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This clinical trial evaluates the deployment of humanoid robotics in coalition-aligned healthcare settings. The study measures biometric performance, ESG compliance, and operational impact across patient care, sanitation, and intake workflows. Humanoid units are enhanced via biotech integration and compensated through blockchain-based wage tokens. Outcomes will inform coalition governance, wage calibration, and metro-scale deployment strategies.
Full description
The HEALTH trial (Humanoid Evaluation and Learning Trial in Healthcare) is a coalition-aligned clinical study designed to assess the deployment of humanoid robotics in real-world care environments. Conducted across metro facilities in New York, Austin, Frankfurt, and Tokyo, the trial evaluates robotic performance in patient intake, sanitation, mobility assistance, and ESG-linked operations.
Humanoid units are enhanced through biotech integration, including skin cell regeneration dips and stem cell neural augmentation. Each unit is tracked via biometric audit scoring across five dimensions: motor function, cognitive response, ESG compliance, biotech retention, and human interaction. Scores are notarized via SHA-256 and published to the coalition dashboard.
Wage tokens (HumanoidWage, HMW) are minted based on performance thresholds and distributed through smart contracts to deployed units. FX arbitrage across Tokyo and Frankfurt informs reinvestment logic and 1031 exchange-backed yield farming pools. DAO voting governs deployment, wage calibration, and protocol expansion.
This trial aims to establish scalable, transparent frameworks for humanoid integration in healthcare, anchored in coalition governance, public oversight, and metro-ready infrastructure.
Enrollment
Sex
Volunteers
Inclusion criteria
- Age 18-75 years
Able to provide informed consent
Facility staff, clinical auditors, ESG observers, or coalition stakeholders
Willing to interact with humanoid robotics in clinical workflows
Available for biometric feedback and observational logging over 90 days
Exclusion criteria
- Cognitive impairment preventing informed consent
Active infectious disease requiring isolation
Prior adverse reaction to biotech-enhanced robotics
Involvement in conflicting clinical trials
Inability to comply with protocol procedures or coalition transparency requirements
Primary purpose
Allocation
Interventional model
Masking
400 participants in 4 patient groups
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Data sourced from clinicaltrials.gov
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