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临床试验/NCT05653726
NCT05653726Unknown不适用

Impact of Noninvasive Telemonitoring on Clinical Events, Healthcare Resource Use and Costs in Heart Failure

Hospital Universitario 12 de Octubre1 个研究点 分布在 1 个国家目标入组 390 人开始时间: 2023年11月29日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
390
试验地点
1
主要终点
Health care costs

研究概览

简要总结

The goal of this clinical trial is to know if telemonitoring and telematic follow-up reduces the healthcare resources utilization, healthcare costs and non-healthcare costs of patients with high-risk heart failure. The main questions it aims to answer are:

  • Does telematic follow-up reduce de use of healthcare resource utilization of patients with heart failure?
  • Is telematic follow-up cost-efficient in terms of reducing direct healthcare costs in heart failure patients?
  • Is telematic follow-up cost-efficient in terms of reducing non-healthcare costs in heart failure patients? Participants will be randomized to usual care (control group) or telematic care (interventional group). Patients randomized to the interventional group will be included in a protocol of daily automatic telemonitoring of arterial pressure, peripheral oximetry, heart rate and weight, and telematic consultations lead by a heart failure clinical specialized team.

Researchers will compare the healthcare resource utilization, healthcare and non-healthcare costs of patients randomized to control vs. interventional group.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Diagnosis of HF according to the 2021 guidelines of the European Society of Cardiology criteria for ≥3 months.
  • Admitted for decompensation of chronic HF.
  • Admitted for HF decompensation ≥30 days and ≤6 months.
  • HF decompensation in ≥30 days and ≤6 months but discharged directly from the emergency department or managed on an outpatient basis, but requiring intravenous diuretic administration in an ambulatory basis, or >50% increase in loop diuretic dose.
  • With previous optimized prognostic medical treatment.
  • Under treatment with loop diuretic drugs.
  • New York Heart Association functional class II, III or IV.

排除标准

  • Inclusion in other intervention studies.
  • Hemodynamic instability.
  • Acute myocardial infarction, acute pulmonary thromboembolism or stroke in the previous 40 days.
  • Uncontrolled arrhythmias
  • On waiting list for transplantation (any organ) or other cardiac surgery.
  • Advanced mechanical circulatory support.
  • Chronic renal disease on hemodialysis.
  • Life expectancy less than 1 year.
  • Moderate-severe cognitive impairment.
  • Manifest inability to use a technological system.
  • Institutionalized.
  • Limiting psychiatric pathology.

研究组 & 干预措施

Telemonitoring group

Experimental

Follow-up group by telematic consultations and non-invasive daily telemonitoring of weight, blood pressure, heart rate, peripheral oxygen saturation and electrocardiogram.

干预措施: Telemonitoring follow-up using medical devices and telematic consultations (Other)

Control gropu

No Intervention

Usual care follow-up group

结局指标

主要结局

Health care costs

时间窗: 12 months

Sum of the costs for the consumption of medicines, primary care consultations, specialist consultations, hospitalization, emergency care and medical transport.

次要结局

  • Non-health care costs(12 months)
  • Symptoms(12 months)
  • Number of hospital admissions(12 months)
  • Mortality(12 months)
  • Care burden of caregivers(12 months)
  • Patient satisfaction with service(12 months)
  • Adherence to the telemonitoring protocolo(12 months)
  • Quality of life variation(12 months)

研究者

发起方
Hospital Universitario 12 de Octubre
申办方类型
Other
责任方
Principal Investigator
主要研究者

Juan Carlos López-Azor

Principal Investigator, Doctor in Medicine

Hospital Universitario 12 de Octubre

研究点 (1)

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