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    Clinical Trial Materials Development and PrintingParticipant Engagement

    Digital Advertising in Clinical Trials: The Real Secret Sauce

    by Mike Lakey January 21, 2025
    written by Mike Lakey

    I’ve spent my entire adult life immersed in media, marketing, and advertising, long enough to remember the days before digital advertising in clinical trials took over. For patient recruitment, sponsors and CROs had little more to rely on than local newspapers and radio stations.

    They would earmark a modest budget, typically $2,000 to $3,000, and sites would collaborate with local media advertising representatives to place ads. Targeting meant placing an ad in the sports section for male participants or, to cast a wider net, running an ad on a country music station.

    Newspapers and radio stations were (and still are) a practical way to reach many people, but today, more options exist.

    Enter Digital Advertising: The Game Changer

    Digital advertising revolutionized patient recruitment. Here’s why it’s such a great tool for digital advertising in clinical trials:

    • Precision Targeting: Ads can reach select ages, genders, locations, and even specific health conditions—the exact people sponsors and CROs want to engage. Digital platforms are especially effective for zeroing in on distinct demographics.
    • Cost Efficiency: Pay-per-click models mean advertisers pay only when someone responds. Plus, campaigns can be tweaked on the fly without breaking the bank.
    • Speed and Scalability: Need to launch a campaign quickly? No problem. Need to expand the reach? This can be done easily.
    • User-Friendly Platforms: Step-by-step tools simplify setting up campaigns on popular platforms like Google and Facebook.

    Best Practices for Digital Advertising in Clinical Trials

    Yes, advertising has changed a lot over the years, but some of today’s best practices are timeless and predate the digital age:

    Best Practices for Digital Advertising in Clinical Trials

    1. Create Compelling Content
      Speak directly to potential participants with empathy and clarity.
    2. Use Visuals and Video
      Bright, engaging visuals and compelling videos grab attention and help explain complex ideas.
    3. Optimize Landing Pages
      A clear call to action is crucial. Make that step simple, like clicking on a clearly visible button to fill out a short pre-screener containing basic inclusion criteria.
    4. Leverage Analytics
      Regularly review click-through rates, conversions, and performance metrics. Test and tweak until you find what works.
    5. Adhere to Regulations
      Work closely with your legal and regulatory teams to stay compliant. This includes platform-specific rules, which can sometimes feel like solving a Rubik’s Cube blindfolded.

    But There’s a Twist

    All the fancy targeting, visuals, and optimizations won’t mean a thing without one crucial ingredient… follow-up.

    That’s right. Follow-up is crucial… you could call it the secret sauce.

    Imagine this scenario: You see an ad for a clinical trial. It sparks your interest, so you click through and complete a pre-screening questionnaire. Afterward, you’re informed that you qualify, and someone will contact you soon. How long should that take? Ideally, less than 24 hours. Realistically, no more than 48. But in actual practice? The average time for sites to follow up with referrals is often much longer.

    On a major phase 3 trial, our team worked to support dozens of sites with a robust digital advertising budget. Everyone was committed to enrollment. However, we found it took sites an average of six days to respond to potential participants who expressed interest in joining the study. That’s just too long. By this time, too many potential participants had moved on—mentally, emotionally, or both. Site teams are busy, there’s no denying that. It’s important to look for ways to reallocate resources to ensure a timelier response.

    Digital advertising in clinical trials is a powerful tool, but it’s just the start. To truly succeed, participants must know they are appreciated, and first impressions are lasting.

    A prompt follow-up isn’t just good manners; it’s essential to enrollment success. Because at the end of the day, digital ads might get someone to click, but it’s the personal connection that helps inspire them to commit.

    The Imperial Advantage

    Everything I’ve described are resources we can create for your trial. Traditional print tools like recruitment brochures, mini protocols, and physician letters are proven ways to connect with patients, sites, and medical professionals. Digital marketing expands the reach significantly and cannot be ignored. Contact us now to talk about how we can help with your study.

