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Clinical Trials/NCT04003662
NCT04003662CompletedNot Applicable

Vital Sign Comparison Between Lifelight and Standard of Care - Development

Xim Limited1 site in 1 country9,000 target enrollmentStarted: May 1, 2018Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
9,000
Locations
1
Primary Endpoint
Blood Pressure Readings

Study Overview

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.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
3 Years to — (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Sufficiently conversant in the English language to satisfy I
  • Able and willing to comply with all study requirements.
  • 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.

Outcomes

Primary Outcomes

Blood Pressure Readings

Time Frame: Single Visit; up to one day

Comparison of digital video data to standard of care measurement

Heart Rate (pulse) Readings

Time Frame: Single Visit; up to one day

Comparison of digital video data to standard of care measurement

Respiratory Rate

Time Frame: Single Visit; up to one day

Comparison of digital video data to standard of care measurement

Oxygen Saturation Readings

Time Frame: Single Visit; up to one day

Comparison of digital video data to standard of care measurement

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Xim Limited
Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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