MedPath

Vital Sign Comparison Between Lifelight and Standard of Care - Development

Completed
Conditions
Vital Signs
Interventions
Device: Vital Signs Measurement
Registration Number
NCT04003662
Lead Sponsor
Xim Limited
Brief Summary

Patients and volunteers both with and without medical problems will be recruited; vital sign measurements are taken twice with normal equipment and while recording video data at the same time. The data collected will allow the Artificial Intelligence to develop the LifeLight algorithm to to improve measurement accuracy of its video data based vital signs monitor.

Detailed Description

Vital signs such as heart rate, blood pressure, breathing rate and oxygen levels currently need several pieces of equipment and trained staff in order to be measured properly. The LifeLight app measures the same vital signs using a camera in a phone, tablet, laptop or smart TV. By using very small changes in the colour of your skin, LifeLight's AI system can calculate these values without any extra equipment or training, and without contact.

The aim of this research study is to improve the accuracy of the LifeLight system with a view to a subsequent Validation study to prove the level of accuracy. The investigators will recruit patients, staff and visitors, both with and without medical problems, and take vital sign measurements twice with normal equipment and while recording video data at the same time. This will allow the AI which develops the LifeLight algorithm to make it more accurate, prior to a subsequent study which will validate the results.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
9000
Inclusion Criteria
  • I1. Sufficiently conversant in the English language to satisfy I3.
  • I2. Able and willing to comply with all study requirements.
  • I3. Able and willing to provide written informed consent to participate (including by parent or legal guardian if under 16 years old).
Exclusion Criteria
  • There are no exclusion criteria.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
inpatientsVital Signs MeasurementVital signs measurement - standard of care and prototype
outpatientsVital Signs MeasurementVital signs measurement - standard of care and prototype
Healthy controlsVital Signs MeasurementVital signs measurement - standard of care and prototype
Primary Outcome Measures
NameTimeMethod
Blood Pressure ReadingsSingle Visit; up to one day

Comparison of digital video data to standard of care measurement

Heart Rate (pulse) ReadingsSingle Visit; up to one day

Comparison of digital video data to standard of care measurement

Respiratory RateSingle Visit; up to one day

Comparison of digital video data to standard of care measurement

Oxygen Saturation ReadingsSingle Visit; up to one day

Comparison of digital video data to standard of care measurement

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Portsmouth Hospitals NHS Trust

🇬🇧

Portsmouth, England, United Kingdom

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