Using mobile devices to measure vital signs and biomarkers from video
Measuring Vital Signs and Biomarkers From Mobile Device Videos
This study tests if mobile devices can accurately measure vital signs and health markers from video in people with cardiometabolic diseases compared to standard medical tools.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 200 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Maiv Health Inc. Industry-sponsored |
| Locations | 1 site (Cedar Park, Texas) |
| Trial ID | NCT06136156 on ClinicalTrials.gov |
What this trial studies
This research investigates the effectiveness of mobile devices in capturing vital signs and biomarkers through video technology, comparing these results to traditional clinical office tools. The study aims to assess the accuracy and reliability of these mobile measurements in patients with cardiometabolic diseases. Participants will be required to remain seated for 30 minutes and undergo a venous blood draw to facilitate the comparison of data collected. The observational nature of the study allows for real-world data collection without intervention.
Who should consider this trial
Good fit: Ideal candidates are individuals with cardiometabolic diseases who can remain seated for 30 minutes and are able to provide a venous blood sample.
Not a fit: Patients with conditions that prevent them from sitting for extended periods or those unable to provide a venous blood sample may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could provide a more accessible and efficient method for monitoring vital signs and biomarkers in patients.
How similar studies have performed: While the use of mobile devices for health monitoring is gaining traction, this specific approach of using video for vital sign measurement is relatively novel and has not been extensively tested in prior studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Must be able to stay in a seated position for 30 minutes * Must be able to participate in a venous blood draw Exclusion Criteria: * Condition that prevents prolonged seated position * Condition that restricts ability to provide venous blood sample
Where this trial is running
Cedar Park, Texas
- ARCpoint Labs of Cedar Park — Cedar Park, Texas, United States (Recruiting)
Study contacts
- Principal investigator: Sandro Luna, MD — Maiv Health Inc.
- Study coordinator: Sandro Luna, MD
- Email: team@maivhelalth.com
- Phone: 5125932378
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.