Clinical trial information, clearly explained.
Clear Trials transforms complex consent forms and protocols into plain language—so participants understand their trial and trial teams spend less time answering the same questions.
Participants don't drop out because of the medicine. They drop out because the job of participating is too hard.
That reframe is what makes Clear Trials different—we're not just simplifying documents, we're building the only platform purpose-built around the full job of being a clinical trial participant.
The cost of participants who find the job of participating too hard.
Consent forms average a 12th-grade reading level. Only 12% of U.S. adults read at that level. The result: participants who don't understand their trial leave it.
average cost to replace a single dropped participant
higher dropout when participants don't understand consent
of coordinators consider their workload excessive
Sources: 12th-grade/12% — readability studies; NAAL; $19.5K — Tufts CSDD; 2.2x — PMC meta-analysis on ICF comprehension; 78% — BMC Health Services Research 2025
Retain participants. Reduce coordinator burden. Deliver on time.
Clear Trials reduces repetitive participant questions, improves comprehension, and helps you retain more patients through the last visit.
Retain more participants
Participants who understand their trial are 2.2x less likely to drop out. Clear Trials simplifies consent forms to a 6th–8th grade reading level and keeps information accessible throughout the trial.
2.2x — PMC meta-analysis on ICF comprehension
Reduce coordinator burden
Coordinators spend 15–30% of their time answering the same participant questions. Clear Trials gives participants 24/7 access to answers sourced directly from their trial documents.
15–30% — ACRP industry surveys
Deliver on time and budget
Fewer dropouts mean fewer costly re-recruitments. 80% of sponsors prefer smaller CROs for flexibility—Clear Trials gives you a retention tool that turns your size into an advantage.
80% — Applied Clinical Trials survey
The full job of participating—supported.
Plain-language summaries, timelines, and answers. Participants can share access with family or caregivers—a differentiator that helps support networks stay informed. Designed to preserve key information, including risks, without adding promotional content. Always pointing back to official documents and the study team.
Orient to the study
Plain-language synthesis of consent forms and protocols—understand what you're signing up for
Know what's coming next
Timeline and visit preparation—so you're ready before you arrive
Get answers when they come up
Semantic search across your documents—24/7, sourced from your actual trial materials
Reach the right person
Study contacts directory—know who to call for what
Involve your support system
Caregiver access and sharing—the people helping you can see the same information
Find support beyond the trial
Curated study resources—connect with what you need
A coordinator can hand-hold 20 participants. They can't hand-hold 200.
As trials get larger and more decentralized, the old model breaks. Clear Trials delivers retention and efficiency from one platform, one implementation—no linear headcount scaling.
Live in weeks, not quarters.
AI guardrails designed in consultation with IRB professionals. Full audit trails. You stay in control.
Unlike generic LLMs, Clear Trials operates within strict, contained boundaries. Every output is editable, includes complete audit trails, and is fully reviewable before participants ever see it.
- Nothing reaches participants without your explicit approval
- Complete audit trails for every document transformation
- HIPAA-compliant infrastructure, no PHI in the application database
- Designed to support ICH-GCP compliance from the ground up