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Heart surgery patients may benefit from discharge videos

NCT ID NCT07528859

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
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 Results may not be published yet.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 This study
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This status has not been confirmed recently, so it may be out of date.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 tested whether adding a video to standard discharge education helps patients who have had coronary artery bypass graft (CABG) surgery feel more satisfied and less anxious. 120 patients were randomly assigned to receive either standard education, a standard video, or a personalized video. The study measured satisfaction and anxiety levels using questionnaires.

What this could mean

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

Active substance
video-assisted discharge education
What this could lead to
If it works, this could provide a simple, low-cost way to improve patient experience and reduce anxiety after heart surgery.
What could go wrong
The study was terminated early, so results may be incomplete. It is a small, single-center trial, so findings may not apply to all hospitals or patients.

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

120 people

The number who actually took part.

Started

Sep 2023

Finished

Feb 2024

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

A convenience sampling method was used. A total of 120 eligible patients who met the inclusion criteria and provided informed consent were enrolled in the study. Participants were randomly allocated into three parallel groups: standard video education, individualized video education, and control group.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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 and older * Patients who are in the discharge phase and eligible to receive discharge education * Able to read and understand Turkish * Able to communicate effectively * Willing to participate in the study and provide written informed consent Exclusion Criteria: * Diagnosis of severe psychiatric disorder * Presence of cognitive impairment or dementia * Visual or hearing impairment that would prevent participation in the education program * Development of major postoperative complications requiring intensive care * Patients who are not clinically stable at the time of discharge * Patients who withdraw from the study during the research process

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Conditions

The condition(s) this trial relates to.

coronary artery disorder Patient Satisfaction

As listed by the trial registrant

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

Coronary artery bypass graft surgery (CABG) Coronary artery disease (CAD) Postoperative discharge education

Contacts and locations

Locations

  • Gaziantep City Hospital, Dr. Ersin Arslan Training and Research Hospital

    Gaziantep, Gaziantep, 2700, Turkey (Türkiye)

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