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Common Concerns About Clinical Trials—And What We Can Do About Them

Common Concerns About Clinical Trials—And What We Can Do About Them

Forbes21-07-2025
Sonali Bloom is CEO of 20/20 Onsite.
When people hear the term 'clinical trial,' they often imagine someone with a serious illness, desperate for a last-resort treatment, being poked and prodded in a lab. These images are persistent, but far from the truth. In my years of experience working with clinical trials, I've learned that while some of the concerns people have are valid, many are rooted in misunderstanding.
These misconceptions have a significant impact on how broad and effective our clinical research can be. When we can't recruit or retain the right participants, it slows the pace of medical advancement for everyone. But the good news is that we have real, actionable ways to address these issues, starting with education and a patient-first approach to clinical trial design.
Not Just For The Sick
One of the most common misconceptions I hear is that trials are only for people who are seriously ill. In reality, healthy volunteers play a critical role in clinical research. Drug developers need a baseline, like a statistical 'blank slate,' to see how new treatments affect the body without the complications of an existing condition.
This misconception often goes hand in hand with the belief that trials are only for those who have exhausted every other option. That narrative is just as inaccurate. Many trials are designed specifically for people at the beginning of their treatment journey. Clinical trials can offer alternatives that are less invasive or more promising, such as a pill for an ophthalmologic condition instead of injections or surgery. That alone can be a compelling reason to participate in a trial sooner, rather than later.
We can't talk about hesitations around clinical trials without addressing the issue of historical distrust. In some communities, especially those that have been mistreated or exploited by the medical establishment, this skepticism is deep-rooted and understandable. But today, clinical research is one of the most highly regulated parts of healthcare. Participant safety is paramount, and researchers are required to adhere to strict protocols and uphold stringent ethical standards. Nonetheless, trust is earned, not granted.
The impact of these concerns is not academic. They directly affect who participates in trials and who doesn't. Right now, trial participants tend to come from a narrow demographic, often concentrated in cities around research hubs. This lack of variety in age, background, and lived experience can lead to blind spots in treatment efficacy, safety, and applicability.
Building Trust And Breaking Barriers
Let's be honest: Participating in a clinical trial can be inconvenient. There may be travel involved, time away from work or family, and experimental medical procedures don't always work. But the reality is changing fast. We're seeing a wave of innovation in technology and trial design aimed at reducing patient burden.
Remote monitoring, mobile clinics and at-home test kits are making participation more convenient and accessible. Why drive to a hospital when a nurse can come to you, or you can test yourself at home and log your data on a smartphone? These kinds of features are essential if we want to recruit and retain a more diverse group of participants. And for many patients, financial compensation is an added incentive. In some cases, you're essentially receiving cutting-edge care, often years before it's widely available, for free.
Education is our strongest tool for getting the truth out. When people understand the purpose, value and reality of clinical research—not just for themselves, but for society—it helps normalize the process and reframes the conversation. Clinical trials are an integral part of the healthcare ecosystem. Helping people see that connection builds trust and encourages a wider swath of society to participate. The result: better outcomes on all sides.
Education also helps foster a sense of gratitude. When you understand the rigorous process a drug or procedure undergoes before it reaches your pharmacy or doctor's office, you're more likely to appreciate the people who helped test and develop it.
Even if the benefit of taking part in a clinical trial isn't immediate or personal, your participation could help a family member, a neighbor or someone else in your community down the line. When more people see trials in this light, we can help shift the conversation from 'Why me?' to 'Why not me?'
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