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临床试验/NCT05309356
NCT05309356招募中不适用

IMplementing Predictive Analytics Towards Efficient COPD Treatments (IMPACT) Study

University of British Columbia4 个研究点 分布在 1 个国家目标入组 1,130 人开始时间: 2023年3月21日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
1,130
试验地点
4
主要终点
Prescription appropriateness

研究概览

简要总结

Chronic Obstructive Pulmonary Disease (COPD) is a chronic disease of the lungs that affects more than 2.5 million Canadians. Patients with COPD experience episodes of lung attacks (or exacerbations). During these attacks, patients experience an intense increase in symptoms, such as breathlessness and cough. It is challenging to decide which patients should be put on treatments that would reduce the risk of such lung attacks. The digitization of health records in many clinics and hospitals means complex risk prediction algorithms can be used to predict the risk of lung attacks to enable personalized care. In this study, our team will implement a risk prediction tool (called ACCEPT) into the electronic health records in two teaching hospitals in Vancouver, British Columbia (BC), Canada. A clinical study will be conducted to evaluate if the use of this tool results in patients with COPD receiving better care with better outcomes, and if they are more satisfied with the care they are receiving.

详细描述

COPD is a heterogenous and progressive disease of the airways that affects millions of people worldwide. However, current treatment guidelines fail to provide personalised, patient-centered disease management. In contrast, precision medicine emphasizes the tailoring of disease management to patient characteristics and values to optimize patient care and outcomes. Clinical prediction models (CPMs) are major enablers of precision medicine, and facilitate targeted therapies to patients who will benefit the most from them.

The investigators developed a CPM called ACCEPT that improves risk stratification for COPD patients by predicting the risk of exacerbation at an individual level and thereby enabling personalized, preventive disease management. Using a stepped wedged cluster randomized controlled trial (RCT), the investigators aim to evaluate the impact of integrating ACCEPT into routine COPD care at two outpatient respiratory clinics in Vancouver, British Columbia, Canada.

The 'stepped wedged' RCT has a cross-over design, with treatment assignment done in a uni-directional, staggered format that will provide opportunities to control for time trend. The total duration of the study is 30 months. There will be a one-month phase in period with patient recruitment and data collection starting on month two. The last physician assignment will occur in month 18, and patient recruitment will continue until month 24. Follow-up data will be collected until month 30 to ensure six months of follow-up data for all patients.

Primary and secondary outcomes will be analysed using generalized estimating equations to account for possible clustering of endpoints (multiple visits for each physician). Further, following the intention to treat principle, clusters (physicians) will be analyzed according to their randomized crossover time irrespective of whether crossover was achieved at the desired time.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
35 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Are a legal Canadian resident
  • Aged 35 years and older
  • Can speak English
  • Have a diagnosis of COPD

排除标准

  • Are under 35 years of age

结局指标

主要结局

Prescription appropriateness

时间窗: Cross-sectional: data collected during each patients initial study visit for the duration of the trial (24 months)

Binary variable indicating the concordance between the physician- and ACCEPT-based treatment recommendations (0: discordant prescription, 1: concordant prescription). We will compare the percentage of prescription appropriateness between the two study arms. The prescription recommended by the physician during the clinical encounter will be recorded. After the encounter, a research coordinator will interview the patient, use ACCEPT to produce the ACCEPT-based optimal treatment for the patient. The physician prescription will be considered concordant if it is the same as the prescription based on the ACCEPT recommendation (or if ACCEPT suggests more than one eligible prescription, the physician prescription is one of them), otherwise it will be considered discordant.

次要结局

  • COPD patient's Quality of Life(EQ5D will be administered at baseline (study visit 1, day 1), month 3, and month 6)
  • Impact of COPD on patient's daily life(CAT will be administered at baseline (study visit 1, day 1), month 3, and month 6)
  • Rate of moderate or severe exacerbations(1 year before and 1 year after initial study visit.)
  • Self-reported medication adherence and beliefs(BMQ-COPD will be administered at baseline (study visit 1, day 1), month 3, and month 6)
  • Medication adherence(1 year before and 1 year after initial study visit (day 1).)

研究者

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

Mohsen Sadatsafavi

Principal Investigator

University of British Columbia

研究点 (4)

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