Video Vitals and Biomarkers

September 26, 2025 updated by: Sandro Luna, Maiv Health Inc.

Measuring Vital Signs and Biomarkers From Mobile Device Videos

The investigators are doing this research to study the ability of mobile devices to measure vital signs and biomarkers from video as compared to standard-of-care clinical office tools.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

237

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • Texas
      • Cedar Park, Texas, United States, 78613
        • ARCpoint Labs of Cedar Park

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

Adults greater than 18 years old may participate in this research study

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Heart rate in beats per minute
Time Frame: 2 minutes
2 minutes
Blood pressure (systolic/diastolic) in millimeters of mercury (mmHg)
Time Frame: 2 minutes
2 minutes
Respiration rate in breaths per minute
Time Frame: 2 minutes
2 minutes
Oxygen saturation in SpO2 percentage
Time Frame: 2 minutes
2 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Maiv Health Inc.

Investigators

  • Principal Investigator: Sandro Luna, MD, Maiv Health Inc.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 31, 2023

Primary Completion (Actual)

September 4, 2025

Study Completion (Actual)

September 4, 2025

Study Registration Dates

First Submitted

October 17, 2023

First Submitted That Met QC Criteria

November 14, 2023

First Posted (Actual)

November 18, 2023

Study Record Updates

Last Update Posted (Estimated)

September 29, 2025

Last Update Submitted That Met QC Criteria

September 26, 2025

Last Verified

September 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • AX8

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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