female patient with tablet

Propel Your Trial Forward with Built-in Participant Engagement.

Participant engagement in clinical trials directly impacts retention, data quality, and study timelines. At YPrime, we approach participant engagement as a foundational part of trial execution—not a standalone add-on.

Our built-in participant engagement, embedded within YPrime’s eCOA platform, helps sponsors and CROs reduce participant burden, minimize dropout risk, and keep trials moving forward with certainty.

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Built-in Participant Engagement
Are Participant Dropouts Impacting Your Clinical Trial Success?

30% of
patients drop
out of trials

Leading to missed endpoints and delayed timelines.1

$19,000 for
each
replacement

The true cost of recruitment and re-enrollment.1

80% of trials
delayed by
~one month

Many delayed significantly longer1

Embed Participant Engagement.
Improve Retention.

YPrime’s approach to participant engagement is grounded in behavioral research and real-world trial execution. By embedding engagement directly into our eCOA platform, we help participants feel informed, prepared, and supported throughout their study participation.

bullet icon imageEngagement is embedded directly into the assessment experience, without requiring additional apps, portals, or fragmented workflows.
bullet icon imageMultilingual support, clear navigation, and thoughtful notifications support diverse participant populations across regions.
bullet icon imageInteractions are designed to reduce anxiety, encourage timely completion, and support sustained participation over time.

With YPrime, participant engagement is not a feature—it is an integrated strategy to protect data integrity, improve retention, and support trial success.

Improve Clinical Trial Retention with the YPrime Participant Hub.

Built directly within the YPrime eCOA platform, the Participant Hub provides participants with centralized access to study guidance, upcoming activities, and key resources throughout the trial. At the center of the experience is the “For You” Page, which organizes visit schedules, study information, and protocol guidance within the eCOA app—helping participants stay informed and engaged while reducing participant burden. 

Key capabilities include: 

bullet icon imageCentralized Study Information – Visit schedules, study explanations, and key resources in one location
bullet icon imageTask Visibility – Clear view of upcoming assessments and study activities
bullet icon imageProtocol Guidance – FAQs, training materials,  approved study documentation, and more 

Improve Clinical Trial Retention with the
YPrime Participant Hub.

Built directly within the YPrime eCOA platform, the Participant Hub provides participants with centralized access to study guidance, upcoming activities, and key resources throughout the trial. At the center of the experience is the “For You” Page, which organizes visit schedules, study information, and protocol guidance within the eCOA app—helping participants stay informed and engaged while reducing participant burden. 

Key capabilities include: 

bullet icon imageCentralized Study Information – Visit schedules, study explanations, and key resources in one location
bullet icon imageTask Visibility – Clear view of upcoming assessments and study activities
bullet icon imageProtocol Guidance – FAQs, training materials,  approved study documentation, and more 
Get Started
YPrime’s clinical trial technology platform offers patient engagement features across eConsent and eCOA, leveraging user-friendly design, personalization, and behavioral science to drive patient retention and adherence.
Nisarg Shah, Practice Director, Everest Group
Woman working on a tablet, representing patient engagement through human-centric clinical trial technology focused on user experience and daily life integration

Participant Engagement
with Certainty—We’ve
Got You Covered.

Before they are trial participants, people bring questions, concerns, and real-life responsibilities into every study. YPrime’s participant engagement strategy is built on this understanding.

Through human-centric design and research-informed decision-making, we focus on reducing participant burden and uncertainty by delivering clear, relevant information at every stage of the trial. By integrating engagement directly into the clinical trial workflow, studies fit more naturally into participants’ daily routines, supporting adherence, retention, and overall trial performance.

Let YPrime Help You Run Your Clinical Trials with Certainty.

When we work together, you gain confidence that your clinical trial technology supports participants, sites, and sponsors alike. YPrim eConsent, IRT, and eCOA enables informed participation, operational consistency, and inspection-ready execution across global trials.

Explore Insights from Our Experts.

Gain practical perspectives on participant engagement, clinical trial design, and technology-enabled execution—so you can make confident decisions throughout the study lifecycle.

Sources

  1. The True Cost Of Patient Drop-outs In Clinical Trials
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