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临床试验/NCT04955080
NCT04955080已完成不适用

REal-time Data Monitoring for Shared Adaptive, Multi-domain and Personalised Prediction and Decision Making for Long-term Pulmonary Care Ecosystems (RE-SAMPLE)

Medisch Spectrum Twente1 个研究点 分布在 1 个国家目标入组 216 人开始时间: 2022年1月24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
216
试验地点
1
主要终点
Predictors for exacerbations of COPD and comorbidities

研究概览

简要总结

The main objective of this RE-SAMPLE cohort study is to identify from a real-world data (RWD) set that will be collected, a subset of data that can be potentially used as important predictors and parameters for disease progression of COPD and complex chronic conditions, and multi-morbid exacerbations. The secondary objective is to evaluate the feasibility of RWD collection from a patient's perspective.

Study design: This is a prospective observational cohort study to collect RWD in patients with COPD and complex chronic conditions, with a maximum of 38 months of follow-up. Measurements are performed and RWD are collected by using the Healthentia mobile phone application at baseline (e.g. patient characteristics), daily (e.g. symptom diary), during follow-up visits and at deterioration, and from hospital data (e.g. healthcare visits). The choice of parameters and measurement tools that will be collected during the cohort will be updated every three months during the first year of the cohort (via protocol amendments). These updates are based on citizen-design sessions and on new literature insights. Prognostic models will be developed including predictors derived from the RWD collection.

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

入选标准

  • Clinical diagnosis of COPD according to the GOLD criteria [5] (FEV1 < 80% of the predicted value and FEV1/FVC < 0.70);
  • Patients can be included both at stable state and during exacerbation/hospitalization;
  • At least one comorbidity:
  • diabetes mellitus (glucocorticoid-induced, or stable type 1 or 2), chronic heart failure (clinical diagnosis according to the ESC guidelines), ischaemic heart disease (history of myocardial infarction, angina pectoris), active symptoms of anxiety and/or depression (≥11 Hospital Anxiety and Depression Scale , and/or anxiety or depression symptoms being treated at the time of inclusion);
  • Under treatment at one of the pilot sites (MST, TUK, GEM);
  • >40 years of age;
  • Smoker or ex-smoker;
  • Able to understand, read and write the language spoken in the country of the pilot site.
  • Accessibility to internet;
  • Written informed consent from the subject prior to participation.
  • Furthermore, 25% of the patients should also have ≥ 2 exacerbations, defined as respiratory problems that required a course of oral corticosteroids / antibiotics in the two years preceding study entry; and/or ≥ 1 hospitalisation for respiratory problems in the two years preceding study entry; and/or modified MRC (mMRC) score of 3 or 4 (COPD patients with these scores have a higher chance of exacerbating).

排除标准

  • Serious other diseases with a low survival rate;
  • Presence of any other active lung disease (e.g., sarcoidosis);
  • Severe psychiatric illness, diagnosed by anamnesis;
  • Maintenance therapy with antibiotics
  • Patients with cognitive impairment (Mini Mental State Examination (MMSE) < 24)

结局指标

主要结局

Predictors for exacerbations of COPD and comorbidities

时间窗: Through study completion, an average of 2.5 years.

Prognostic performance of the validated predictive model for COPD and comorbid exacerbations and disease progression from RWD. The measures for progression will be survival, based on all-cause mortality, as well as morbidity. Morbidity is defined as time until first hospitalisation for an acute exacerbation of COPD and CCC, time until first moderate COPD exacerbation, time until first pneumonia, and total number of COPD and CCC exacerbations (extracted from daily symptom diaries) and pneumonia.

次要结局

  • Feasibility of the RWD collection.(Through study completion, an average of 1 year)

研究者

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

Job van der Palen

PhD

Medisch Spectrum Twente

研究点 (1)

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