跳至主要内容
临床试验/NCT07187700
NCT07187700尚未招募不适用

Developing Trustworthy Artificial Intelligence (AI)-Driven Tools to Predict Vascular Disease Risk and Progression: the Prospective VASCUL-AID Study

Amsterdam UMC0 个研究点目标入组 1,100 人开始时间: 2025年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
1,100
主要终点
Development and internal validation of AI-driven tools to predict high or low risk disease progression in AAA and PAD.

研究概览

简要总结

Introduction:

Peripheral arterial disease (PAD) and abdominal aortic aneurysm (AAA) are vascular conditions associated with significant morbidity and mortality, with 25% of AAA patients and 23% of PAD patients being at a high risk of developing cardiovascular disease. Cardiovascular risk management can reduce the risk of major adverse cardiovascular events in AAA patients from 43% to 14%. However, cardiovascular risk is not always adequately addressed in these patients. The VASCUL-AID-PRO study aims to deliver clinically relevant prediction models using artificial intelligence and machine learning of patient outcomes to enable personalized management of vascular disease.

Method:

VASCUL-AID-PRO is a multi-centre international prospective cross-sectional study aiming to include 500 AAA patients and 600 PAD patients across 6 European centres. The aim is to achieve a follow-up time up to 4 years.

The study will include individuals aged 40-90 with either an abdominal aortic aneurysm (infrarenal, juxtarenal, pararenal, or suprarenal abdominal aortic aneurysm) or Fontaine stage 2 peripheral arterial disease.

The VASCUL-AID-PRO study will gather a variety of data from all participants, including clinical data, blood and tissue samples, cardiovascular lab values, imaging data, electrocardiograms, data from wearables and quality of life.

This data gathered will be used to further develop the multi model prediction models being developed on 5000 AAA and 6000 PAD patients included in the currently ongoing VASCUL-AID-RETRO study, with the aim of providing a clinically relevant prediction models of disease progression and other cardiovascular disease for AAA and PAD patients.

Furthermore, the models developed in the VASCUL-AID studies will be internally validated using a subset of patients from the VASCUL-AID-PRO study.

Ethical considerations:

Ethical and legal considerations are paramount throughout the VASCUL-AID project. To address these concerns, an ELSI framework will be developed and integrated into all stages of the project. This framework will be continuously updated to ensure alignment with evolving ethical, legal, and social standards. This framework will specifically focus on patient safety, data handling, AI regulation and implementation, and potential biases associated with AI.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
40 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Development and internal validation of AI-driven tools to predict high or low risk disease progression in AAA and PAD.

时间窗: From baseline to 4 years follow-up.

The VASCUL-AID AI tools aim to predict AAA (rupture, mortality, cerebrovascular accident) and PAD (mortality, myocardial infarction, major amputation) progression, MACE and MALE. The internal validation is done by comparing the predicted disease progression, MACE, MALE and mortality rates with actual disease progression.

次要结局

  • Accuracy of developed VASCUL-AID driven algorithms that classify AAA patients according to high or low risk disease progression.(From baseline to 4 years follow-up)
  • Patient reported outcome measures for AAA related quality of life.(From baseline to 4 year follow-up.)
  • Accuracy of developed VASCUL-AID driven algorithms that classify PAD patients according to high or low risk disease progression.(From baseline to 4 years follow-up)
  • Patient reported outcome measures for AAA and PAD.(From baseline to 4 years follow-up.)
  • Patient reported outcome measures for health-related quality of life.(From baseline to 4 years follow-up.)
  • Patient reported outcome measures for vascular quality of life for PAD.(From baseline to 4 year follow-up)
  • Questions regarding medical status.(From baseline to 4 year follow-up)
  • 6-minute walking test questionnaire(From baseline to 4 year follow-up)
  • Medication use questionnaire(From baseline to 4 year follow-up)
  • Smoking cessation questionnaire(From baseline to 4 year follow-up.)
  • Questionnaire regarding health-care provider communication.(From baseline to 4 year follow-up.)
  • Cost-effectiveness and Clinical Implementation Study(baseline to 4 years follow-up)

研究者

发起方
Amsterdam UMC
申办方类型
Other
责任方
Principal Investigator
主要研究者

Associate Prof. Dr. Kak Khee Yeung

Prof. Dr.

Amsterdam UMC

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