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AI avatar teaches heart patients how to heal – less pain, less worry?

NCT ID NCT07503678

Symptom relief Sponsor: Hasan Kalyoncu University Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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

Summary

This study tests whether a personalized AI-generated video, delivered by a nurse avatar, can improve recovery for people after coronary artery bypass surgery. About 128 patients will either get standard discharge instructions or the AI video plus standard care. Researchers will measure pain, anxiety, stress, and satisfaction to see if the high-tech approach helps patients feel better and recover faster.

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

About 128 people

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

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Feb 2027

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.

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: * Patients who have undergone coronary artery bypass graft (CABG) surgery. * Age 18 years or older. * Hemodynamically stable at the time of enrollment. * Able to understand and communicate in Turkish. * Able to use or have access to a mobile phone capable of viewing the educational video. * Able to provide informed consent. * Scheduled for routine postoperative follow-up at the study hospital. Exclusion Criteria: * Patients undergoing emergency CABG surgery. * Presence of severe cognitive impairment that prevents understanding or following instructions. * Diagnosed psychiatric disorders (e.g., schizophrenia, severe depression) that interfere with study participation. * Severe vision or hearing impairment that prevents receiving the education. * Presence of postoperative complications requiring intensive care readmission. * Patients with endocrine disorders affecting stress biomarkers (e.g., Cushing's syndrome, Addison's disease). * Chronic use of corticosteroids or medications that significantly alter cortisol levels. * Patients who decline to participate or withdraw consent. * Patients who are unable to complete follow-up assessments.

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Conditions

The condition(s) this trial relates to.

anxiety anxiety disorder coronary artery disorder Pain

As listed by the trial registrant

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

Anxiety Coronary artery disease Discharge education Nursing Pain Patient discharge Postoperative care Recovery of function Stress, physiological Surgical nursing

How to take part

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

  1. 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 ↗

  2. 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.

More trials for these conditions

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