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AI-based Frailty Assessment Tool for Patients Undergoing Cardiac Surgery

Frailty Assessment Tool for Patients Undergoing Cardiac Surgery Based on Artificial Intelligence Multimodal Non-contact Monitoring.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06096922
Enrollment
521
Registered
2023-10-24
Start date
2023-05-11
Completion date
2024-12-31
Last updated
2025-05-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Frailty

Keywords

Frailty, Cardiac surgery, Artificial intelligence, Non-contact monitoring

Brief summary

The main purpose of this study is to establish a frailty automatic evaluation index AI frailty index based on artificial intelligence multi-modal non-contact monitoring information analysis. At the same time, the study will explore the correlation between ' AI weakness index ' and perioperative and long-term prognosis and quality of life.

Detailed description

This is a prospective cohort study. Patients who undergoes elective cardiac surgery will be enrolled. We collect frailty scales, clinical information and multi-modal, non-contact monitoring information during hospitalization. One-year follow-up will be done. The non-contact monitoring information are used to predict the frailty scales to establish and validate an AI-based frailty assessment model AI frailty index. The AI frailty index will be further used to predict perioperative and long-term outcomes.

Interventions

OTHERNo intervention

No intervention

Sponsors

China National Center for Cardiovascular Diseases
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Elective cardiac surgery

Exclusion criteria

* Emergency surgery * Age ≤ 18 years * The clinical situation is unstable, such as frequent occurrence of coronary ischemia events, unstable heart failure, or acute events leading to severe discomfort symptoms or changes in vital signs * Unable to cooperate in completing research data collection due to severe neurological and psychiatric abnormalities or other reasons * Duration of postoperative ventilation \> 48 hours or inability to obtain scale data on the first day after surgery

Design outcomes

Primary

MeasureTime frameDescription
One-dimensional matrix vector composed of five frailty scale resultsBefore and after surgery, up to 2 weeksConsisting of five frailty scales: Edmonton frailty scale, FRAIL frailty scale, Fried frailty scale, Clinical frailty scale, and SPPB

Secondary

MeasureTime frameDescription
1-year adverse events1 year post operativeIncluding death, readmission, stroke, myocardial infarction, renal insufficiency or renal failure, dialysis, atrial fibrillation, peripheral vascular embolism, bleeding events, heart failure
EQ-5D score1 year post operativeThe score of EQ-5D questionnaire
QOR-15 score1 year post operativeThe score of QOR-15 questionnaire
Edmonton frailty scale score1 year post operativeThe Edmonton frailty scale consists of 11 items for a composite score of 0 to 17, and higher scores mean a worse outcome.
FRAIL frailty scale score1 year post operativeThe FRAIL frailty scale consists of 5 items, with 3 of 5 required to diagnose frailty.
30-day adverse events30 days post operativeIncluding death, readmission, stroke, myocardial infarction, renal insufficiency or renal failure, dialysis, atrial fibrillation, peripheral vascular embolism, bleeding events, heart failure
Clinical frailty scale score1 year post operativeThe Clinical frailty scale is scored 1 to 9 based on a semiquantitative evaluation of the patient's symptoms, mobility, inactivity, exhaustion, and disability for basic activities of daily living and instrumental activities of daily living, and higher scores mean a worse outcome.
Short Physical Performance Battery scale score1 year post operativeThe Short Physical Performance Battery scale consists of 3 physical tests, with each scored 0 to 4 for a composite score of 0 to 12, and higher scores mean a better outcome.
Perioperative adverse eventsFrom surgery to discharge, up to 7 daysIncluding all cause death, stroke, renal insufficiency, deep sternal wound infection, and reoperation
Area under receiver operating curve (AUC)At the end of follow-up (1 mouth)Area under receiver operating curve of algorithm in predicting frailty scales and outcomes
Fried frailty scale score1 year post operativeThe Fried frailty scale consists of 5 items, with 3 of 5 required to diagnose frailty.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026