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

Author:

Ng Wei Leik1ORCID,Ng Chirk Jenn123ORCID,Teo Chin Hai14,Ang Tan Fong5,Lee Yew Kong14,Abdul Hadi Haireen1,Chiang De Min1ORCID,Mohd Noor Mohd Khairi6,Syed Omar Sharifah Faridah7,Ong Hang Cheng7,Wong Pui Li7,Kukreja Anjanna7,Chiew Thiam Kian8,Ong Sim Ying8,Noor Azhar Abdul Muhaimin9

Affiliation:

1. Department of Primary Care Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Wilayah Persekutuan, Malaysia

2. Department of Research, SingHealth Polyclinics, Singapore, Singapore

3. Health Services and Systems Research, Duke-NUS Medical School, Singapore, Singapore

4. UM eHealth Unit, Faculty of Medicine, University of Malaya, Kuala Lumpur, Wilayah Persekutuan, Malaysia

5. Department of Computer System and Technology, Faculty of Computer Science and Information Technology, University of Malaya, Kuala Lumpur, Wilayah Persekutuan, Malaysia

6. Shah Alam Section 7 Health Clinic, Ministry of Health Malaysia, Selangor, Malaysia

7. Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia

8. Department of Software Engineering, Faculty of Computer Science and Information Technology, University of Malaya, Kuala Lumpur, Malaysia

9. Department of Emergency Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia

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.

Funder

University of Malaya Impact-Oriented Interdisciplinary Research Grant Programme

Publisher

SAGE Publications

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