Can an app supporting psoriasis patients improve adherence to topical treatment? A single-blind randomized controlled trial.

Q2 Medicine BMC Dermatology Pub Date : 2018-02-07 DOI:10.1186/s12895-018-0071-3
Mathias Tiedemann Svendsen, Flemming Andersen, Kirsten Hammond Andersen, Klaus Ejner Andersen
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引用次数: 12

Abstract

Background: 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).

Participants: 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).

Intervention: 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).

Discussion: 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.

Trial registration: NCT02858713 , registered on August 3, 2016. EudraCT number 2016-002143-42.

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支持牛皮癣患者的应用程序能提高局部治疗的依从性吗?一项单盲随机对照试验。
背景:外用皮质类固醇或皮质类固醇/钙化三醇制剂是银屑病推荐的一线外用治疗方法,但外用治疗缺乏疗效的主要原因是外用药物的依从率低。建议通过使用智能手机应用程序(app)来支持患者,以提高医疗依从性。方法/设计:设计:一项研究者发起、单中心、单盲、平行组、4期临床优势随机对照试验(RCT)。参与者:134名18至75岁的轻中度牛皮癣患者,能够阅读英语,拥有智能手机,并且是研究药物钙化三醇和二丙酸倍他米松(Cal/BD)皮肤泡沫的候选人,每天一次prn (pro re nata)。干预:一款为期28天的坚持支持应用程序,提供强制性的每日治疗提醒,它会在智能手机屏幕上弹出一个简短的提醒声音。该应用程序通过蓝牙®与附着在药罐上的电子监视器(EM)同步。EM包含一个芯片,记录泡沫的数量,患者使用泡沫分配器的日期和时间。该信息显示在日记中,显示Cal/BD皮肤泡沫的使用量和应用治疗疗程的次数。该应用程序有一个可选的日记,记录了患者的症状等级。非干预:在没有应用程序的情况下使用Cal/BD皮肤泡沫和EM。在整个研究期间,所有参与者都被规定使用Cal/BD皮肤泡沫。第4周获得的主要结果:患者报告测量的依从率、药物罐重量和EM测量的治疗次数。基线、第4周、第8周和第26周获得的次要结果:Lattice System医师整体评估(LS-PGA)和皮肤病生活质量指数(DLQI)。讨论:该试验测试应用程序是否可以提高局部抗银屑病药物的依从性。如果这款应用能在临床上显著提高患者的依从率,减轻牛皮癣患者的负担,那么这款应用就可以很容易地作为临床护理的标准常规实施。试验注册:NCT02858713, 2016年8月3日注册。草案编号2016-002143-42。
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BMC Dermatology
BMC Dermatology Medicine-Dermatology
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期刊介绍: BMC Dermatology is an open access journal publishing original peer-reviewed research articles in all aspects of the prevention, diagnosis and management of skin disorders, as well as related molecular genetics, pathophysiology, and epidemiology. BMC Dermatology (ISSN 1471-5945) is indexed/tracked/covered by PubMed, MEDLINE, CAS, EMBASE, Scopus and Google Scholar.
期刊最新文献
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