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AI listens in to free up Doctors' time

NCT ID NCT07647159

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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This study tested an AI voice assistant that listens to conversations between neurologists and patients, then automatically fills out electronic medical records. Researchers timed 320 visits with and without the AI to see if it saved doctors time and improved patient care. The goal is to reduce paperwork so doctors can spend more time with patients.

What this could mean

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

Active substance
AI-based voice assistant software
What this could lead to
If successful, this could reduce paperwork for neurologists, giving them more time to focus on patients during visits.
What could go wrong
This is a small pilot study with only 5 doctors in Moscow. The AI may not work as well in other languages or settings, and it might not save time in real-world use.

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

320 people

The number who actually took part.

Started

Oct 2025

Finished

Jan 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 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: 1. First-time outpatient neurology visit conducted by a participating physician according to the approved consultation script. 2. Age 18 years or older. 3. Signed informed consent to participate in the study. 4. Signed consent to processing of personal data. 5. Clinical condition that allowed the patient to complete the modified Patient Satisfaction Questionnaire 8 (PSQ-8). Exclusion Criteria: 1. Consultation longer than 45 minutes. 2. Consultation shorter than 5 minutes, not requiring a full examination (e.g., prescription renewal, clarification of follow-up questions only). 3. Technical failures preventing valid interpretation of the consultation or its timing (microphone failure, malfunction of the recording software, malfunction of the Service). 4. Deviation from the approved consultation script.

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Conditions

The condition(s) this trial relates to.

Burnout, Professional ichthyosis occupation-related stress disorder Patient Satisfaction

As listed by the trial registrant

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

Contacts and locations

Locations

  • Research and Practical Clinical Center for Diagnostics and Telemedicine Technologies of the Moscow Health Care Department

    Moscow, 125051, Russia

More trials for these conditions

Other studies related to the condition(s) this trial covers.