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临床试验/NCT07839845
NCT07839845已完成不适用

A Retrospective Observational Substudy of LDL Cholesterol Changes and Treatment-Target Attainment in the AIDAVA G1 Post-Myocardial Infarction Cohort

North Estonia Medical Centre1 个研究点 分布在 1 个国家目标入组 37 人开始时间: 2024年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
37
试验地点
1
主要终点
Percentage of participants with LDL-C below 1.4 mmol/L at follow-up.

研究概览

简要总结

This retrospective substudy describes low-density lipoprotein cholesterol (LDL-C) changes and treatment-target attainment among patients with previous myocardial infarction who participated in the AIDAVA first-generation (G1) prototype evaluation in Estonia, Austria and the Netherlands. Existing study data and clinical records are analysed. The LDL-C research question was developed after the original evaluation was planned and was not its prespecified efficacy endpoint. No additional intervention, treatment assignment, visit or blood sampling is introduced by this substudy. Findings are exploratory and cannot establish a causal effect of AIDAVA participation.

详细描述

AIDAVA developed an AI-assisted system for integrating, curating and reusing personal health data. The original evaluation addressed technical performance, usability and acceptance. Cardiovascular participants contributed existing clinical records and longitudinal data, including home blood-pressure measurements, with support from study nurses and data curators. The cardiovascular protocol also envisaged automatic SMART risk-score assessment.

This registration covers only the secondary LDL-C analysis of the G1 post-myocardial infarction cohort. It does not register the full AIDAVA project, breast-cancer evaluation or G2 prototype evaluation. The original evaluation was not registered. This summary was prepared after the LDL-C analysis and does not represent prospective specification of its hypotheses, outcomes or analysis methods.

研究设计

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

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Participation in the AIDAVA G1 cardiovascular cohort
  • •Available baseline and follow-up LDL-C measurements with ascertainable measurement dates.

排除标准

  • •Absence of the required paired baseline and follow-up LDL-C measurements
  • •Missing patient consent

研究组 & 干预措施

AIDAVA G1 post-myocardial infarction cohort.

Previous participation in two-week G1 health-data curation and prototype testing with nurse/curator guidance, and home blood-pressure data collection. These activities occurred in the original evaluation; no exposure is assigned in this retrospective substudy.

结局指标

主要结局

Percentage of participants with LDL-C below 1.4 mmol/L at follow-up.

时间窗: Day 365

Percentage of participants with LDL-C below 1.8 mmol/L at follow-up.

时间窗: Day 365

次要结局

未报告次要终点

研究者

发起方
North Estonia Medical Centre
申办方类型
Other
责任方
Sponsor

研究点 (1)

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