Understand consent
Get study terminology explained before the consent conversation, not after.
Industry
What participants can do with Lunas today: understand the documents, organize the records, keep the story straight across visits.
The opportunity
A twenty-page consent form does its legal job and fails its human one: the person signing it still wants to know, in plain terms, what "randomized" means for them and which symptoms they're supposed to report. Between visits, the screening labs and visit summaries pile up like everyone else's medical paper.
A participant with a Lunas account can upload those documents and ask. Stethos explains the terminology without replacing the official material or the consent conversation — and it helps the person write down the questions they actually want the coordinator to answer. Lab results from the study join the same confirmed, charted record as everything else.
Coordinator dashboards and protocol-specific workspaces are roadmap; today's value is a participant who understands more and loses less.
Where Lunas fits
Stethos helps explain, organize, and investigate. People and qualified professionals stay responsible for the decisions that follow.
Get study terminology explained before the consent conversation, not after.
Arrive at visits with the questions that matter written down.
Screening labs and visit documents build one continuous history.
Grant access to specific records and revoke it when the study ends.
A practical workflow
A repeatable path makes the model easier to supervise and the result easier to trust.
Consent forms, instructions, and results go into the participant's account.
Stethos explains terms and flags what's worth asking the study team.
Confirmed values chart over the course of the study.
Eligibility, safety, and protocol calls stay with investigators and staff.
Product path
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
Team, Enterprise & API direction
Questions
No. Informed consent is a process owned by the study team, with approved documents and a real conversation. Lunas can help a person understand the language beforehand and prepare questions — which tends to make that conversation better, not replaceable.
No. Eligibility is decided by the investigator against the protocol. Lunas can help you organize the records and history a screening visit will ask about, so the people who do decide have what they need.
Not yet. There are no team workspaces or study-platform integrations today — those are roadmap. What exists is the individual product, which participants can choose to use for their own understanding and records.
Try the product
Use Lunas for information and organization, then involve a qualified professional whenever a health decision is needed.