Frequently Asked Questions

Hyper‑Care is a community‑driven health intelligence platform that helps patients and communities organize health data, participate in research, and generate real‑world evidence to improve care and accelerate innovation

Our mission is simple: Empowering Patients & Advancing Care - We aim to give patients control of their data and create shared value for their contributions

Patients, caregivers, advocacy groups, researchers, and healthcare organizations can all participate. We focus on rare, chronic, and under‑served conditions, but the platform is adaptable to many health areas

Patients connect their health data (medical records, devices, surveys) through secure consent. Communities organize into living registries that enable research, clinical trial matching, and real‑world evidence generation

Both. It’s a patient‑first platform designed to support community engagement and research readiness, including trial recruitment, outcomes tracking, and evidence generation

We use the latest HIPAA‑aligned security, encryption, zero-knowledge cryptography, granular consent, and transparent governance. You decide what data to share, with whom, and for what purpose

Not without your consent - Your data - Your control - Your compensation

Medical records, lab results, wearable/device data, patient‑reported outcomes, and claims or genomic data - always under your control

Patients are compensated for contributing to research - but also gain early access to promising therapies, condition insights, & safe technology to navigate their healthcare journey

Communities can accelerate research, drive sustainable funding, and influence care guidelines by organizing high‑quality, longitudinal, condition specific data

Yes - Patients and caregivers can join at no cost

We help sponsors and CROs find pre‑qualified cohorts, streamline eligibility checks, and enable decentralized workflows like eConsent and ePROs

Absolutely - Rare and complex conditions are a core focus - We work with advocacy groups to build active registries and trial‑ready cohorts

We combine patient‑reported measures, device streams, and clinically linked data with standard terminologies and provenance tracking for research‑grade datasets

Yes - We use standards‑based interoperability (FHIR) so patients can connect their records and share insights with providers they choose

Yes - We enable remote consent, telehealth integration, and digital endpoints to reduce site burden and improve access

We use strong 3 factor identity verification and granular consent controls, so you can manage participation across multiple organizations & studies, without repeated friction

Hyper‑Care is community‑centric and research‑grade from day one - It’s not just about tracking health - it’s about turning patient data into actionable evidence for better care

Once a community registry is live, we can screen, notify, and enroll participants rapidly, reducing delays and improving diversity

Yes. We capture clinical, patient‑reported, and real‑world outcomes to support regulatory submissions, coverage decisions, and quality improvement

By providing real‑world insights and patient‑reported measures, we help close gaps in care and support value‑based coverage

No - Hyper‑Care is a Public Benefit Corporation (P.B.C.), which means we operate for profit but prioritize public benefit alongside shareholder value

We commit to transparent value exchange through revenue sharing with communities and their members

Yes - Patients can connect genomic data from labs or prior tests to enrich research and natural‑history studies

Create an account, and connect your health data - Join patient communities which support your condition