- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06136156
Video Vitals and Biomarkers
November 14, 2023 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
Recruiting
Study Type
Observational
Enrollment (Estimated)
200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Sandro Luna, MD
- Phone Number: 5125932378
- Email: team@maivhelalth.com
Study Locations
-
-
Texas
-
Cedar Park, Texas, United States, 78613
- Recruiting
- ARCpoint Labs of Cedar Park
-
Contact:
- Sandro Luna, MD
- Phone Number: 512-593-2378
- Email: team@maivhealth.com
-
-
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
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 (Estimated)
September 30, 2024
Study Completion (Estimated)
September 30, 2024
Study Registration Dates
First Submitted
October 17, 2023
First Submitted That Met QC Criteria
November 14, 2023
First Posted (Estimated)
November 16, 2023
Study Record Updates
Last Update Posted (Estimated)
November 16, 2023
Last Update Submitted That Met QC Criteria
November 14, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- AX8
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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