Validated in the US and proven globally

Across multiple studies and care settings in Australia, New Zealand, the UK, and Canada, PainChek® has consistently delivered measurable clinical outcomes:

  • Medication optimization: Reduced use of analgesics, antipsychotics, antidepressants, anxiolytics, and hypnotics
  • Resident well-being: Improved nutrition, increased mobility, reduced dependency, and improved quality of life
  • Safety and care quality: Fewer falls, reduced distress, and improved staff confidence in pain assessment
  • Operational benefits: Improved care efficiency and significant cost savings

In a pivotal clinical trial in the US, PainChek® demonstrated strong agreement with the internationally recognized Abbey Pain Scale, delivering accurate pain intensity assessments and reliable performance across diverse resident demographics and device platforms.

Interested in implementing PainChek® in your facility?

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Find out how PainChek® can support your organization.

Request a demo today or call 1 800 720 7504.

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PainChek® meets regulatory standards for use in Australia, New Zealand, Canada, Singapore, Malaysia, the United Kingdom, the European Union, and PainChek® Adult has been granted a De Novo classification by the US Food and Drug Administration (FDA) for its PainChek® Adult App. The FDA De Novo Grant number is DEN240073. The tool is included in the Australian Register of Therapeutic Goods (ARTG) under ARTG number 302794.

PainChek® is a registered trade mark of PainChek in Australia, the United Kingdom, the European Union, and a trade mark in other jurisdictions.

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