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Chatting about AI before surgery may calm nerves, study finds

NCT ID NCT07393945

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested whether a short, clear conversation about how artificial intelligence is used in surgery care can reduce anxiety and improve a patient's sense of control before an operation. 120 adults scheduled for elective surgery were randomly assigned to either receive this structured AI talk or a general supportive chat from a nurse. The goal was to see if addressing AI-related uncertainty helps patients feel more prepared and less worried.

What this could mean

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

Active substance
structured communication about artificial intelligence
What this could lead to
If it works, this could provide a simple, non-drug way to help patients feel less anxious and more in control before surgery.
What could go wrong
This is a small, completed study with 120 participants, so results may not apply to everyone. It only measures feelings, not actual health outcomes.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

120 people

The number who actually took part.

Started

Feb 2026

Finished

Apr 2026

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.

Ages

18 to 65 years

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: * Adults aged 18 to 65 years. * Scheduled for elective surgical procedures. * Able to communicate in Turkish. * At least primary school literacy. * Able and willing to provide written informed consent. * Able to complete self-report questionnaires before surgery. Exclusion Criteria: * Emergency surgical procedures. * Known diagnosis of psychiatric disorder. * Current use of anxiolytic or antidepressant medications. * Cognitive impairment or communication barriers that may interfere with study participation. * American Society of Anesthesiologists (ASA) physical status classification of IV or higher. * Severe visual or hearing impairment that prevents participation in the communication session or completion of questionnaires. * Previous participation in this study.

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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

  • Ağrı Training and Research Hospital

    Ağrı, Merkez, Turkey (Türkiye)

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