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Wrist wearables could replace chest patches for heart monitoring

NCT ID NCT07684807

Knowledge-focused Sponsor: Corsano Health B.V. Source: ClinicalTrials.gov ↗

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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 06, 2026 · Last updated Jul 07, 2026 · Updated 1 time

Summary

This study collects data from 50 healthy adults who wear both a wrist device and a chest ECG patch for 24 hours. The goal is to train artificial intelligence to reconstruct detailed heart signals—especially the QT interval—from the wrist's light-based pulse readings. If the AI works, it could allow continuous heart monitoring from a simple wristband.

What this could mean

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

What this could lead to
If successful, this could enable continuous heart monitoring from a wrist-worn device without needing a chest patch, making it easier to detect heart rhythm problems.
What could go wrong
This is a small, early-stage data collection study. The AI may not work well enough for clinical use, and results from healthy volunteers may not apply to people with heart conditions.

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

About 50 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jul 2026

An estimate. Start dates often move.

Expected to finish

Oct 2026

An estimate. End dates often move.

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

Healthy adult volunteers, including hospital employees, recruited at a single clinical site.

Ages

18 years and older

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: * Able to provide written informed consent. * Willing and able to comply with all study procedures and attend the required study visits. * Age ≥18 years. * Able to read or understand Dutch or English. Exclusion Criteria: * Children/minors or vulnerable individuals. * Skin conditions or allergies preventing safe wear of the CardioWatch or ECG electrodes. * Any condition that, in the investigator's opinion, may interfere with study completion or data quality. * Compromised circulation, injury, or physical malformation at sensor sites. * Known clotting disorders or current prescription anticoagulant therapy. * Other health conditions preventing safe participation. * Wrist circumference \<14 cm or \>23 cm. * Any participant who, in the investigator's opinion, does not meet study requirements

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As listed by the trial registrant

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

Electrocardiography (ECG) Healthy volunteers Photoplethysmography

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  2. A doctor treating you

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