NCT06136156

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
237

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2023

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 17, 2023

Completed
14 days until next milestone

Study Start

First participant enrolled

October 31, 2023

Completed
18 days until next milestone

First Posted

Study publicly available on registry

November 18, 2023

Completed
1.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 4, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 4, 2025

Completed
Last Updated

September 29, 2025

Status Verified

September 1, 2025

Enrollment Period

1.8 years

First QC Date

October 17, 2023

Last Update Submit

September 26, 2025

Conditions

Cardiometabolic Diseases

Outcome Measures

Primary Outcomes (4)

  • Heart rate in beats per minute

    2 minutes

  • Blood pressure (systolic/diastolic) in millimeters of mercury (mmHg)

    2 minutes

  • Respiration rate in breaths per minute

    2 minutes

  • Oxygen saturation in SpO2 percentage

    2 minutes

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

You may qualify if:

  • Must be able to stay in a seated position for 30 minutes
  • Must be able to participate in a venous blood draw

You may not qualify if:

  • Condition that prevents prolonged seated position
  • Condition that restricts ability to provide venous blood sample

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

ARCpoint Labs of Cedar Park

Cedar Park, Texas, 78613, United States

Location

Study Officials

  • Sandro Luna, MD

    Maiv Health Inc.

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
INDUSTRY
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

October 17, 2023

First Posted

November 18, 2023

Study Start

October 31, 2023

Primary Completion

September 4, 2025

Study Completion

September 4, 2025

Last Updated

September 29, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

Locations

US(1)