NL-OMON52658已完成4 期
A cluster Randomised Controlled Trial of the effectiveness, usability and acceptability of a smart inhaler programme in asthma patients: the ACCEPTANCE study - ACCEPTANCE study
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 242
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Age >= 18 years;
- •Doctor-diagnosed asthma (according to Dutch national primary care asthma
- •guidelines (NHG)) - route A and B; Self-reported asthma diagnosis (confirmed at
- •study end (T12) by GP) - route C;
- •Partially controlled or uncontrolled asthma (ACQ >= 0.75);
- •Use of Symbicort Turbuhaler maintenance therapy;
- •Being 'non-adherent' defined as an adherence rate (number of fully adherent
- •days / total number of days) of below 80% over the 3rd and 4th week of the
- •run-in period.
排除标准
- •Use of SMART regimen (Symbicort Maintenance And Reliever Therapy) by taking
- •Symbicort as reliever in response to symptoms;
- •Change in inhaled corticosteroids dose in the 4 weeks prior to run-in period;
- •Use of systemic corticosteroids in the 4 weeks prior to run-in period;
- •Current use of biologics, (anti-IL-5 en anti-IgE);
- •Diagnosis of COPD or other significant respiratory diseases;
- •Malignancy with life expectancy < 1 year;
- •Inability to understand Dutch.
研究者
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