一项针对成年癫痫患者数字自我管理干预的多中心随机对照可行性试验。

A multicenter randomized controlled feasibility trial of a digital self-management intervention for adults with epilepsy.

机构信息

Ruhr-Epileptology, Department of Neurology, University Hospital Knappschaftskrankenhaus Bochum, Ruhr University Bochum, Bochum, Germany.

Department of Neurology, Epilepsy Center Hessen, University Hospital and Philipps-University Marburg, Marburg, Germany.

出版信息

Epilepsia Open. 2024 Jun;9(3):1021-1033. doi: 10.1002/epi4.12933. Epub 2024 Apr 30.

Abstract

OBJECTIVE

Self-management interventions may enhance health-related quality of life (HRQoL) in epilepsy. However, several barriers often impair their implementation in the real world. Digital interventions may help to overcome some of these barriers. Considering this, the Helpilepsy Plus Prototype was developed as a prototype smartphone-delivered self-care treatment program for adults with epilepsy.

METHODS

The 12-week Helpilepsy Plus Prototype was evaluated through a randomized controlled feasibility trial with a waiting-list control (WLC) group. Outcome measurement at baseline and at 12 weeks assessed adherence to the prototype intervention and changes in epilepsy-related outcomes. The primary endpoint was patient autonomy measured with EASE, and secondary endpoints included HRQoL measured with QOLIE-31, health literacy measured with HLQ, anxiety, and depression symptoms measured with HADS. Semi-structured interviews were conducted with a heterogeneous sample of participants to assess user-friendliness and usefulness. The prototype program was delivered through the Neuroventis Platform (Neuroventis, BV, Overijse, Belgium), a certified medical device (under EU/MDD Class I, and EU/MDR grace period).

RESULTS

Ninety-two patients were included (46 in the intervention group, 46 in WLC). Most participants (63%, 58/92 women, median age 30 years) had pharmacoresistant epilepsy (61%, 56/92). Only 22% of participants (10/46) in the intervention group completed at least half of all intervention sessions. No significant differences between the intervention group and WLC were observed. Although there was a larger proportion of patients in the intervention group with meaningful improvements in HRQoL compared to WLC (19/46 versus 11/46), the difference was not significant (p = 0.119). Qualitative feedback showed that participants would appreciate more personalization, such as adaptation of the content to their current epilepsy knowledge level, a more interactive interface, shorter text sections, and interaction through reminders and notifications.

SIGNIFICANCE

Digital interventions should allow sufficient scope for personalization and interaction to increase patient engagement and enable benefits from self-care apps. Feedback loops allow the participatory development of tailored interventions.

PLAIN LANGUAGE SUMMARY

In this study, we investigated the effectiveness of an app-based self-help intervention. Study participants were either randomly assigned to a group that had access to the app or a group that received access to the app after the end of the study. Although a larger proportion of participants in the intervention group showed a relevant improvement in quality of life, the difference between the two groups was not statistically significant. Less than one-fifth of participants in the intervention group attended at least half of all intervention sessions; patient feedback showed that patients required more personalization and interactive options.

摘要

目的

自我管理干预措施可能会提高癫痫患者的健康相关生活质量(HRQoL)。然而,一些障碍常常会影响其在现实世界中的实施。数字干预措施可能有助于克服其中的一些障碍。考虑到这一点,开发了 Helpilepsy Plus 原型,作为一种用于癫痫成人的智能手机自我护理治疗程序的原型。

方法

通过一项随机对照可行性试验,对为期 12 周的 Helpilepsy Plus 原型进行了评估,该试验设有候补名单对照组(WLC)。在基线和 12 周时进行结果测量,以评估对原型干预的依从性和癫痫相关结果的变化。主要终点是通过 EASE 测量的患者自主性,次要终点包括通过 QOLIE-31 测量的 HRQoL、通过 HLQ 测量的健康素养、通过 HADS 测量的焦虑和抑郁症状。对一组不同的参与者进行了半结构化访谈,以评估用户友好性和有用性。该原型程序通过 Neuroventis 平台(Neuroventis,BV,Overijse,比利时)交付,这是一种经过认证的医疗设备(符合欧盟/MDD 一级标准,且处于欧盟/MDR 宽限期内)。

结果

共有 92 名患者入组(干预组 46 名,WLC 组 46 名)。大多数参与者(63%,58/92 名女性,中位年龄 30 岁)患有耐药性癫痫(61%,56/92)。只有 22%的干预组参与者(10/46)完成了所有干预课程的一半以上。干预组和 WLC 之间没有观察到显著差异。尽管干预组中有更多的患者在 HRQoL 方面有明显的改善(19/46 对 11/46),但差异无统计学意义(p=0.119)。定性反馈表明,参与者会更欣赏个性化,例如根据其当前的癫痫知识水平调整内容、更具交互性的界面、更短的文本部分以及通过提醒和通知进行交互。

意义

数字干预措施应允许足够的个性化和交互空间,以提高患者的参与度并使自我护理应用程序从中受益。反馈循环允许参与式开发定制干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae1/11145620/7051f05103a0/EPI4-9-1021-g001.jpg

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