Smartwatches track dentist stress during root canals
NCT ID NCT07498348
First seen Jun 27, 2026 · Last updated Jul 10, 2026 · Updated 1 time
Summary
This study will have about 12 endodontists (dental specialists) wear an Apple Watch during routine root canal procedures to track their heart rate changes. A researcher will note the different stages of treatment to see which parts are most stressful. The goal is to better understand occupational stress in dentistry, not to test any treatment.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 12 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 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
A total of approximately 132 subjects will be enrolled in this study, consisting of approximately 12 endodontics (primary subjects) and approximately 120 patients (secondary subjects). Each participating endodontics will be observed during approximately 10 endodontic treatment sessions, resulting in an estimated total of 120 clinical sessions for data collection. Each patient will participate in one clinical encounter only, while resident participation will continue throughout the data collection period.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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 for Primary Subjects (endodontics residents) : * Active enrollment in an accredited endodontics residency program during the data-collection period * Routine clinical involvement in primary root canal treatment and/or retreatment * Willingness to wear a wrist-worn heart rate monitoring device during clinical sessions * Willingness to complete the Perceived Stress Questionnaire (PSQ) at baseline and at the conclusion of participation * Absence of medical or dermatologic conditions that would preclude safe or accurate wrist-worn heart rate monitoring Inclusion Criteria for secondary Subjects (Patients): * Scheduled to receive standard endodontic care with a participating endodontics resident during the study period * Willingness to allow the presence of a non-intervening observer * Willingness to allow collection of minimal, approved visit-level variables * Adult patients able to provide written informed consent * Minor patients (under 18 years of age) with parent or legally authorized representative permission * Assent obtained from minors as follows: * Verbal assent for minors aged 7-12 years * Written assent for minors aged 13-17 years * No formal assent required for children under 7 years of age (developmentally appropriate explanation provided when feasible) * Ability of patient or legally authorized representative to understand and communicate in English Exclusion Criteria for Primary Subjects (endodontics residents) : * Not engaged in clinical endodontic care during the study window * Known dermatologic, cardiovascular, neurologic, or other medical conditions that could interfere with safe or accurate heart rate monitoring * Unwilling or unable to provide informed consent or comply with study procedures Exclusion Criteria for secondary Subjects (Patients): * Decline consent, permission, or assent * Withdraw participation at any time * Prisoners or individuals under custodial supervision * Pregnant patients
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
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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University of Illinois Chicago (UIC) College of Dentistry
Chicago, Illinois, 60612, United States
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Other studies related to the condition(s) this trial covers.
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