Vital Sign Comparison Between Lifelight and Standard of Care - Development (VISION-D)

Xim Limited

Status: Completed

Conditions: Vital Signs

Treatments: Device: Vital Signs Measurement

Study type: Observational

Funder types: Industry

Identifiers

NCT04003662

PHT/2018/25 IRAS ID 242581

Details and patient eligibility

About

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.

Full 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.

Enrollment: 9,000 patients

Sex: All

Ages: 3+ years old

Volunteers: No Healthy Volunteers

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.

Trial design

9,000 participants in 3 patient groups

inpatients

Description:

Vital signs measurement - standard of care and prototype

Treatment:

Device: Vital Signs Measurement

outpatients

Description:

Vital signs measurement - standard of care and prototype

Treatment:

Device: Vital Signs Measurement

Healthy controls

Description:

Vital signs measurement - standard of care and prototype

Treatment:

Device: Vital Signs Measurement