Feasibility and acceptability of a dengue self-monitoring system to reduce treatment delay in Malaysia: A single-centre pilot randomised controlled trial.

IF 2.9 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES DIGITAL HEALTH Pub Date : 2024-09-05 eCollection Date: 2024-01-01 DOI:10.1177/20552076241277710
Wei Leik Ng, Chirk Jenn Ng, Chin Hai Teo, Tan Fong Ang, Yew Kong Lee, Haireen Abdul Hadi, De Min Chiang, Mohd Khairi Mohd Noor, Sharifah Faridah Syed Omar, Hang Cheng Ong, Pui Li Wong, Anjanna Kukreja, Thiam Kian Chiew, Sim Ying Ong, Abdul Muhaimin Noor Azhar
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Abstract

Objective: Most dengue cases are managed in an outpatient setting, where patients are advised to return to the clinic daily for monitoring. Some patients can develop severe dengue at home and fail to recognise the deterioration. An application called DengueAid was designed as a self-monitoring tool for patients to reduce delay in seeking timely treatment. This study aimed to assess the feasibility of conducting a randomised controlled trial to determine the effectiveness of the DengueAid application.

Methods: Dengue patients were recruited from a public health clinic in Malaysia and randomised to either use the DengueAid application plus standard care for dengue or receive only the standard care. The outcomes evaluated were the (1) feasibility of recruitment, data collection and follow-up procedures; (2) preliminary clinical outcome measures; and (3) acceptability of DengueAid. Qualitative interviews were conducted for participants in the intervention arm to assess the acceptability of DengueAid.

Results: Thirty-seven patients were recruited with 97% (n = 36) retention rates. The recruitment rate was low (63% refusal rate, n = 62/99) with difficulty in data collection and follow-up due to the variable interval of care for dengue in an outpatient setting. DengueAid application was acceptable to the participants, but preliminary clinical outcomes and qualitative data suggested limited utility of the application. Unwell conditions of patients and limited access to healthcare are important factors impacting the application's utility.

Conclusion: The feasibility trial uncovered issues with recruitment, data collection and follow-up processes. Further research and modification to the application are needed to improve its utility and usability.

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马来西亚登革热自我监测系统减少治疗延误的可行性和可接受性:单中心试点随机对照试验。
目的:大多数登革热病例都是在门诊治疗的,医生建议病人每天回诊所接受监测。有些患者可能在家中患上严重登革热,却无法察觉病情的恶化。我们设计了一款名为 "登革热援助"(DengueAid)的应用程序,作为患者的自我监测工具,以减少延误及时治疗的情况。本研究旨在评估开展随机对照试验的可行性,以确定 DengueAid 应用程序的有效性:方法:从马来西亚的一家公共卫生诊所招募登革热患者,并随机分配他们使用 DengueAid 应用程序和标准登革热治疗方法,或仅接受标准治疗方法。评估结果包括:(1) 招募、数据收集和随访程序的可行性;(2) 初步临床结果测量;(3) DengueAid 的可接受性。对干预组的参与者进行了定性访谈,以评估 DengueAid 的可接受性:招募了 37 名患者,保留率为 97%(n = 36)。招募率较低(拒绝率为 63%,n = 62/99),由于门诊登革热治疗的间隔时间不固定,因此在数据收集和随访方面存在困难。参与者可以接受登革热援助应用程序,但初步临床结果和定性数据表明该应用程序的实用性有限。患者的身体状况不佳和获得医疗服务的途径有限是影响该应用实用性的重要因素:可行性试验发现了招募、数据收集和跟踪过程中存在的问题。需要对该应用程序进行进一步研究和修改,以提高其实用性和可用性。
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
DIGITAL HEALTH
DIGITAL HEALTH Multiple-
CiteScore
2.90
自引率
7.70%
发文量
302
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