The purpose of this study is to collect and assess feedback from the users regarding the functionality and performance of the Portrait Mobile Monitoring Solution V2.0. In addition, this study aims to collect raw parameter data from the investigational devices for use in current and future Portrait Mobile development, including engineering purposes as deemed appropriate by the Sponsor.
Subjects will be enrolled from a general hospital ward to receive continuous monitoring for up to 72 hours by the Portrait Mobile Monitoring Solution V2.0. After the completion of that monitoring, both the clinician and the subject will complete a feedback survey about their experience with the device. The surveys along with raw data from the device will be collected from each subject.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
50
Subjects will have vital signs continuously monitored for up to 72 hours with the study device
West Middlesex University Hospital
London, England, United Kingdom
Collection of user feedback surveys from Clinicians
Number of clinician feedback surveys collected at the end of each shift for clinicians overseeing care of subjects receiving continuous vital signs monitoring.
Time frame: Up to 72 hours
Collection of Subject Survey
Number of subject surveys collected from study participants at the end of their continuous monitoring
Time frame: up to 72 hours
Collection of raw parameter data from Portrait Mobile Device
Collection of electronic waveforms and device logs from the investigational device for the entire monitoring period for each subject.
Time frame: up to 72 hours
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