Reduce dropout. Reduce coordinator burden. Without adding compliance risk.
Clear Trials gives IRBs, Site Networks, CROs, and Sponsors a tool to support participant comprehension throughout the trial—not just at consent. Plain-language summaries that help participants stay informed, prepared, and enrolled.
The comprehension gap
Documents meet requirements. Participants still struggle.
Consent forms meet regulatory requirements. They also average a 10th-14th grade reading level—while most adults read at a 7th-8th grade level.
The result: participants sign documents they don't fully understand, then struggle with visit schedules, medication rules, and preparation instructions throughout the trial.
This isn't a document problem. It's a support problem that continues long after consent.
The opportunity
Support participant comprehension as part of your services.
Clear Trials transforms approved consent forms and trial documents into plain-language summaries—without changing meaning, minimizing risks, or adding claims. Our AI-powered system uses strict guardrails fully vetted by IRB partners, operating in a contained environment unlike generic LLMs. Every output is editable, includes complete audit trails, and is fully reviewable by humans before participants ever see it.
As a partner, you can:
- Offer Clear Trials to your sites, sponsors, or network as a value-added service or standard offering
- Review and approve simplified outputs before they reach participants, maintaining full control
- Differentiate your organization with tools that support informed consent and participant retention beyond the signature
- Reduce coordinator burden by giving participants 24/7 access to clear trial information
- Improve retention metrics by supporting participant comprehension throughout the trial journey
You stay in control. We provide the infrastructure.
What we never do.
Add claims that aren't in the source document
Minimize risks or side effects
Use promotional language
Provide medical advice
Remove uncertainty language
Alter voluntary participation framing
We simplify. We don't spin.
Simple to integrate. Nothing to disrupt.
You review
We generate plain-language versions of approved documents using IRB-vetted guardrails. You review, edit if needed, and see complete audit trails before anything reaches participants.
Participants access
Coordinators or study staff provide participants with access codes at enrollment. Participants see simplified versions alongside official documents, accessible 24/7.
Participants engage
24/7 access to clear explanations of their trial. Questions get answered before they become phone calls—or dropouts.
You see the impact
Aggregate comprehension and engagement metrics across your organization. No individual participant data shared without consent.