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Can your smartwatch replace hospital monitors before surgery?

NCT ID NCT07322523

Knowledge-focused Sponsor: Halil Kalaycı Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 checks if Samsung smartwatches can accurately measure blood pressure, heart rate, oxygen levels, anxiety, and sleep quality in 60 patients waiting for disc herniation surgery. Researchers compare smartwatch readings to standard medical devices and questionnaires. The goal is to see if wearable tech can reliably track patients before surgery, potentially making monitoring easier and less intrusive.

What this could mean

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

Active substance
Samsung smartwatch
What this could lead to
If successful, this could show that smartwatches are a reliable tool for monitoring patients before surgery, potentially improving care without extra equipment.
What could go wrong
This is a small, early-stage study (60 participants) focused on accuracy, not on improving health outcomes. The smartwatch may not match medical-grade devices, and results may not apply to other surgeries or settings.

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 60 people

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

Started

Nov 2025

Expected to finish

Mar 2026

An estimate. End dates often move.

Lead sponsor

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 study population comprises adult inpatients admitted to the Neurosurgical Ward of the university hospital due to intervertebral disc herniation for preoperative assessment and monitoring.

Ages

22 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * 22 years and older * Currently receiving preoperative care/assessment for disc herniation surgery. * No history of any cardiovascular disease other than controlled hypertension. * Willingness to wear the smartwatch for a minimum of 8 consecutive hours during the night before surgery. * Ability to follow all instructions related to the smartwatch operation and data collection independently. * No known allergy to nickel. Exclusion Criteria: * Patients who are currently receiving prescribed medication specifically for sleep in the clinical setting. * Refusal or unwillingness to participate in the study. * The participant fails to wear the smartwatch correctly or appropriately as per study instructions, leading to incomplete or unreliable data collection.

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Conditions

The condition(s) this trial relates to.

anxiety disorder insomnia Intervertebral Disc Displacement lumbar disk herniation, susceptibility to

As listed by the trial registrant

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

Cervical disc herniation Disc herniation, lumbar Disc herniations Preoperative anxiety score Preoperative care Sleep quality Smart watch Surgical nursing Vital signs monitoring Wearable devices

How to take part

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

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Erciyes University

    RECRUITING

    Kayseri, Turkey (Türkiye)

More trials for these conditions

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