跳至主要内容
临床试验/NCT06600620
NCT06600620暂停不适用

Intelligent Monitoring to Predict Atrial Fibrillation [NOTE-AF]: Clinical Study 1 for the "Health Virtual Twins for the Personalised Management of Stroke Related to Atrial Fibrillation (TARGET)" Project

Liverpool University Hospitals NHS Foundation Trust2 个研究点 分布在 1 个国家目标入组 1,200 人开始时间: 2024年9月23日最近更新:
适应症

试验速览

阶段
不适用
状态
暂停
入组人数
1,200
试验地点
2
主要终点
To determine the incidence of clinical and subclinical episodes of AF in acutely unwell patients and to generate data for the development and validation of virtual twins and clinical decision support tools.

研究概览

简要总结

Atrial Fibrillation (AF) is the commonest arrhythmia worldwide, affects 5% of people over the age of 65 and increases the risk of stroke and heart failure. The investigators aim to detect clinical and subclinical episodes of atrial fibrillation lasting >30 seconds to develop risk prediction models to identify patients at high risk for ischaemic stroke.

详细描述

Atrial Fibrillation (AF) is the commonest arrhythmia worldwide, affects 5% of people over the age of 65 and increases the risk of stroke and heart failure. Among acutely unwell patients; arrhythmias and myocardial injury are common and associated with increased mortality, morbidity, and healthcare costs. Cardiovascular comorbidities in these high-risk patients include hypertension (47%), dyslipidaemia (29%) and ischaemic heart disease (11%).

The investigators aim to detect clinical and subclinical episodes of atrial fibrillation lasting 30 seconds to develop risk prediction models to identify patients at high risk for ischaemic stroke. Data will serve to develop and validate bedside clinical decision support tools and digital twins. Patients who develop episodes of AF as part of acute illness, will suffer further episodes of AF within one year in over 20% of cases with 27% progressing to paroxysmal/permanent AF. The true incidence of AF is unknown in acutely unwell patients as a significant percentage of AF episodes remain undetected with conventional intermittent monitoring. Patients experiencing short self-terminating episodes of AF carry a 5-fold risk of developing continuous AF and double the risk of stroke and thromboembolic events. Patients suffering episodes of AF often remain asymptomatic but are at increased risk of heart failure and death at one year. Compared to routine intermittent manual measurement of vital signs, wireless continuous vital sign monitoring systems (wCVSM) detect deviations instantaneously with the option of alerting clinical staff in real time via mobile phone applications. Accurate categorization of alerts into false and true events is essential for developing intelligent software that can be embedded into monitoring systems. Continuous ECG and vital signs monitoring can detect AF episodes more reliable, trigger timely investigations and support longer term treatment plans.

Changes in patient pathways and introduction of novel devices to alert healthcare staff on the potential of clinical events require buy-in from all stakeholders. It is therefore essential to evaluate user acceptance and to determine perceptions of users before rolling out a novel patient pathways or implementation of a new device within an organization. The investigators therefore wish to explore users' views of the device, wearing the device and potential areas for improvement using questionnaires for patients and health care staff and by conducting semi-structured interviews with healthcare staff.

Primary objective To determine the true cardiovascular event rate (defined as at least one of the following criteria: episodes of AF, New Regional Wall Motion Abnormalities, raised cardiac biomarkers hs-troponin T and NT-pro-BNP) versus false cardiovascular events detected by continuous wireless remote monitoring.

Secondary objective To determine patient acceptability and usability for health care professionals of a novel remote monitoring device with automated alert function.

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
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients ≥50 years
  • Estimated risk of developing new episodes of AF greater than 5%
  • Sinus rhythm at presentation
  • One of the following acute conditions:
  • Patients admitted or referred to Critical Care (NOTE-AF ICU)
  • Patients admitted to hospital with acute heart failure (NOTE-AF HF)
  • Patients admitted to Emergency Services with sepsis or infection (NOTE-AF Sepsis)
  • Patients post upper gastrointestinal surgery (NOTE-AF PULSE-GI)
  • Patients post vascular interventions (NOTE-AF Vasc)
  • Patients with acute respiratory failure (NOTE-AF Resp)
  • Patients admitted after acute stroke (NOTE-AF stroke)

排除标准

  • Atrial fibrillation or atrial flutter at the time of screening
  • Patients in atrial fibrillation or atrial flutter at time of preoperative assessment or admission to hospital
  • Paced cardiac rhythm
  • Inability to obtain consent
  • Allergy to plaster or silicone
  • Expected hospital stay less than 48 hours

结局指标

主要结局

To determine the incidence of clinical and subclinical episodes of AF in acutely unwell patients and to generate data for the development and validation of virtual twins and clinical decision support tools.

时间窗: 48 months

Number of episodes of AF and duration of each AF episode

次要结局

  • Length of hospital stay(48 months)
  • Hospital readmissions within 90 days(48 months)
  • Recurrence of AF episodes(48 months)
  • Hospital and 90-day Mortality(48 months)
  • Time spent in AF(48 months)
  • Number of AF episodes(48 months)
  • Complications of AF(48 months)
  • High sensitivity Troponin concentrations in patients with AF episodes(48 months)
  • Echocardiographic changes in patients with AF episodes(48 months)
  • mHealth App Usability Questionnaire(48 months)
  • Percentage change of troponin concentrations in patients with and without episodes of AF(48 months)
  • Time wireless continuous vital signs monitoring device is attached(48 months)
  • Number of cardiovascular alerts(48 months)
  • Number of non-cardiovascular alerts(48 months)
  • Number of alerts reflecting clinical changes(48 months)
  • Number of alerts reflecting artefacts or non-clinical events(48 months)
  • Change in inflammatory markers white cell count, C-reactive protein and procalcitonin over time(48 months)
  • RWMA score, atrial size and volume, left ventricular strain rate, standard echocardiographic measurements as per british society of echocardiography recommendations(48 months)

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (2)

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