Svendsen Mathias Tiedemann, Andersen Flemming, Andersen Kirsten Hammond, Andersen Klaus Ejner
Department of Dermatology and Allergy Centre, Odense University Hospital, Kløvervænget 15, 5000, Odense C, Denmark.
Centre for Innovative Medical Technology, Institute of Clinical Research, University of Southern Denmark, Odense C, Denmark.
BMC Dermatol. 2018 Feb 7;18(1):2. doi: 10.1186/s12895-018-0071-3.
Topical corticosteroid or corticosteroid/calcipotriol preparations are recommended first-line topical treatments of psoriasis, but a main cause for the lack of efficacy of topical treatments is considered low rates of adherence to topical drugs. Patient support by the use of applications (apps) for smartphones is suggested to improve medical adherence.
METHODS/DESIGN: Design: An investigator-initiated, single-center, single-blind, parallel-group, phase-4 clinical superiority randomized controlled trial (RCT).
134 patients 18 to 75 years of age with mild-to-moderate psoriasis, who are capable of reading English language, own a smartphone, and are candidates for the study drug calcipotriol and betamethasone dipropionate (Cal/BD) cutaneous foam once daily prn (pro re nata).
A 28-day adherence-supporting app providing compulsory daily treatment reminders that pop-up on the smartphone screen with a short alert sound. The app synchronizes through Bluetooth® to an electronic monitor (EM) attached to the medication canister. The EM contains a chip registering the amount of foam, day and time the patient use the foam dispenser. The information is displayed in a diary that shows the amount of Cal/BD cutaneous foam used and the number of applied treatment sessions. The app has an optional diary with the patient's rating of symptoms. Non-intervention: Use of Cal/BD cutaneous foam and EM without the app. All participants are prescribed Cal/BD cutaneous foam prn for the entire study period. Primary outcome obtained in week 4: rates of adherence measured by patient report, weight of medication canisters, and number of treatment sessions measured by the EM. Secondary outcomes obtained at baseline, weeks 4, 8, and 26: Lattice System Physician's Global Assessment (LS-PGA) and Dermatology Quality of Life Index (DLQI).
This trial tests of whether an app can improve rates of adherence to a topical antipsoriatic drug. If the app improves rates of adherence and reduces the burden of psoriasis in a clinically significant way, the app could easily be implemented as a standard routine of care in the clinic.
NCT02858713 , registered on August 3, 2016. EudraCT number 2016-002143-42.
外用皮质类固醇或皮质类固醇/卡泊三醇制剂被推荐为银屑病的一线外用治疗方法,但外用治疗缺乏疗效的一个主要原因被认为是外用药物的依从率较低。建议通过使用智能手机应用程序(app)为患者提供支持,以提高医疗依从性。
方法/设计:设计:一项由研究者发起的、单中心、单盲、平行组、4期临床优效性随机对照试验(RCT)。
134名年龄在18至75岁之间、患有轻度至中度银屑病、能够阅读英语、拥有智能手机且适合使用研究药物卡泊三醇倍他米松二丙酸酯(Cal/BD)皮肤泡沫、按需每日一次(必要时)的患者。
一个为期28天的依从性支持应用程序,提供强制性的每日治疗提醒,会在智能手机屏幕上弹出并伴有简短的警报声。该应用程序通过蓝牙®与连接到药罐的电子监测器(EM)同步。电子监测器包含一个芯片,可记录泡沫的用量、患者使用泡沫分配器的日期和时间。这些信息显示在一个日记中,该日记显示了使用的Cal/BD皮肤泡沫的量以及应用治疗疗程的次数。该应用程序有一个供患者对症状进行评分的可选日记。非干预措施:使用Cal/BD皮肤泡沫和电子监测器,但不使用该应用程序。所有参与者在整个研究期间均按需开具Cal/BD皮肤泡沫。第4周获得的主要结局:通过患者报告、药罐重量以及电子监测器测量的治疗疗程次数来衡量的依从率。在基线、第4周、第8周和第26周获得的次要结局:格氏系统医生整体评估(LS-PGA)和皮肤病生活质量指数(DLQI)。
本试验测试一款应用程序是否能提高外用抗银屑病药物的依从率。如果该应用程序能提高依从率并以临床上显著的方式减轻银屑病负担,那么该应用程序可轻松作为临床标准常规护理措施实施。
NCT02858713,于2016年8月3日注册。欧洲临床试验数据库编号2016-002143-42。