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临床试验/NCT03567785
NCT03567785已完成不适用

Supporting Adherence to Pirfenidone in Patients With Idiopathic Pulmonary Fibrosis: the Key to Successful Treatment Outcomes: the SUPIRIO-study

KU Leuven1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2018年7月17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
KU Leuven
入组人数
66
试验地点
1
主要终点
The prevalence of non-adherence to pirfenidone (=non-initiation, discontinuation and non-implementation).

研究概览

简要总结

Idiopathic pulmonary fibrosis (IPF) is an irreversible, chronic and relentless lung disorder of unknown aetiology leading ultimately to respiratory insufficiency and death within 2-5 years after diagnosis. Treatment with the anti-fibrotic drug Pirfenidone slows down the disease progression and reduces the risk of acute exacerbations. Unfortunately, Pirfenidone represents a complex pharmacological regimen, in which patients have to take 3 tablets 3 times a day at mealtime. As for all chronically ill patients, adherence to a complex regimen might be challenging and nonadherence might reduce the full potential of Pirfenidone in patients with IPF. Due to extremely sparse availability of evidence on treatment adherence in the IPF population, it needs to be fully ascertained if, why, when and how many patients discontinue treatment or struggle to correctly take Pirfenidone as prescribed.

详细描述

Idiopathic pulmonary fibrosis (IPF) is an irreversible, chronic and relentless lung disorder of unknown aetiology characterised by a progressive destruction of lung parenchyma leading ultimately to respiratory insufficiency and death within 2-5 years after diagnosis. Treatment with the anti-fibrotic drug Pirfenidone slows down the disease progression and reduces the risk of acute exacerbations. Evidence also showed that treatment with Pirfenidone should be continued lifelong to maximise outcomes even in patients who experience disease progression during therapy. Unfortunately, Pirfenidone represents a complex pharmacological regimen, in which patients have to take 3 tablets 3 times a day at mealtime with a titration period in the first 3 weeks (i.e. 3 times 1 tablet of 267 mg during the first week, 3 times 2 tablets during the second week, and 3 times 3 tablets a week from week 3 onwards). As for all chronically ill patients, adherence to a complex regimen might be challenging and nonadherence might reduce the full potential of Pirfenidone in patients with IPF. Adherence is defined as "the extent to which a person' s behaviour - taking medication, following a diet, and/or executing lifestyle changes, corresponds with agreed recommendations from a health care provider"(WHO, 2003) and encompasses three phases namely, initiation, implementation and persistence.

Due to extremely sparse availability of evidence on treatment adherence in the IPF population, it needs to be fully ascertained if, why, when and how many patients discontinue treatment or struggle to correctly take Pirfenidone as prescribed. Furthermore, the investigators also don't know what the impact is of non-adherence to Pirfenidone on clinical outcomes in patients with IPF and whether good adherence is associated with a better health related quality of life.

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

  • Clinical diagnosis of IPF based on the 2011 ATS/ERS/JRS/LATA diagnostic criteria
  • Patients who will start treatment with pirfenidone
  • Patients of 18 years or older
  • Oral fluency in Dutch or French
  • Being able to provide written informed consent

排除标准

  • Patients not managing their medications independently (e.g. Institutionalized patients, patients living in a nursing home or patients receiving homecare from a nurse). However, patients receiving help to prepare their medication from informal caregivers (i.e. family) are allowed to participate in the study.
  • Patients not having their follow-up consultations at the University hospitals of Leuven.

结局指标

主要结局

The prevalence of non-adherence to pirfenidone (=non-initiation, discontinuation and non-implementation).

时间窗: 1 year

All patients included in the study will be equipped with a Medication Event Monitoring System (MEMS) (Aardex, Ch) to monitor the medication adherence continuously and to characterise adherence patterns. The MEMS bottle contains a cap which holds a microchip and a pressure-release system that records and stores the exact time and date each time the patient opens the bottle.The monitoring device will be read by the investigator using the MedAmigoTM platform. Patterns of medication intake will be analysed by the investigator.

次要结局

  • Impact of medication non-adherence on the forced vital capacity (FVC).(1 year)
  • Impact of medication non-adherence on progression-free survival.(1 year)
  • Impact of medication non-adherence on quality of life measured with the EQ-5D-5L questionnaire.(1 year)
  • Impact of health literacy on therapy adherence.(Baseline)
  • Impact of depression on therapy adherence(1 year)
  • Impact of barriers on therapy adherence(1 year)
  • Impact of medication non-adherence on quality of life measured with the K-BILD questionnaire.(1 year)
  • Impact of medication non-adherence on quality of life measured with the SGRQ.(1 year)
  • Impact of non-adherence on the diffusing capacity for carbon monoxide (DLco).(1 year)
  • Adherence to Pirfenidone(1 year)
  • Knowledge that patients have on their disease and treatment(1 year)

研究者

发起方
KU Leuven
申办方类型
Other
责任方
Principal Investigator
主要研究者

Professor Wim Wuyts

Professor, Principal investigator

KU Leuven

研究点 (1)

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