支持慢性疼痛患者的数字自我管理:可行性试点研究。
Digital Self-Management in Support of Patients Living With Chronic Pain: Feasibility Pilot Study.
作者信息
Bostrøm Katrine, Børøsund Elin, Varsi Cecilie, Eide Hilde, Flakk Nordang Elise, Schreurs Karlein Mg, Waxenberg Lori B, Weiss Karen E, Morrison Eleshia J, Cvancarova Småstuen Milada, Stubhaug Audun, Solberg Nes Lise
机构信息
Department of Digital Health Research, Division of Medicine, Oslo University Hospital, Oslo, Norway.
Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
出版信息
JMIR Form Res. 2020 Oct 23;4(10):e23893. doi: 10.2196/23893.
BACKGROUND
Chronic pain can be complex and taxing to live with, and treatment and support require a multicomponent approach, which may not always be offered or available. Smartphones, tablets, and personal computers are already incorporated into patients' daily lives, and therefore, they can be used to communicate, educate, and support self-management. Although some web-based self-management interventions exist, research examining the evidence and effect of digital solutions supporting self-management for patients living with chronic pain is limited, findings are inconclusive, and new innovative ideas and solutions are needed.
OBJECTIVE
This feasibility pilot study aimed to explore the system use, perceived usefulness, ease of use, and preliminary effects of EPIO, an app-based cognitive-behavioral pain self-management intervention program for patients living with chronic pain.
METHODS
The EPIO intervention was delivered in a blended-care model containing (1) one face-to-face introduction session, (2) nine cognitive behavior-based pain self-management modules, delivered in an app-based format for smartphones or tablets, and (3) one follow-up phone call at 2 to 3 weeks after the introduction session. Patients living with chronic pain (N=50) completed pre-post outcome measures at baseline and 3 months after the introduction session, with registration of system use (ie, log data) until 6 months. The use, perceived usefulness, and ease of use of the EPIO program were examined through system use data, as well as a study-specific use/usability questionnaire and the System Usability Scale (SUS). Outcome measures to test feasibility of use and estimate preliminary effects included the Brief Pain Inventory, health-related quality of life (HRQoL) scale, Hospital Anxiety and Depression Scale, Self-Regulatory Fatigue scale, Pain Catastrophizing Scale, and Chronic Pain Acceptance Questionnaire.
RESULTS
Participants (N=50) had a median age of 52 years (range 29-74 years) at inclusion and were mainly female (40/50, 80%). Thirty-one participants completed at least six of the nine modules within the 3-month study period (62% completion rate). Forty-five participants completed outcome measures at 3 months, and the EPIO program was rated as useful (ie, "totally agree" or "agree"; 39/45, 87%) and easy to use (42/45, 93%), and as having easily understandable exercises (44/45, 98%). The average overall system usability (SUS) score was 85.7, indicating grade A and excellent system usability. Preliminary psychosocial outcome measure estimates showed primarily nonsignificant pre-post intervention improvements at 3 months, but with significant positive effects related to some aspects of HRQoL (bodily pain, P=.02 and change, P=.049).
CONCLUSIONS
Digital self-management intervention programs may be of use and support for patients living with chronic pain. In this feasibility study, EPIO showed an acceptable program completion rate and was rated as useful and easy to use, with excellent user satisfaction. Program optimization and efficacy testing in a large-scale randomized controlled trial are warranted and in progress.
TRIAL REGISTRATION
ClinicalTrials.gov NCT03705104; https://clinicaltrials.gov/ct2/show/NCT03705104.
背景
慢性疼痛可能复杂且难以忍受,其治疗和支持需要多方面的方法,但这种方法可能并不总是能提供或可获得。智能手机、平板电脑和个人电脑已融入患者的日常生活,因此可用于沟通、教育和支持自我管理。尽管存在一些基于网络的自我管理干预措施,但针对支持慢性疼痛患者自我管理的数字解决方案的证据和效果的研究有限,结果尚无定论,需要新的创新理念和解决方案。
目的
本可行性试点研究旨在探索EPIO(一款针对慢性疼痛患者的基于应用程序的认知行为疼痛自我管理干预项目)的系统使用情况、感知有用性、易用性和初步效果。
方法
EPIO干预采用混合护理模式,包括(1)一次面对面介绍课程,(2)九个基于认知行为的疼痛自我管理模块,以基于应用程序的格式提供给智能手机或平板电脑,(3)在介绍课程后2至3周进行一次随访电话。慢性疼痛患者(N = 50)在基线和介绍课程后3个月完成前后结果测量,并记录系统使用情况(即日志数据)直至6个月。通过系统使用数据、特定研究的使用/可用性问卷和系统可用性量表(SUS)来检查EPIO项目的使用情况、感知有用性和易用性。用于测试使用可行性和估计初步效果的结果测量包括简明疼痛量表、健康相关生活质量(HRQoL)量表、医院焦虑抑郁量表、自我调节疲劳量表、疼痛灾难化量表和慢性疼痛接受问卷。
结果
参与者(N = 50)纳入时的中位年龄为52岁(范围29 - 74岁),主要为女性(40/50,80%)。31名参与者在3个月的研究期内完成了九个模块中的至少六个(完成率62%)。四十五名参与者在3个月时完成了结果测量,EPIO项目被评为有用(即“完全同意”或“同意”;39/45,87%)且易于使用(42/45,93%),并且练习易于理解(44/45,98%)。系统总体可用性(SUS)的平均得分为85.7,表明为A级且系统可用性极佳。初步的心理社会结果测量估计显示,在3个月时干预前后的改善主要无统计学意义,但与HRQoL的某些方面有显著的积极影响(身体疼痛,P = 0.02;变化,P = 0.049)。
结论
数字自我管理干预项目可能对慢性疼痛患者有用并提供支持。在本可行性研究中,EPIO显示出可接受的项目完成率,被评为有用且易于使用,用户满意度极高。在大规模随机对照试验中进行项目优化和疗效测试是必要的且正在进行中。
试验注册
ClinicalTrials.gov NCT03705104;https://clinicaltrials.gov/ct2/show/NCT03705104