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Whole-process Quality Improvement of Endovascular Treatment Basd on an AI-aided Clinical Feedback System

Not Applicable
Recruiting
Conditions
Stroke, Acute
Interventions
Behavioral: AI-aided clinical feedback system coupled with multi-aspect intervention basd on Behaviour Change Wheel model
Registration Number
NCT05874596
Lead Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
Brief Summary

A clustered randomized control trial to evaluate whether multi-aspect intervention based on an AI-aided clinical feedback system could improve the quality of EVT and functional outcome of patients.

Detailed Description

Endovascular treatment (EVT) is the standard treatment for acute ischemic stroke (AIS) caused by large vessel occlusion (LVO) according to current guidelines. However, while a rapidly-growing number of stroke centers become capable of performing EVT, the general quality of EVT remains unsatisfied, resulting in a considerable proportion of patients who could not reach functional independence. Our pre-established artificial intelligence (AI)-aided clinical feedback system could dynamically record and report key timepoints of EVT in-hospital process. Combined with multi-aspect intervention via remote/on-site surveillance and education, this may be a potential solution for quality improvement of EVT. Therefore, the aim of the study is to evaluate whether an AI-aided clinical feedback system coupled with multi-aspect intervention could improve the quality of EVT. Twenty hospitals with annual EVT cases \> 30 will be 1:1 randomized into intervention group and control group. The intervention group will receive AI-based clinical feedback system coupled with multi-aspect intervention, including remote/on-site surveillance and education regarding in-hospital workflow and surgical procedures of EVT. The control group only deploys AI-aided clinical feedback system. The primary outcome is the ratio of good functional outcome (mRS \> 2) at 3 month.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
1221
Inclusion Criteria
  • Age > 18
  • AIS patients receiving EVT within 24 hours of stroke onset
  • Written informed consent is obtained
Exclusion Criteria
  • Patients refuse to participate in this study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionAI-aided clinical feedback system coupled with multi-aspect intervention basd on Behaviour Change Wheel modelAI-aided clinical feedback system coupled with multi-aspect intervention based on the Behaviour Change Wheel model
Primary Outcome Measures
NameTimeMethod
Ratio of favorable functional outcome at 3 month3 months

Ratio of patients with mRS \> 2 at 3-month follow up

Secondary Outcome Measures
NameTimeMethod
Ratio of hemorrhagic transformation at 24 hour24 hours

Ratio of hemorrhagic transformation at 24 hour after EVT

Door to groin puncture time24 hours

Time interval between admission and groin puncture

Ratio of door to groin puncture time < 90 min24 hours

Time interval between admission and groin puncture \<90 min

mRS score at 3 month3 months

mRS score at 3-month follow up

Ratio of successful reperfusion24 hours

Ratio of patients achieving modified thrombolysis in cerebral infarction (mTICI) 2b or 3

Ratio of good functional outcome at 3 month3 months

Ratio of patients with mRS \> 1 at 3-month follow up

Mortality at 3 month3 months

Mortality at 3-month follow up

Ratio of symptomatic intracranial hemorrhage at 24 hour24 hours

Ratio of symptomatic intracranial hemorrhage at 24 hour after EVT

Ratio of door to groin puncture time < 60 min24 hours

Time interval between admission and groin puncture \<60 min

Procedural duration24 hours

Time interval between groin puncture and last time of digital subtraction angiography

Trial Locations

Locations (1)

Second Affiliated Hospital, School of Medicine, Zhejiang University

🇨🇳

Hangzhou, China

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