跳至主要内容
临床试验/NCT02522182
NCT02522182已完成不适用

ALLiance for SEcondary PREvention After an Episode of Acute Coronary Syndrome. the ALLEPRE Trial: a Fully Nurse-led Intensive Intervention Programme

Azienda Ospedaliero-Universitaria di Parma7 个研究点 分布在 1 个国家目标入组 2,060 人开始时间: 2012年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
2,060
试验地点
7
主要终点
The difference in the degree of adherence to the goals concerning risk factors, lifestyle modifications and pharmacological therapy.

研究概览

简要总结

The purpose of the ALLEPRE trial is to compare the benefit offered by a structured, intensive and fully nurse-led intensive secondary prevention intervention programme with that offered by standard of care in a high-risk population of patients admitted to hospital because of an ACS.

详细描述

ALLEPRE enrols a population of residents in Emilia Romagna with a diagnosis of ACS (unstable angina, non-ST segment elevation myocardial infarction, ST segment elevation myocardial infarction) who were admitted to the specialist cardiological departments of the participating centres up to 20 days after the index event.

All eligible patients are randomised 1:1 to the nurse-led intensive secondary prevention programme (ISPP: intervention/experimental arm) or usual treatment (UT: control arm).

Randomisation is centralised by means of IVRS under the responsibility of the Study Coordinator and the Principal Investigator at each hospital centre, and the patients are the allocated to groups by e-mail. Due to the nature of the study, neither participants nor research personnel can be blinded to the group assignments. The randomisation data are kept at the coordinating centre.

OPERATIVE PHASE After randomisation, all of the patients in both arms undergo a baseline examination and are required to return to their reference centre for follow-up visits after 12, 24 and 60 months for outcome assesment. Outcomes will also be recorded after 36 and 48 months on the basis of telephone enquiries.

ISPP: intervention arm. This consists of a series of programmed sessions involving the centrally trained nurses and the patients randomised to the ISPP. There will be a total of nine sessions: before discharge, and one, three, six, 12, 18, 24, 36 and 48 months after discharge. During the sessions, each of which will last for about one hour, the trained nurse will record the main clinical parameters (i.e. risk factors, lifestyle habits, adherence to therapy, and any discrepancies between patient reports and the recommended goals) using an ad hoc clinical file (SIM: scheda infermieristica multidimensionale or multidimensional nursing form), and then activate the interventions laid down by the pre-specified rules inside the SIM in order to correct the discrepancies. The activation of the pre-established multidisciplinary network (anti-smoking, anti-diabetes and anti-hypertension centres, and psychological support) is completely under the nurses' control.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Eligible patients aged >18 years with an ACS (unstable angina, non- ST-segment elevation myocardial infarction [MI], or ST-segment elevation MI [International Classification of Diseases, Ninth Revision, Clinical Modification codes 41071, 41001, 41011, 41021, 41031, 41041, 41051,41061, 41081, and 41091]) who are admitted to the Cardiological Divisions of the 6 participating centers in Emilia-Romagna (Italy) are considered for enrolment for up to 20 days after the index event and before being discharged.

排除标准

  • •Once it has been verified that the patients are capable of participating in a prospective study, the only exclusion criterion is a life expectancy of b12 months because of a severe noncardiac disease

研究组 & 干预措施

Intensive Secondary Prevention Programme

Experimental

The Nurse-led Intensive Secondary Prevention Programme consists of programmed 9 sessions involving the trained nurses and the patients randomised to the experimental programme: before discharge, and one, three, six, 12, 18, 24, 36 and 48 months follow up. During the sessions the nurse will record the main clinical parameters (risk factors, lifestyle habits, adherence to therapy, psychological characteristics), any discrepancies between patient reports and the recommended goals and then activate the interventions in order to correct the discrepancies. The activation of the pre-established multidisciplinary network (anti-smoking, anti-diabetes and anti-hypertension centres, and psychological support) is completely under the nurses' control.

干预措施: Nurse-led Intensive Secondary Prevention Programme (Behavioral)

Usual Treatment

Active Comparator

The patients randomised to the control group will follow the Usual Treatment for secondary prevention of the hospital to which they were admitted

干预措施: Usual Treatment (Behavioral)

结局指标

主要结局

The difference in the degree of adherence to the goals concerning risk factors, lifestyle modifications and pharmacological therapy.

时间窗: 24 months

Adherence to the goals of classic cardiovascular risk factors: - number of patients (nop) with systolic blood pressure \<140 mmHg, divided by total nop.

Major adverse events

时间窗: 5 years

Composite of cardiovascular mortality, non-fatal reinfarction, non-fatal stroke

次要结局

  • Clinical endpoints(5 years)

研究者

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

Diego Ardissino

MD

Azienda Ospedaliero-Universitaria di Parma

研究点 (7)

Loading locations...

相似试验