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CardiacNCT07400172

AI-Generated Video Feedback to Improve Technical Skills in Coronary Artery Bypass Grafting

A study testing AI-Guided Video Feedback Intervention in people with Cardiac and Surgery (Cardiac), run by China National Center for Cardiovascular Diseases at 1 site in China.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

This study aims to evaluate whether targeted video feedback generated by an artificial intelligence (AI)-based surgical performance assessment model can support improvement in technical skills among cardiac surgeons performing coronary artery bypass grafting (CABG). Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Cardiac, Surgery (Cardiac), Education
What is being tested?
AI-Guided Video Feedback Intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteChina
Study dates
31 Jan 2026to 30 Apr 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Baseline AI-assessed technical performance ranked in the lower 50% within the scoring system in CAMERA study (NCT06739005)

Who cannot join

  • Unwilling to attend

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Lihua Zhang Zhang, M.D, Ph.D contact

13810483387

zhanghaibo@fuwai.com

China1 site
  • Fuwai Hospital

    Beijing, Beijing Municipality, 102300

    Lihua Zhang Zhang, M.D, Ph.D, 15920826832, leilubi@fuwai.com

Other trials in China

About this study

This study aims to evaluate whether targeted video feedback generated by an artificial intelligence (AI)-based surgical performance assessment model can support improvement in technical skills among cardiac surgeons performing coronary artery bypass grafting (CABG). This is a single-group, self-controlled, pre-post interventional study. Participating surgeons will submit a baseline CABG surgical video, which will be assessed by both an AI model and blinded human expert raters using standardized scoring criteria. Based on the AI assessment, surgeons will receive personalized video feedback highlighting operative steps associated with lower technical performance. After a one-month self-directed review period, a follow-up CABG surgical video will be submitted and evaluated using the same process. Changes in human-rated technical skill scores between baseline and follow-up will be used to assess the potential educational impact of AI-generated video feedback.

Read the detailed description

Coronary artery bypass grafting (CABG) is a complex surgical procedure that requires a high level of technical skill from cardiac surgeons. Variability in surgical technique may influence procedural quality and patient outcomes. Recent advances in artificial intelligence (AI) have enabled automated assessment of surgical performance using operative video data, creating new opportunities for objective feedback and surgical education.

This study aims to evaluate whether targeted video feedback generated by an AI-based surgical performance assessment model can help cardiac surgeons improve their technical skills in CABG procedures. Participating surgeons whose baseline technical performance ranked in the lower half of the AI scoring system will receive personalized video feedback highlighting operative steps and maneuvers associated with lower performance scores.

In this single-group, self-controlled study, each participating surgeon will submit a baseline CABG surgical video, which will be independently evaluated by both the AI model and a panel of experienced cardiac surgeons using standardized scoring criteria. After receiving AI-generated video feedback, surgeons will be given one month to review and reflect on the feedback without additional formal training or coaching. A follow-up CABG surgical video will then be submitted and assessed using the same evaluation process.

The primary outcome of the study is the change in technical skill scores assigned by human expert raters between the baseline and follow-up videos. Secondary outcomes include surgeons' self-assessments of AI-identified performance deficits, agreement between AI-generated feedback and human expert feedback, and selected patient postoperative in-hospital outcomes. The findings of this study may inform the role of AI-assisted video feedback as a scalable educational tool for surgical skill development.

Being tested
AI-Guided Video Feedback Intervention
Keywords
Coronary Artery Bypass Grafting, Surgical Education, Video-Based Feedback, Artificial Intelligence

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • AI-Guided Video Feedback InterventionBehavioural

    Participants in this study will receive a personalized educational intervention consisting of AI-generated video feedback based on their baseline coronary artery bypass grafting (CABG) surgical videos. The AI model analyzes surgical performance and identifies specific operative steps with lower technical skill scores. Curated video clips highlighting these areas are provided to the surgeons for self-review and reflection. No additional formal training or coaching is given during the one-month intervention period, after which a follow-up surgical video is submitted for re-evaluation.

Study groups in NCT07400172
Study groupRoleWhat they receive
AI-Guided Video Feedback InterventionExperimentalParticipants in this study will receive a personalized educational intervention consisting of AI-generated video feedback based on their baseline coronary artery bypass grafting (CABG) surgical videos. The AI model analyzes surgical performance and identifies specific operative steps with lower technical skill scores. Curated video clips highlighting these areas are provided to the surgeons for self-review and reflection. No additional formal training or coaching is given during the one-month intervention period, after which a follow-up surgical video is submitted for re-evaluation.
Receives: Behavioral: AI-Guided Video Feedback Intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Human Expert-Rated Technical Skill Score Between Baseline and Follow-Up CABG Videos

    The primary outcome is the change in technical skill scores assigned by a panel of blinded human expert raters, who independently evaluate anonymized coronary artery bypass grafting (CABG) surgical videos submitted at baseline and one month after receiving AI-generated video feedback. The scoring uses a standardized rubric to assess overall surgical technical performance. The higher score, the better performance: respect for tissue, time and motion, instrument handling, knowledge of instruments, use of assistants, flow of operation and forward planning, and knowledge of the specific procedure. Each domain was scored on a 5-point Likert scale, where 1 indicated poor performance and 5 represented excellence. In addition, each rater provided an overall impression score (1-5) to capture their holistic assessment of surgical performance. The two scores were scaled to 100 points and the final score consists of 70% of 7-domain rating sum scores and 30% of overall impression score.

