cheese October 23, 2025
    by Imogen Cheese October 23, 2025

    Patient centricity in clinical trials has been a guiding theme across clinical research conferences for years, and lately, it’s begun to feel more real. At the recent SCOPE conference in Barcelona, I saw firsthand how sponsors are moving from intention to implementation. They are redesigning…

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  • Clinical Trial Writing and DesignPatient EngagementPatient Recruitment and RetentionSite Materials & Logistics

    Harnessing the Power of Print and Digital Clinical Trial Materials

    by Imogen Cheese September 9, 2025
    by Imogen Cheese September 9, 2025

    As clinical trials become increasingly complex and personalized, we need to take a fresh look at how we engage with patients—and with the wider community. That engagement often begins offline: a poster in a physician’s office, a leaflet picked up (for themselves or a loved…

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  • Clinical Trial Writing and DesignPatient EngagementPatient Recruitment and Retention

    Creating a Clinical Trial Website: What Are the 5 Essential Benefits and First Steps?

    by Mike Lakey July 9, 2025
    by Mike Lakey July 9, 2025

    “Google It.” Those two words encapsulate our modern approach to seeking information. And when it comes to research, the first instinct a potential participant may have is to jump online to find more details. But what happens if a suitable study lacks an online presence?…

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  • Business InsightsClinical Trial Writing and DesignPatient EngagementPatient Recruitment and Retention

    Clinical Trial Diversity Action Plans: 6 Key Components for Compliance

    by Vaughn X. Anthony May 14, 2025
    by Vaughn X. Anthony May 14, 2025

    Diversity in clinical trials is now mandated by law. While the importance of study diversity has long been emphasized, this marks the first time it has been codified into law under the Food and Drug Omnibus Reform Act of 2022 (FDORA).1 Through diversity action plans,…

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  • Business InsightsClinical Trial Writing and DesignPatient Recruitment and Retention

    The Upcoming FDA Clinical Trial Diversity Mandate: What You Need to Know

    by Vaughn X. Anthony May 14, 2025
    by Vaughn X. Anthony May 14, 2025

    In January 2024, I wrote about the FDA’s then-pending clinical research diversity requirements. Since that time, the regulatory landscape has shifted dramatically. This update outlines the most recent developments—including federal mandates under the Food and Drug Omnibus Reform Act (FDORA), the status of the FDA…

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  • Clinical Trial Writing and DesignPatient Recruitment and Retention

    How Do You Engage Pediatric Participants When Developing Clinical Trial Materials?

    by William McEwen March 25, 2025
    by William McEwen March 25, 2025

    Creating materials for pediatric participants, whether in digital or printed formats, presents unique challenges. This is due to the need to communicate complex ideas in simpler terms as well as create documents that appeal to that audience. Read on for tips to engage pediatric participants…

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Imperial Clinical Research Services Blog

Imperial is a global leader in clinical trial solutions and support, specializing in study and site print materials, ancillary trial supplies and equipment, clinical trial translation management, and clinical trial patient engagement.

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