FOR HEALTHCARE PROVIDERS
Designed to support patient engagement between visits.
CardiFit is being developed as a focused patient-support layer for cardiac rehabilitation—built to respect clinical judgment, defined responsibility, and the realities of existing workflows.
THE WORKFLOW CHALLENGE
A plan can be clinically sound and still be difficult to carry into daily life.
Between visits, patients interpret instructions, remember routines, make choices, and decide when to ask for help. Digital support is useful only if it helps without creating undefined responsibility for the clinical team.
INTENDED ROLE
Support approved care, do not redefine it.
CardiFit is intended to help present approved guidance, collect relevant patient input, offer appropriate daily support, and share permitted information with the right participant when responsibilities are defined.
INTENDED SUPPORT LOOP
A bounded model for between-visit support.
Approved context
Start from the guidance and role definitions established by the care arrangement.
Relevant patient input
Ask for only the information needed for the approved experience.
Appropriate daily support
Offer reminders, prompts, education, and reflection within defined boundaries.
Permitted information
Route information only to the participant who is authorized and responsible for receiving it.
RESPONSIBILITY AND ESCALATION
The hard questions must be answered before implementation.
Who reviews which information—and on what schedule?
- What is informational rather than actionable?
- How are response expectations communicated to patients?
- What happens when information falls outside the program’s role?
- How are emergency boundaries made unmistakable?
ACCOUNTABLE SUPPORT
Development priorities, not unverified achievements.
Anthogen is treating explainability, versioning, accessibility, privacy, security, safety review, and human oversight as development priorities. Public claims about these areas require evidence and approval.
WHAT ANTHOGEN MUST DEMONSTRATE
Usefulness has to work in the real workflow.
Patients can understand and use the experience
- Support remains within approved clinical and product boundaries
- Roles and escalation paths are explicit
- Information is relevant and appropriately permissioned
- Implementation requirements are practical and measurable
IMPLEMENTATION AND EVIDENCE
Evaluate the questions before making the claims.
The Evidence & Development page sets out the product, clinical, workflow, privacy, security, and evidence questions Anthogen is working to answer.
PRODUCT TOUR
See the intended patient experience in context.
The tour is structured to label approved current screens separately from work in testing or planned.