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临床试验/NCT03234023
NCT03234023已完成不适用

A Remote Nursing-Guided Secondary Prevention Programme in Acute Coronary Syndrome. The SPRING Randomized Controlled Trial

University Hospital A Coruña4 个研究点 分布在 1 个国家目标入组 484 人开始时间: 2017年10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
484
试验地点
4
主要终点
major adverse events

研究概览

简要总结

DESIGN: Controlled clinical trial with single randomization, unmasked, open and multicentric.

CENTERS: University Hospital of A Coruña and University Hospital of Ferrol CONDITION TO STUDY: Acute Coronary Syndrome (ACS). INTERVENTION:monitored outhospital not inhospital supervised. MAIN OBJECTIVE: To determine the incidence of major adverse events (total mortality, new ACS, coronary revascularization, all-cause hospitalization) during the one-year period after hospitalization for ACS.

详细描述

The SPRING study aims to learn whether a remote, nurse-guided secondary prevention program reduces adverse events in patients who suffer an infarction during the subsequent one-year period. The SPRING study focuses not only on adverse events but also on the patients' state of life in terms of diet, physical exercise, emotional state, tobacco use, and adherence to medical treatment. Nursing is a profession in charge of preserving the health of patients, which is why the remote secondary cardiovascular prevention program of this study is coordinated by a nurse.

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
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All patients who have suffered an ACS in the health area of A Coruña or Ferrol from the beginning of the study inclusion period until reaching the fixed sample size.
  • Ages between 18 and 75 years.
  • Patients with ability to read and understand the participation sheet in the study.
  • Patients signing informed consent to participate in the study.
  • Patients living in the health care area of HUAC or HUF.

排除标准

  • Patients who are dependent for the Basic Activities of Daily Living (BADL) or who suffer from severe cognitive impairment (which makes reliable anamnesis impossible).
  • Patients with a Left Ventricular Ejection Fraction (LVEF) less than or equal to 35%.
  • Patients with a NYHA III / IV score and / or the Canadian Cardiovascular Association (CCS) scale of IV.

结局指标

主要结局

major adverse events

时间窗: 1 year

total mortality, new ACS, coronary revascularization, hospitalization for any cause

次要结局

  • cardiovascular mortality(1 year)
  • cardiovascular hospitalization(one year)
  • stroke(1 year)
  • tobacco(1 year)
  • physical activity(1 year)
  • nutrition(1 year)
  • emotion state(1 year)

研究者

发起方
University Hospital A Coruña
申办方类型
Other
责任方
Principal Investigator
主要研究者

CARMEN NERI FERNANDEZ POMBO

Research Nurse.

University Hospital A Coruña

研究点 (4)

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