Algorithm Verification
Conditions
Brief summary
This single center prospective clinical study is to verify the algorithm of mCVI® in 4 different lighting conditions to accurately capture pulse rate and respiratory rate in 10 healthy subjects in comparison to commercially-available Masimo pulse oximeter devices. This is a non significant risk device.
Detailed description
In this prospective clinical study the mCVI® device is a mobile application used to simply verify the algorithm when the mobile video reads a patients pulse rate and respiratory rate while spontaneously breathing. There is no facial recognition technology. There is no immediate feedback given to the research team to act upon or provide for further clinical care decisions. In real time, the mCVI® device will be compared to two commercially-available Masimo pulse oximeter devices in a single visit.
Interventions
OTHERThere is no intervention
There is no intervention
Sponsors
Intelomed, Inc.
Study design
Observational model
FAMILY_BASED
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
21 Years to 70 Years
Healthy volunteers
Yes
Inclusion criteria
* Healthy adults between the ages of 21 - 70 * Informed consent obtained and signed
Exclusion criteria
* Self-reported medical conditions that could compromise a participant's ability to provide for all breathing samples, pedal the Cubii Pro elliptical, or follow instructions * Self-reported medical history of respiratory or cardiovascular disease * Excessive facial hair, facial deformities, or obstructions (like glasses or face masks/shields) that could compromise the recording of pulse rate and respiratory rate of the mCVI® * Any face lotions or make up foundations that could compromise the recording of pulse rate and respiration rate of the mCVI® * Missing digits or fingers on one or more hand that would prevent proper recording of Masimo pulse oximeter devices * Participants wearing nail polish, acrylic nails, or rings on the ring finger of either hand that would prevent the proper use of Masimo pulse oximeter device * Inability to provide informed consent
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pulse Rate Verification in Different Lighting Conditions | 2 months | To demonstrate that in 4 different lighting environments common to home and office/clinical conditions, mCVI® accurately captures pulse rate in comparison to Masimo pulse oximeter devices. |
| Respiration Rate Verification in Different Lighting Conditions | 2 months | To demonstrate that in 4 different lighting environments common to home and office/clinical conditions, mCVI® accurately captures respiratory rate in comparison to Masimo pulse oximeter devices. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Skin Tone Pulse Rate Verification in Different Lighting Conditions | 2 months | To demonstrate that in 4 different lighting environments common to home and office/clinical conditions, mCVI® accurately captures pulse rate in healthy volunteers with a variety of skin tones using the Fitzpatrick Skin Type Scale. |
| Skin Tone Respiratory Rate Verification in Different Lighting Conditions | 2 months | To demonstrate that in 4 different lighting environments common to home and office/clinical conditions, mCVI® accurately captures respiration rates in healthy volunteers with a variety of skin tones using the Fitzpatrick Skin Type Scale. |
Countries
United States
Outcome results
None listed