Cedars Sinai Medical Center Smidt Heart Institute
Los Angeles, California, 90048, United States
Location status: Recruiting
NCT Number: NCT07036926
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Los Angeles, California, 90048, United States
Location status: Recruiting
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
A novel, AI-generated, interactive peri-operative video education program. AI videos will be personalized using medical record chart data, specifically the patient's name, surgery date, and past medical history.
Time frame: From randomization to 30 days post-surgery
includes the following events: unplanned (i.e. patient initiated) phone calls, emails, clinic visits, and ED visits.
Contact information is provided by the study sponsor or research team.
Allen Armin Razavi, MD
CONTACT
Aminah Sallam, MD
CONTACT
Joanna Chikwe
Other
Video-Based AI-Generated Peri-operative Instructions for Mitral Valve Surgery: A Randomized Controlled Trial on Health Outcomes and Patient Experience
Acronym: VIP-IMPACT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06738992
Mitral Valve Repair Surgery
Guangzhou, Guangdong, China
View Trial DetailsNCT01694251
Mitral Valve Repair Surgery
Seoul, South Korea
View Trial Details