Connected recovery infrastructure, starting with stroke
Turn home rehabilitation into a visible, connected pathway.
REGAIN connects the programme prescribed by a clinician with the person doing the work, the people supporting them and the evidence needed to improve what happens next.
- Origin
- Research-led
- Design
- Lived experience
- Intelligence
- FASTlab architecture
Research foundationUniversity of Newcastle · HMRI · ARC Connected Sensors for Health
Stroke population: Australian Commission on Safety and Quality in Health Care, June 2026. Capital range is a planning scenario subject to final scope and quotation.
The opportunity
A rehabilitation workflow—not another exercise library.
REGAIN is being designed as the connective layer between clinical intent and recovery at home: accessible practice, structured reflection, appropriate support and evidence that can inform the next human decision.
Executive summary
The missing layer after discharge.
Home rehabilitation is where repetition, confidence and everyday support matter most—yet it is also where the pathway becomes hardest to see. REGAIN aims to make that work easier to follow and more useful to everyone around recovery.
Where the pathway goes dark
Conceptual illustration, not measured dataThe programme travels. The pathway does not.
Instructions, videos, appointments and family support often sit apart rather than operating as one coherent experience.
What happens at home is difficult to understand.
Attendance alone cannot explain confidence, fatigue, pain, difficulty or the context surrounding participation.
Care circles are important but poorly equipped.
Family and friends need a useful role that supports recovery without shifting clinical responsibility onto them.
Investment thesis
Build the connective workflow, prove value in stroke, then license the pathway.
- Clear wedge
- Clinician-prescribed rehabilitation activated for use at home.
- Multi-sided value
- A simpler experience for survivors; bounded support for carers; structured visibility for services.
- Expandable architecture
- Potential pathway profiles for frailty, falls, orthopaedic and neurological recovery after validation.
- Compounding asset
- Governed evidence about what works, for whom, in what context and with what confidence.
Platform
One loop around the person recovering.
The proposed MVP connects five actions without attempting to automate care.
Accessible guided activities.
Your home programme is ready
Set by your physiotherapist for this week.
Scan the code from your clinic
Ball roll
How did this week feel?
Your programme has changed
Your physiotherapist reviewed your check-in and adjusted next week's activities.
“I just want to get back to my Tuesday craft group.”Meet Margaret · composite character, illustrative scenario
Guidance without friction
Large controls, captions, voice support, carer-assisted onboarding and pathways that do not assume an email address.
REGAIN is currently conceived as a rehabilitation resource companion. It is not a medical device, does not diagnose or direct treatment and does not replace clinical care.
Market
A large need. A deliberately narrow entry point.
More than 440,000 Australians live with the effects of stroke. REGAIN’s initial commercial focus is not every survivor: it is the organisations responsible for extending rehabilitation into the home.
Demonstrates the scale of persistent need; it is not presented as obtainable revenue.
Organisations with a defined cohort, clinical workflow and need for visibility beyond appointments.
The first commercial objective: paid, evidence-generating deployments—not premature national scale.
Commercial model
Organisation-funded access is the leading hypothesis.
The pilot will test who buys, what they value and which unit of pricing best matches procurement. The figures below are commercial scenarios, not contracted prices or forecasts.
Provider licence
A service deploys REGAIN to a defined cohort and pays for the platform, onboarding and evidence reporting.
- Activation or cohort-based access
- Implementation support
- Evidence and value reporting
- Annual renewal pathway
Indicative commercial test per site.
Working hypothesis per active patient annually.
Validation and moat
The product improves by making reasoning visible.
REGAIN sits as an application profile within FASTlab’s Evidence Intelligence stack. The architecture governs how activity becomes meaning, how confidence is expressed and how learning is retained.
The defensible layer
Most platforms collect data. REGAIN is designed to govern what happens next.
FASTlab Evidence Intelligence Architecture™ Stage 1 of 7
Define what must be understood before deciding what data is relevant.
Refine the POC
Complete workflows and accessibility design.
Output: testable experienceStakeholder testing
Test with survivors, carers and clinicians.
Output: usability evidenceStructured pilot
Test engagement, workflow and buyer value.
Output: adoption evidenceFirst paid deployment
Convert learning into a repeatable offer.
Output: revenue evidenceInvestment ask
Capital tied to evidence-producing milestones.
The immediate objective is to finish the product definition, secure a precise build pathway and fund validation toward first revenue. The final raise structure follows the completed POC and development quotation.
Indicative range only, subject to final scope and a precise development quotation.
Planning range for product completion, validation, evidence development and first-market preparation.
Use of funds
Dollar ranges apply the allocation to the $350k–$500k scenarioAccessible workflows, security and core data model.
$122.5k–$175kStakeholder testing and structured pilot delivery.
$87.5k–$125kMeasures, interpretation and buyer reporting.
$70k–$100kPricing, procurement and first-customer development.
$70k–$100kAllocation is illustrative and will be revised against the final build scope. Preferred capital adds healthcare knowledge, implementation access or commercialisation capability—not cash alone.
Capability
A venture coalition built around translation.
The opportunity draws together rehabilitation expertise, lived experience, product development and FASTlab’s design-and-evidence capability. Formal ownership and venture structure remain intentionally undecided.
Rehabilitation expertise
Shapes relevance, safety boundaries and workflow fit.
Survivors and carers
Shape accessibility, motivation and the realities of use at home.
FASTlab
Originates the experience design, validation pathway and Evidence Intelligence architecture.
Devika
Developing the proof of concept and informing the route to build.
Research provenance
REGAIN has emerged from research and development involving the University of Newcastle and Hunter Medical Research Institute, supported through the ARC Research Hub for Connected Sensors for Health.
- Research and development involvingUniversity of Newcastle
- Research and development involvingHunter Medical Research Institute
- Supported throughARC Research Hub for Connected Sensors for Health
This provenance establishes the research foundation of the work. It does not imply institutional endorsement of, ownership in, investment in, or commitment to the proposed commercial venture.
Structure
Designed before it is divided.
The investment case does not imply a settled ownership arrangement between REGAIN, FASTlab or future participants. Company, IP, licensing and equity arrangements must be agreed before external investment.
| Risk | De-risking action |
|---|---|
| Product adoption | Stakeholder testing before final build |
| Clinical boundary | Human-led workflow and explicit product limits |
| Buyer and pricing | Paid pilot and procurement discovery |
| Venture structure | Resolve ownership and IP before investment |
| Pathway expansion | Validate each application profile independently |
REGAIN investment proposition
Make recovery at home visible enough to support—and valuable enough to scale.
The next value-inflection point is a validated POC, a costed MVP and a credible path to the first paid deployment.