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临床试验/NCT03838003
NCT03838003已完成不适用

Rehabilitation Nursing on Patients Admitted by Recently Decompensated Heart Failure (ERIC Program) - Impact of Exercise

Universidade do Porto2 个研究点 分布在 1 个国家目标入组 250 人开始时间: 2017年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
250
试验地点
2
主要终点
6 minute walking test

研究概览

简要总结

An aerobic physical exercise protocol will be applied to patients admitted in ward due to decompensated heart failure, in order to validate the efficacy and safety of physical exercise in this phase of clinical stabilization, through the said training protocol - ERIC program.

详细描述

With the objective of validating the efficacy and safety of physical exercise as a therapeutic resource in patients admitted for decompensated heart failure; will be applied, by rehabilitation nurses, a protocol of physical exercise, with increasing levels of intensity. Patients who meet the inclusion criteria will be randomized through an online program (randomizer.org) and the ERIC protocol will be applied to the test group. The control group will be implemented the usual care of rehabilitation nursing. The ERIC protocol comprises 5 levels of intensity, as following shown: Stage 1 - respiratory and calisthenic exercises (5-10 minutes) Stage 2 - pedal for 5-10 minutes Stage 3 - aerobic training: walking on the corridor for 5-10 minutes Stage 4 - aerobic training: walking on the corridor for 10-15 minutes Stage 5 - aerobic training: walking on the corridor for 15 minutes + climbing stairs for 5 minutes All patients will be monitored and followed up by a rehabilitation nurse while they are doing the exercise. The investigator decides, depending on the patient's performance and clinical conditions, the form of progression in the program, but it is mandatory to follow the previously defined levels of intensity.

Patients in the test group may start the program only on stage I or II according to clinical criteria. At admission of the patients (test group and control group) clinical and sociodemographic parameters are evaluated, as well as data related to Barthel's indices and London Chest of activities of daily living (LCADL). At the discharge date, the Barthel index and the LCADL scale will also be evaluated, as well as the 6-minute walking test.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

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

  • Admission diagnosis of Decompensated heart failure
  • More than 18 years old
  • Capacity to provide informed consent

排除标准

  • Osteoarticular pathology that impedes the performance of the exercise
  • Existence of inotropic infusions
  • Dysrhythmia or precordial pain in the last 24 hours
  • Acute pulmonary edema in the last 12 hours
  • Systolic blood pressure greater than 180millimetre of mercury (mmHg) or less than 80mmHg (except in cases where this is the baseline value for the patient)
  • Need for oxygen at a rate greater than 3 /min
  • Glycemic decompensation in the last 12 hours

结局指标

主要结局

6 minute walking test

时间窗: through study completion, an average of 1 year

Number of meters walked in the 6 minute walking test

次要结局

  • Number of dysrhythmias during exercise in the training group(through study completion, an average of 1 year)
  • Number of falls during exercise in the training group(through study completion, an average of 1 year)
  • Number of chest pain situations during exercise in the training group(through study completion, an average of 1 year)
  • Barthel Index score(through study completion, an average of 1 year)
  • London Chest Activity of Daily Living (LCADL) scale score(through study completion, an average of 1 year)
  • Number of emergency situations during exercise in the training group(through study completion, an average of 1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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