Patient Recruitment/Retention Featured Articles
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The Problem With Excluding Children From GLP-1 Trials In The U.S.
2/19/2026
In the U.S., roughly 15 million children are obese. But many are excluded from GLP-1 research. Obesity expert Evan Nadler, MD, explains why that's problematic.
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How AI-Enabled Personal Health Tools Are Reshaping Clinical Trial Workflows
2/17/2026
Learn how AI-enabled personal health technologies are impacting key aspects of trial operations while also exploring operational challenges that clinical operations leaders must manage in this AI-driven era.
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4 Steps For Representative Enrollment In Rare Disease Trials
2/16/2026
Discover the D.A.T.A. method and its utility in enrolling diverse representative patient populations in rare disease clinical trials.
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Heard At SCOPE: Pharma Wants ROI For Patient Data Return, Diverse Enrollment
2/11/2026
Twice I heard “ROI is the elephant in the room.” Two different panel discussions, two different tracks.
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The FDA Calls For Culturally-Informed Research, But What Do We Understand About The Sikh Community?
2/9/2026
Despite the size and visibility of the community — and the call for diverse patient research — there remains a gap in available health data specific to the Sikh community in the U.S.
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The Key Role Of Clinical Supply Teams In Patient Centricity Efforts
2/9/2026
Clinical supply decisions shape patient access, safety, and trial success. From logistics to procurement, patient-centric supply can accelerate therapies or quietly delay them.
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Building Patient Trust In Research Through Connection Driven-Transparency
2/4/2026
The question is not whether trust matters but how industry, sponsors, and investigators can bridge the trust gap to drive patient participation.
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Patient Trust In Pharma Is Low; Here's How To Rebuild It
2/2/2026
CISCRP's Annick de Bruin and Shalome Sine provide strategies for building patient trust based on the findings from their Perceptions & Insights Study.
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How Gilead Includes Patients Most Affected By HIV In Its PrEP Trials
1/26/2026
VP of Clinical Development, HIV, Moupali Das shares how the sponsor approaches diverse participant recruitment and enrollment, highlighting the importance of early demographic research and careful, intentional PI selection.
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Confronting "Time Toxicity" In Global Oncology And Rare Disease Trials For Operational Excellence And Patient Retention
1/14/2026
Time is the only truly finite resource in a clinical trial. Consultant Leila Cupersmith discusses how sponsors can better design trials with a lower time burden to boost enrollment, retention, and overall operational excellence.