Can wearables track stress in cardiologists during procedures?
NCT ID NCT07804927
First seen Sep 04, 2026 · Last updated Sep 04, 2026
Summary
This study tracks stress levels in interventional cardiology fellows and attending physicians using wearable devices and questionnaires. Researchers measure heart rate variability and self-reported stress before, during, and after procedures to see how stress changes with experience. The goal is to understand how these doctors cope with high-pressure work and recover afterward.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Wearable devices and stress assessments
- What this could lead to
- If it works, this could point toward ways to reduce stress and burnout among interventional cardiologists.
- What could go wrong
- The trial is small and observational, so results may not apply to all cardiologists. Wearable data may not fully capture stress.
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
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About 15 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2023
- Expected to finish
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Oct 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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 target study population is all interventional cardiology attendings and fellows at Minneapolis Heart Institute.
- Ages
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18 years and older
- Sex
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Anyone
Show the full entry requirements Hide 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: 1. Interventional Cardiology fellow or attending. 2. Age 18 years or older. 3. Willing and able to provide informed consent. 4. Access to smartphone (Apple or Android platform). 5. Willing and able to wear the wearable devices. Exclusion Criteria: 1- Any health condition that in the opinion of the investigator would preclude individual's participation in the study such as conditions that would preclude them from wearing the study wearables and participating to provide wearable data.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Minneapolis Heart Institute Foundation
RECRUITINGMinneapolis, Minnesota, 55407, United States
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