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临床试验/NCT03420235
NCT03420235已完成不适用

Home Monitoring in Idiopathic Pulmonary Fibrosis; Improving Use of Anti-fibrotic Medication and Quality of Life

Erasmus Medical Center2 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2018年1月9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
90
试验地点
2
主要终点
Difference in the change in total score of King's brief Interstitial Lung Disease Health Status (K-BILD) questionnaire between the home monitoring group and the standard care group

研究概览

简要总结

In this study it will be investigate whether a home monitoring program improves disease-specific health-related quality of life (HRQOL) for patients with idiopathic pulmonary fibrosis (IPF) through appropriate medication use and subsequently results in better objective and subjective outcomes.

详细描述

IPF is a chronic disease with progressive scarring of the lung tissue (fibrosis), resulting in a poor prognosis and a devastating impact on the lives of patients and their families. Progressive shortness of breath, cough and fatigue are major factors influencing health-related quality of life (HRQOL) in patients with IPF. Recently two anti-fibrotic drugs became available that slow down disease progression. The availability of effective drugs for this devastating disease has importantly changed daily care and research in IPF. Currently, one of the major challenges in daily IPF care is the evaluation of how individual patients objectively and subjectively experience treatment and benefit from treatment. The use of information communication technology in health care, also named e-health, is a promising solution to improve the quality of care. E-health allows remote exchange of data between patients and health care professionals which enables monitoring, research and management of long term conditions. Also communication between patients and physicians, and physicians mutually, becomes more accessible. This creates an opportunity for earlier intervention by health care professionals, which may prevent a hospital admission. This might improve quality of life and reduce costs. Patients easily get access to up-to-date and tailored information, in an interactive way. By providing these tools, patients may better understand their health conditions and become actively involved in management of their own health care, which may lead to a better health status. An 'internet tool' for patients with IPF have been developed, providing information and enabling them to keep track of their own symptoms, HRQOL scores, medication use and lung function results.

In this study it will be investigated whether a home monitoring program improves disease-specific HRQOL for IPF patients through appropriate medication use and subsequently results in better objective and subjective outcomes.

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
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

入选标准

  • All patients with a diagnosis of IPF according to the ATS 2011 criteria and about to start on anti-fibrotic treatment (either nintedanib or pirfenidone)

排除标准

  • Not able to speak, read or write in Dutch
  • No access to internet

结局指标

主要结局

Difference in the change in total score of King's brief Interstitial Lung Disease Health Status (K-BILD) questionnaire between the home monitoring group and the standard care group

时间窗: 24 weeks after inclusion

Change in HRQOL assessed by the K-BILD, between control group and home monitoring group at the end of the study. The K-BILD is a 15-item self-administered questionnaire on a 7-point response scale. It has three domains: breathlessness and activities, psychological and chest symptoms.The domain and total score ranges are 0-100, with the higher scores corresponding with better HRQL.

次要结局

  • Patient satisfaction with the care process(24 weeks after inclusion)
  • FVC decline(24 weeks after inclusion)
  • Difference in the change in total score of King's brief Interstitial Lung Disease Health Status (K-BILD) questionnaire between the home monitoring group and the standard care group(12 weeks after inclusion)
  • Number of patients who discontinue use of medication, pills used and pills wasted(24 weeks after inclusion)
  • Amount of contacts with healthcare providers and number of visits per patient(24 weeks after inclusion)
  • Patient-reported outcome (PRO) scores (HADS)(24 weeks after inclusion)
  • Patient expectations and satisfaction with medication (PESaM scores)(Baseline and 24 weeks after inclusion)
  • Personal goal of patient defined at start of study(24 weeks after inclusion)
  • Patient-reported outcome (PRO) scores (GRC)(24 weeks after inclusion)
  • Patient-reported outcome (PRO) scores (EQ5D)(24 weeks after inclusion)
  • Patient satisfaction with medication (PESaM scores)(24 weeks after inclusion)

研究者

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

Marlies Wijsenbeek

Dr. M.S. Wijsenbeek, pulmonologist, Principal Investigator

Erasmus Medical Center

研究点 (2)

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