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临床试验/NCT01683903
NCT01683903Unknown不适用

Comparison of Cardiac Rehabilitation Benefits Between Coronary and Non-coronary Patients Through a 24 Months Follow-up : the "INCARD" Study

Centre Hospitalier Sud Francilien1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2012年8月最近更新:
适应症

试验速览

阶段
不适用
入组人数
150
试验地点
1
主要终点
Change in VO2max every 6 months over the 24 months

研究概览

简要总结

Treatment of chronic heart failure requires multidisciplinary approaches with a recognized role for cardiac rehabilitation. Rehabilitation helps to improve patient's functional, decrease morbidity and mortality, decrease rehospitalization rate, thereby reducing costs of this disease. After recovery from the acute phase of cardiac infarction, patients admitted to the rehabilitation center will follow the usual rehabilitation program during the hospitalization period. This step precludes outpatient follow-up period in our day hospital, in accordance with their physicians and cardiologists who manage the monitoring. The study INCARD (Insuffisance Cardiaque en Readaptation Durable) will be developed to evaluate the benefits of a sustainable rehabilitation heart failure on patients treated optimally and educated during a follow-up period of 24 months. The main objective of the study will be to compare the benefits of rehabilitation between coronary (C) and non-coronary (NC) patients for each evaluation time point, periodically recorded

详细描述

We will undertake a prospective follow-up study of 150 rehabilitated patients with heart failure (75 C; 75 NC). The main objective will be to compare the benefits of rehabilitation between coronary and non-coronary patients based on functional improvement i.e. improvements of VO2max, LVEF (ultrasound method and/or isotopic), 6-min walk test, Minnesota index of quality of life. In addition, clinical outcomes (HR, SBP, DBP, BMI) and paraclinical data (creatinine clearance) will be measured as patients' standard clinical follow-up .

Clinical data of the patients admitted to the cardiac rehabilitation, including heart failure patients (LVEF <40), will be recorded after collection of their signed informed consent agreement. Patients will be addressed from heart failure intensive care units for coronary (USIC) or acute cardiac services to the rehabilitation department. Patients will be admitted in the rehabilitation department when there are clinically stable (at least three weeks after the acute episode). Etiology of the heart failure will be assessed and patients stratified as C or NC patients.

Expected Results We will estimate the mean duration of inpatient rehabilitation (H period). Then, we will follow patients' cardiac evaluation parameters recorded from an outpatient follow-up, first 3 months after inclusion and then every 6 months over the 24 months of outpatient follow-up.

These data will allow for comparison of the benefits of rehabilitation between coronary (C) and non-coronary (NC) patients for each evaluation time point and will give information on the clinical improvement of each group of patients.

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

入选标准

  • Age over 18 years old,
  • Signed informed consent,
  • Patients with left ventricular ejection fraction below 40 %,
  • Stable for over 3 weeks,
  • Known etiology,
  • Able to do the performance test on treadmil or bicycle in order to have rehabilitation.
  • No clinical avoidance reasons.
  • Patient with health care registration.
  • Agreement from the general practictioner and from the cardiologist that follows the patient.

排除标准

  • Age below 18 years old,
  • Unstable heart failure,
  • Unable to do a performance test as indicated above,
  • Patients not able to understand clinical counseling.
  • Patient under tutella.
  • Pregnancy.

结局指标

主要结局

Change in VO2max every 6 months over the 24 months

时间窗: every 6 months over the 24 months of outpatient follow-up

VO2max (L)

Change in Left ventricular ejection fraction every 6 months over the 24 months of outpatient follow-up

时间窗: every 6 months over the 24 months of outpatient follow-up

Left ventricular ejection fraction (ultrasound method and/or isotopic) in %

Change on 6-min walk test every 6 months over the 24 months

时间窗: every 6 months over the 24 months of outpatient follow-up

6-min walk test (m)

Change on Minnesota index of quality of life every 6 months over the 24 months

时间窗: every 6 months over the 24 months of outpatient follow-up

Minnesota index of quality of life.

Change on heart rate every 6 months over the 24 months

时间窗: every 6 months over the 24 months of outpatient follow-up

Heart rate (bpm)

Change on systolic blood pressure every 6 months over the 24 months

时间窗: every 6 months over the 24 months of outpatient follow-up

systolic blood pressure (mmHg)

Change on diastolic blood pressure every 6 months over the 24 months

时间窗: every 6 months over the 24 months of outpatient follow-up

diastolic blood pressure (mmHg)

Change on body mass index every 6 months over the 24 months

时间窗: every 6 months over the 24 months of outpatient follow-up

Measurement of weight and height, calculation of body mass index (kg/m2)

Change on creatine clearance every 6 months over the 24 months

时间窗: every 6 months over the 24 months of outpatient follow-up

creatine clearance (ml/min)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

KOUKOUI Francois

MD

Centre Hospitalier Sud Francilien

研究点 (1)

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