    Measured: Baseline, 1 month

Secondary outcomes (13)
  1. Surgeon self-assessments of the AI feedback

    Surgeons will review the AI-generated video clips highlighting technical performance deficits and complete a self-assessment questionnaire evaluating their satisfaction of the AI feedback.

    Measured: 1 month

  2. Consistency between AI feedback and human expert feedback.

    This outcome assesses the consistency between the AI-generated surgical performance feedback and evaluations provided by human expert raters. AI-score was generated by a two-stage deep learning framework and human expert raters' score was generated by a validated 7-domain rating scale as detailed in the primary outcome. The intraclass correlation coefficient (ICC) will be used to assess the consistency between the surgical technique scores assessed by the AI model and those rated by human expert raters.

    Measured: Baseline, 1 month

  3. Postoperative in-hospital outcomes: the icidence of major complications

    Patient postoperative in-hospital outcomes will be collected and analyzed to explore any associations with changes in surgeon technical performance following the AI feedback intervention. The incidence of major complications (a composite outcome of death, acute kidney injury, myocardial infarction and stroke)

    Measured: Baseline, 1 month

  4. Postoperative in-hospital outcomes: the incidence of death

    The associations with changes in surgeon technical performance following the AI feedback intervention and the incidence of death.

    Measured: Baseline, 1 month

  5. Postoperative in-hospital outcomes: the incidence of acute kidney injury

    The associations with changes in surgeon technical performance following the AI feedback intervention and the incidence of acute kidney injury.

    Measured: Baseline, 1 month

  6. Postoperative in-hospital outcomes: the incidence of myocardial infarction

    The associations with changes in surgeon technical performance following the AI feedback intervention and the incidence of myocardial infarction.

    Measured: Baseline, 1 month

  7. Postoperative in-hospital outcomes: the incidence of stroke

    The associations with changes in surgeon technical performance following the AI feedback intervention and the incidence of stroke.

    Measured: Baseline, 1 month

  8. Postoperative in-hospital outcomes: the incidence of secondary thoracotomy

    The associations with changes in surgeon technical performance following the AI feedback intervention and the incidence of secondary thoracotomy.

    Measured: Baseline, 1 month

  9. Postoperative in-hospital outcomes: the incidence of IABP implantation

    The associations with changes in surgeon technical performance following the AI feedback intervention and the incidence of IABP implantation.

    Measured: Baseline, 1 month

  10. Postoperative in-hospital outcomes: the incidence of ECMO implantation

    The associations with changes in surgeon technical performance following the AI feedback intervention and the incidence of ECMO implantation.

    Measured: Baseline, 1 month

  11. Postoperative in-hospital outcomes: the incidence of bedside hemofiltration

    The associations with changes in surgeon technical performance following the AI feedback intervention and the incidence of bedside hemofiltration.

    Measured: Baseline, 1 month

  12. Postoperative in-hospital outcomes: the incidence of peritoneal dialysis

    The associations with changes in surgeon technical performance following the AI feedback intervention and the incidence of peritoneal dialysis.

    Measured: Baseline, 1 month

  13. Postoperative in-hospital outcomes: the incidence of tracheotomy

    The associations with changes in surgeon technical performance following the AI feedback intervention and the incidence of tracheotomy.

    Measured: Baseline, 1 month

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Feb 2026
  2. Study start31 Jan 2026 (estimated)
  3. Primary completion31 Mar 2026 (estimated)
  4. Study completion30 Apr 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Model description
This study uses a single-group, self-controlled interventional model. Each participating cardiac surgeon acts as their own control by comparing technical skill performance before and after receiving an AI-generated targeted video feedback intervention. The intervention consists of personalized surgical video clips highlighting suboptimal technical maneuvers identified by an AI-based assessment model. No randomization or control group is involved. The study evaluates changes in surgical skill scores assessed by blinded human experts pre- and post-intervention to determine the potential educational impact of the AI feedback.
Masking
None (open label)
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07400172
Sponsor's protocol ID
FW-HSS
Status last verified
Feb 2026
First submitted
23 Dec 2025
Last updated
10 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Data collected for the study will be made available publicly upon reasonable request (huss@fuwai.com) after two years of publication.

Questions about this trial

What is this clinical trial studying?

A study testing AI-Guided Video Feedback Intervention in people with Cardiac and Surgery (Cardiac), run by China National Center for Cardiovascular Diseases at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 10 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Lihua Zhang Zhang, M.D, Ph.D (13810483387, zhanghaibo@fuwai.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Human Expert-Rated Technical Skill Score Between Baseline and Follow-Up CABG Videos (time frame: Baseline, 1 month). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Feb 2026.

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