    January 21, 2025 1 comment
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  • Ancillary Clinical Trial Supplies and EquipmentClinical Trial Business InsightsClinical Trial Materials Development and Printing

    6 Clinical Study Blogs Not to Miss

    by William McEwen December 18, 2024
    by William McEwen December 18, 2024

    Our blog team reviewed our 2024 clinical study blogs, and we selected these six worth re-reading. Check them out! 1. Sustainability in Business: Transparency and Keeping Score ESG: Environmental, social, and governance are factors that influence commercial success. Discover how Imperial achieved a sustainability rating …

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  • Clinical Trial Business InsightsClinical Trial Materials Development and Printing

    International Clinical Trial Printing: Think Globally and Print Regionally

    by Ted Corrigan October 8, 2024
    by Ted Corrigan October 8, 2024

    Get highlights on how the international clinical trial printing vendor you select can impact everything from timelines to sustainability. Imperial supports numerous studies by writing, translating, designing, and printing clinical trial materials for sponsors, CROs, clinical research sites, and research patients. For this blog post, …

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  • Clinical Trial Materials Development and PrintingParticipant Engagement

    Tips for a Patient-Friendly Clinical Trial Informed Consent Form

    by William McEwen September 25, 2024
    by William McEwen September 25, 2024

    A patient-friendly informed consent form (ICF) is a key element for prospective clinical trial participants’ understanding of a clinical research study. In this blog, we delve into tips to ensure the ICF is clear and understandable. The research ICF document provides potential participants with the …

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  • Clinical Trial Materials Development and PrintingParticipant Engagement

    Long-Term Clinical Trial Participation: 6 Tips to Retain and Keep Patients Engaged

    by Kori Ammon September 12, 2024
    by Kori Ammon September 12, 2024

    Retaining participants in studies is an ongoing challenge that the clinical trials industry grapples with daily. One analysis1  I came across pegged the participant dropout rate at an average of 25-26 percent per study. Every single loss is costly and, among other problems, can prolong …

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  • Clinical Trial Business Insights

    Mastering Clinical Trial Timelines

    by Heather Ross August 20, 2024
    by Heather Ross August 20, 2024

    Realistic, well-managed clinical trial timelines are essential to the success and timeliness of clinical studies. Read on for more information about keeping your projects on track. We often say every clinical trial is made up of a million moving parts. The materials, equipment, and supplies …

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  • Clinical Trial Materials Development and PrintingParticipant Engagement

    Writing Clinical Study Materials: Connect with Patients and Professionals

    by William McEwen August 6, 2024
    by William McEwen August 6, 2024

    Whether you’re a sponsor, CRO, or part of a study team, writing clinical study materials that resonate with your audience is crucial for recruitment, referrals, and retention. Our tips will get you started and guide you through the writing process. You know all the standard …

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  • Clinical Trial Materials Development and PrintingParticipant EngagementTranslation of Clinical Trial Materials

    Clinical Research Translation: Can You Manage all the Moving Parts?

    by Heather Ross May 2, 2024
    by Heather Ross May 2, 2024

    Clinical research translation affects almost every global study. Understanding the translation process and the planning required can help keep your study on track. Clinical trial statistics can be surprising. We frequently write about different aspects of the growing complexity of global clinical trials. Despite the …

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  • Clinical Trial Business Insights

    3 Tips to Make Your Clinical Trial Teams Agile and Proactive

    by Ted Corrigan March 6, 2024
    by Ted Corrigan March 6, 2024

    Clinical trial teams must be agile and proactive in the evolving world of clinical studies. Research teams navigating today’s dynamic landscape face a multitude of risks due to the ever-increasing pace of change. These risks can include: Technological advances rapidly rendering initial plans obsolete Supply …

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  • Ancillary Clinical Trial Supplies and EquipmentClinical Trial Materials Development and PrintingParticipant Engagement

    6 Top Picks: Clinical Trial Blogs Not to Miss

    by William McEwen December 27, 2023
    by William McEwen December 27, 2023

    The Imperial blog team took a look at our 2023 clinical trial blogs, and we’re shining the spotlight on our top six picks. So here they are, in no particular order: six clinical trial blogs worth reading (and re-reading). 1. Supply Chain: Master these key …

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