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临床试验/NCT04462224
NCT04462224Unknown不适用

Creation of Home-based Asthma Real-World Measures With Mobile Health (CHARM) Study

National Jewish Health1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2021年1月11日最近更新:
适应症

试验速览

阶段
不适用
入组人数
150
试验地点
1
主要终点
Change from baseline in Asthma Control Test

研究概览

简要总结

Four novel biologic therapies (benralizumab, dupilumab, mepolizumab, reslizumab) have been recently approved for moderate-to-severe, eosinophilic or oral steroid-dependent asthma. The efficacy and safety of these therapies have been determined primarily by randomized clinical trials that compared annualized rates of significant asthma exacerbations (SAEs), lung function changes, and standardized symptom survey score changes in therapy-treated subjects in comparison to placebo matched controls. Yet, there is increasing interest to assess the efficacy, health benefits, and safety in medical therapies using real-world evidence (RWE). Further, home monitoring of asthma using mobile health (mHealth) technology may help scientists develop new and more sensitive indicators of asthma control that could improve clinical care. The hypothesis is that real world evidence, collected at home using several mobile health technologies, will help determine the efficacy, health benefits, and side effects of these therapies.

Objectives

  1. Assess real-world evidence (RWE) indicators of worsening and improving asthma. Scientists will measure steps per day, duration and vigor of exercise per day, sleep quality, and the number of awakenings per night using Fitbit activity trackers. Scientists will measure symptoms using once-monthly custom survey delivered to participant smartphones via Twilio. Rescue medication use and adherence to maintenance medications may be measured using digital inhaler devices. Adherence to biologic use using HealthBeacon smart sharps containers may be measured. Measures collected will be correlated to patient-reported significant asthma exacerbations (SAEs), lung function (FEV1), and the asthma control test (ACT) collected in clinic every 3 months.
  2. Use RWE to determine responses to biologic therapies. Scientists will combine at-home and clinic data to determine responses to biologics.

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 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • A diagnosis of uncontrolled or difficult-to-treat asthma, defined as 1 course of systemic corticosteroids (e.g. oral prednisone) in the last 12 months
  • An asthma control test (ACT) score less than or equal to 19 despite regular use of inhaled corticosteroids (ICS) therapy (at least 176 mcg of fluticasone/day or the equivalent)
  • Participants will need access to a smartphone (As of January 2018, ~ 80% of U.S. adults owned a smartphone (Mobile Fact Sheet, 2018))

排除标准

  • Active smoking
  • Any significant comorbid conditions that could inadvertently interfere with study results (i.e. any terminal illness, cancer, HIV, end-stage renal disease, congestive heart failure, severe autoimmune disease or inflammatory bowel disease)
  • Conditions that require bursts of oral corticosteroids
  • Other significant lung diseases (cystic fibrosis, pulmonary hypertension, interstitial lung disease, pulmonary fibrosis among others) to be determined by the investigators.

结局指标

主要结局

Change from baseline in Asthma Control Test

时间窗: Baseline to 24 or 52 weeks

Standardized asthma symptom survey

次要结局

  • Change From Baseline in Number of Puffs per Day of Beta Agonist Rescue Medication(Baseline and Week 24 (Phase 1) or Week 52 (Phase 2))
  • Change From Baseline in Duration of Interrupted Sleep per Night(Baseline and Week 24 (Phase 1) or Week 52 (Phase 2))
  • Change From Baseline in Lung Function(Baseline and Week 24 (Phase 1) or Week 52 (Phase 2))
  • Change From Baseline in Adherence of Inhaled Corticosteroids(Baseline and Week 24 (Phase 1) or Week 52 (Phase 2))
  • Change From Baseline in Adherence of Biologics(Baseline and Week 24 (Phase 1) or Week 52 (Phase 2))
  • Change From Baseline in Duration and Intensity of Exercise Per Day(Baseline and Week 24 (Phase 1) or Week 52 (Phase 2))
  • Change From Baseline in the Monthly Symptom Questionnaire Scores(Baseline and Week 24 (Phase 1) or Week 52 (Phase 2))
  • Change From Baseline in Significant asthma exacerbations(Baseline and Week 24 (Phase 1) or Week 52 (Phase 2))
  • Change From Baseline in Steps Per Day(Baseline and Week 24 (Phase 1) or Week 52 (Phase 2))
  • Change From Baseline in Number of Awakenings per Night(Baseline and Week 24 (Phase 1) or Week 52 (Phase 2))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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