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临床试验/NCT03645564
NCT03645564终止不适用

Impact of the Information Follow-up Given to Patients on Their Disease Understanding and Therapeutic Adherence in Patients Under Direct Oral Anticoagulants and With Atrial Fibrillation in a Cardiology Department

University Hospital, Bordeaux2 个研究点 分布在 1 个国家目标入组 221 人开始时间: 2018年10月16日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
221
试验地点
2
主要终点
Adherence to direct oral anticoagulants

研究概览

简要总结

The primary objective of this study is to measure in patients addressed for Atrial Fibrillation (AF) in the Cardiology-Electrophysiology and Cardiac Stimulation Department of Bordeaux hospital, the impact of a specialized nurse consultation on their adherence level to direct oral anticoagulants treatments.

详细描述

The number of persons that should take an anticoagulant treatment in France is evaluated at 3 Billion and at least half of them for an Atrial Fibrillation disease. One of the main issues of their prescription is stoke prevention. With the coming of direct oral anticoagulants, which does not require repeating controls like it is the case for anti-vitamin K treatments, the patient's involvement is a guarantee of therapeutic adherence and good use. Nevertheless a good adherence level is seldom reached. This highlights the importance of individualized information which must be followed for purposes of accuracy and deepening. Thus as part of investigator's activity department that treats about 1000 patients per year for an Atrial Fibrillation, the information, use and therapeutic adherence are a priority in the care pathway of patients under direct oral anticoagulants. The investigators propose to measure the contribution of a specialized nurse consultation in contact with a multidisciplinary team on therapeutic adherence. The investigators hypothesis that an individualized and reassessed information would allowed a better understanding by the patients of their pathology and care and thus a better therapeutic adherence. A control group will present the same care pathway than all the patients of the service suffering from Atrial Fibrillation without specialized nurse consultation. The second group will benefit of a specialized nurse consultation throughout of which an individualized information will be delivered. This information will be reevaluated during the usual patient follow-up. All the patients will be followed at 3 months, 6 months and 1 year as part of the usual care of the service.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

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

入选标准

  • Patient hospitalized in the Cardiology-Electrophysiology and Cardiac Stimulation Department for an AF,
  • Patient requiring direct oral anticoagulant treatment,
  • Age ≥ 18 years of both genders,
  • Written consent,
  • Patient affiliated or beneficiary of a social insurance,
  • French language.

排除标准

  • Patient unable to give his written consent or with cognitive disorders,
  • Patient depending of a third person,
  • Patient unable to be followed in the service,
  • Patient in exclusion period for another protocol,
  • Subject deprived of liberty by judicial or administrative decision,
  • Protected adults,
  • Non-inclusion criteria specific to direct oral anticoagulants (valvular AF, severe renal impairment).

结局指标

主要结局

Adherence to direct oral anticoagulants

时间窗: 12 months

Adherence questionnaire

次要结局

  • Change in the level of knowledge of disease and treatment(Change from baseline at 12 months)

研究者

发起方
University Hospital, Bordeaux
申办方类型
Other
责任方
Sponsor

研究点 (2)

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