Can your Phone's camera check your pulse? new study says maybe.

NCT ID NCT05853380

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested whether a web-based app can measure pulse rate as accurately as a standard ECG machine. 86 adults aged 22-85 had their pulse measured by both the app and an ECG device at the same time. The goal was to see if the app is accurate enough for everyday use.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Web-based application (Informed Vital Core App) for pulse rate measurement
What this could lead to
If successful, this could provide a convenient, app-based way to check pulse rate without special equipment.
What could go wrong
This is a small, completed study (86 people) focused on accuracy, not treatment. The app may not work as well in real-world conditions or for people with certain skin features.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

86 people

The number who actually took part.

Started

Jun 2023

Finished

Jun 2023

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study will recruit subjects from clinics and hospitals and the general public. Enrollment of 85 subjects with an age range of 22-85 years of age with a wide range of skin tone categorization per the Fitzpatrick Scale ranging from 1-6.

Ages

22 to 85 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Subjects 22 -85 years of age * Subjects willing to sign the Informed Consent Form and comply with the protocol Exclusion Criteria * Subjects required to wear mask or bandage that obstructs forehead, cheeks, or chin * Refusal to remove makeup , sunscreen, lotion, clothing, or items obstructing the face for the duration of measurement * Presence of facial tattoos, large birthmarks, or other skin alterations (scars, hemangiomas, vitiligo) on upper cheeks (cheekbone) or forehead of the subject * Condition that does not allow the subject to remain still for 60 seconds at a time * Subjects with cardiac arrhythmia * Any known medical condition which may result in an inaccurate measurement using the reference device * Subjects with the inability to complete an ECG.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Velocity Clinical Research

    Mobile, Alabama, 36608, United States

  • Velocity Clinical Research

    La Mesa, California, 91942, United States

  • Velocity Clinical Research

    Meridian, Idaho, 83642, United States

  • Velocity Clinical Research

    Cleveland, Ohio, 44122, United States

  • Velocity Clinical Research

    Columbia, South Carolina, 29204, United States

  • Velocity Clinical Research

    Cedar Park, Texas, 78613, United States

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