Video-Based AI-Generated Peri-operative Instructions for Mitral Valve Surgery

Last updated: February 23, 2026
Sponsor: Joanna Chikwe
Overall Status: Active - Recruiting

Phase

N/A

Condition

Cardiac Surgery

Treatment

Artificial Intelligence Video Education Arm

Clinical Study ID

NCT07036926
STUDY00003876
  • Ages > 18
  • All Genders

Study Summary

  1. The purpose of this study is to evaluate the impact of a novel, AI-generated, interactive peri-operative video education program on total unplanned healthcare utilization

  2. The main procedures are questionnaires and watching a video.

  3. The subject population includes patients who are scheduled for isolated mitral valve repair surgery.

  4. All study procedures will occur here at Cedars Sinai.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Adult patients ≥ 18 years planned for elective, isolated MV repair.

  2. Provide Informed consent

Exclusion

Exclusion Criteria:

  1. Insufficient computer/smart device knowledge. Children or caregivers can assist, butpatients should be able to access their own email or text messages and navigate tothe internet to use the provided AI generated educational intervention.

  2. Inconsistent access to a smart device with internet connection throughout the studyperiod.

  3. Inability to speak, read, and understand English or Spanish

  4. Need for any concomitant procedure at the time of MV repair

Study Design

Total Participants: 100
Treatment Group(s): 1
Primary Treatment: Artificial Intelligence Video Education Arm
Phase:
Study Start date:
August 01, 2025
Estimated Completion Date:
December 31, 2026

Study Description

This study is a prospective, single center, randomized trial comparing an AI-generated peri-operative video education program to standard of care education (1:1 ratio) in patients undergoing MV repair. The trial will be conducted in Southern California. The primary aim of this study is to evaluate the impact of a novel, AI-generated, interactive peri-operative video education program on total unplanned healthcare utilization, defined as a composite of hospital readmissions, ED visits, and unplanned outpatient visits, among patients undergoing mitral valve (MV) repair compared with standard of care education. The secondary aim is to analyze the association between utilization of this educational program with hospital length of stay (LOS) and patient cardiovascular medication compliance compared to standard of care education. The tertiary aim of this trial is to evaluate a range of patient-centered outcomes (levels of anxiety, satisfaction, and discharge location) following receipt of this educational program compared with standard of care.

Connect with a study center

  • Cedars Sinai Medical Center Smidt Heart Institute

    Los Angeles 5368361, California 5332921 90048
    United States

    Active - Recruiting

Map preview placeholder

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.