01
Participant education
Translate approved study concepts into clearer language without changing the official material.
Industry
Studies
Clearer participant information, organized study context, and human-reviewed medical AI assistance across the study journey.
What Lunas supports
- Participant-friendly explanations of approved material
- Organized submissions and longitudinal context
- Clear handoff to investigators and study staff
The opportunity
Why this work needs medical context
Participants face long consent documents, unfamiliar terminology, repeated instructions, and uncertainty about which questions belong with the study team. Staff face the reverse problem: fragmented information that must be reviewed consistently and according to protocol.
Lunas can make both sides easier to navigate. Stethos can explain approved text and help structure a person’s question, while the study team remains responsible for consent, eligibility, adverse events, and protocol interpretation.
Where Lunas fits
Useful work before the final decision
Stethos helps explain, organize, and investigate. People and qualified professionals stay responsible for the decisions that follow.
02
Question preparation
Help participants identify what they want the investigator or coordinator to explain.
03
Submission context
Organize permitted files, notes, and observations for the study team’s review.
04
Longitudinal follow-up
Keep study-related context understandable across visits and time points.
A practical workflow
From a question to human review
A repeatable path makes the model easier to supervise and the result easier to trust.
- 01
Approve the boundaries
Define the official content, protocol constraints, consent language, and escalation path.
- 02
Support understanding
Use Lunas to explain terms and prepare questions without replacing informed consent.
- 03
Structure information
Collect the permitted context in a consistent, reviewable form.
- 04
Investigator decides
Study staff review source information and make all protocol, eligibility, and safety decisions.
Product path
Start with Lunas today. Grow into governed workflows.
Lunas.One is available to individuals today. Team & Enterprise workspaces and a governed Stethos API are in active development — the roadmap below is directional, not a promise of present availability, and larger deployments will require the right privacy, security, evaluation, and human-review controls.
Available in Lunas
- Individual file-aware conversations
- Lab projects and longitudinal record foundations
- Controlled collaboration and audit-oriented access patterns
Team, Enterprise & API direction
- Study team workspaces and role administration
- Protocol-specific approved knowledge and templates
- Governed study-platform integrations
Questions
What people usually want to know
Can Lunas obtain informed consent?
No. It can help a person understand terms and prepare questions, but the approved consent process and responsible study team remain essential.
Can Lunas decide whether someone qualifies?
No. Eligibility decisions belong to the investigator and protocol-defined process.
Could it support observational and clinical studies?
The organizational and education patterns may help both, but every deployment needs study-specific privacy, consent, protocol, regulatory, and validation review.
Try the product
Bring one real health question into context.
Use Lunas for information and organization, then involve a qualified professional whenever a health decision is needed.