Study protocol: a 52-week, multicentre, observational, prospective study on the use of a smart platform connected to a single-inhaler triple therapy (ICS/LABA/LAMA) to evaluate effectiveness on treatment adherence and inhaler technique in patients with poorly controlled asthma.

IF 3.1 3区 医学 Q2 RESPIRATORY SYSTEM
Jonas Aggerholm Baekdal, Nicolai Krogh, Gajanan Sakhare, Elisabeth Bendstrup, Charlotte Suppli Ulrik, Johannes Martin Schmid
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引用次数: 0

Abstract

Background: Good adherence to controller medication and correct inhaler technique is essential for effective asthma management. However, many patients struggle with these aspects, leading to poor symptom control and a higher risk of exacerbations. This study (SiASMARTer) aims to evaluate the impact of the SiA®SMARTer platform - a digital smart platform consisting of an app and an add-on module connected to a pressurized metered-dose inhaler delivering triple therapy (ICS/LABA/LAMA) - on improving adherence and inhaler technique in patients with poorly managed inflammation in asthma (defined as fractional exhaled nitric oxide [FeNO] > 25 ppb).

Methods: This observational study will enrol 60 patients from two sites in Denmark. At baseline, participants will begin using the SiA®SMARTer platform, which includes, on the patient side a smart inhaler cap, a patient app and on the physician side a dashboard. The primary endpoint, with follow-up at 12 and 52 weeks, is the platform's effect on FeNO levels. Secondary endpoints will include changes from baseline in treatment adherence and inhaler technique scores, Asthma Control Test scores, Mini Asthma Quality of Life Questionnaire scores, lung function parameters, FeNO category distribution, exacerbation rates, short-acting β2-agonist use, and patient-reported satisfaction with the SiA®SMARTer platform. Data on adherence and inhaler technique will be continuously collected through the SiA®SMARTer platform, and adverse events will be monitored.

Discussion: This study may offer valuable insights into whether a digital platform can enhance adherence and inhaler technique, and by that improve asthma control. Additionally, it may help discriminate patients requiring therapy escalation from those with poor control due to non-adherence or incorrect inhaler technique.

Trial registration: ClinicalTrials.gov identifier: NCT06908421, Registration date: 2025-03-26.

研究方案:一项52周、多中心、观察性、前瞻性研究,使用智能平台连接单吸入器三联疗法(ICS/LABA/LAMA),评估治疗依从性和吸入器技术对控制不良哮喘患者的有效性。
背景:良好的依从性控制药物和正确的吸入器技术对有效的哮喘管理至关重要。然而,许多患者在这些方面挣扎,导致症状控制不佳,病情恶化的风险更高。本研究(SiASMARTer)旨在评估SiA®SMARTer平台的影响,该平台是一个数字智能平台,由一个应用程序和一个连接到加压计量吸入器的附加模块组成,提供三联治疗(ICS/LABA/LAMA),改善哮喘炎症管理不良患者的依从性和吸入器技术(定义为分数呼出一氧化氮[FeNO] > 25 ppb)。方法:这项观察性研究将从丹麦的两个地点招募60名患者。在基线时,参与者将开始使用SiA®SMARTer平台,该平台包括患者侧的智能吸入器帽、患者应用程序和医生侧的仪表板。12周和52周随访的主要终点是该平台对FeNO水平的影响。次要终点包括治疗依从性和吸入器技术评分、哮喘控制测试评分、迷你哮喘生活质量问卷评分、肺功能参数、FeNO类别分布、加重率、短效β2激动剂使用和患者报告的SiA®SMARTer平台满意度的基线变化。依从性和吸入器技术的数据将通过SiA®SMARTer平台持续收集,并监测不良事件。讨论:这项研究可能为数字平台是否可以增强依从性和吸入器技术,从而改善哮喘控制提供有价值的见解。此外,它可能有助于区分需要升级治疗的患者与那些由于不遵守或不正确的吸入器技术而控制不良的患者。试验注册:ClinicalTrials.gov标识符:NCT06908421,注册日期:2025-03-26。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Pulmonary Medicine
BMC Pulmonary Medicine RESPIRATORY SYSTEM-
CiteScore
4.40
自引率
3.20%
发文量
423
审稿时长
6-12 weeks
期刊介绍: BMC Pulmonary Medicine is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of pulmonary and associated disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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