A Study Of Philips Camera Vital Signs #2

Overview

About this study

The purpose of this research is to systematically assess and validate the capabilities and benefits of the contactless “passive” monitoring system in real-world clinical settings, thereby supporting regulatory clearance and integration into existing healthcare systems to enhance patient monitoring and outcomes.  The project goals and aims are linked together and essentially build off of each previous aim. 

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Adult patients (≥18 years old) admitted to Saint Mary’s Hospital.

  • Patients expected to remain in-room for at least 24 hours during routine monitoring.

  • Patients (or their legal representatives) able and willing to provide informed consent.

 

Exclusion Criteria:

  • Not able to sign consent

  • Pregnancy

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 8/7/2025. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Bruce Johnson

Contact us for the latest status

Contact information:

Jessica Johnston

(507) 266-2696

johnston.jessica1@mayo.edu

More information

Publications

Publications are currently not available