Views, barriers, and facilitators of people living with human immunodeficiency virus and healthcare professionals regarding the use of a mobile health application to improve HIV self-care in Malaysia
Clinical Snapshot
PICO Framework
| P — Population | People living with HIV (n=17) and healthcare professionals (doctors n=9, nurses n=2) in Malaysia who owned smartphones and understood English or Malay |
| I — Intervention | Mobile health application (m-HA) for HIV self-care |
| C — Comparator | Not applicable - qualitative exploration of views and experiences |
| O — Outcomes | Views, barriers, and facilitators regarding m-HA use; perceived benefits, concerns, motivators, and influences |
Bottom Line
This Malaysian qualitative study explored stakeholder views on mobile health applications for HIV self-care among 17 people living with HIV and 11 healthcare professionals. Three key themes emerged: participants saw potential benefits for knowledge improvement and healthcare access but expressed concerns about information overload and data security; high utilitarian and hedonic motivators were perceived to drive usage; and peer or healthcare professional endorsement was viewed as crucial for adoption. The study provides valuable insights for developing patient-centred mobile health solutions in HIV care, though findings are limited by single-site recruitment and unclear ethical reporting. The research addresses an important gap in understanding stakeholder perspectives on digital health interventions for chronic disease self-management, with implications for similar healthcare settings globally.
Key Findings
P Value: Not applicable - qualitative study
Effect Size: Not applicable - qualitative study
Primary Outcome: Three main themes: (1) Perceived benefits and concerns regarding m-HA usage, (2) Perceived motivators of m-HA, (3) Perceived influences to use m-HA
Nnt Or Sensitivity: Not applicable - qualitative study exploring perceptions and experiences
Confidence Interval: Not applicable - qualitative study
Clinical Application
Findings suggest feasibility dependent on addressing data security concerns, preventing information overload, and ensuring peer/HCP endorsement for uptake Relevant to Australian HIV care given similar smartphone penetration and digital health initiatives, though cultural adaptation needed for Indigenous and CALD communities. Could inform PBS-funded digital health interventions and align with National Digital Health Strategy People living with HIV in resource-appropriate settings with smartphone access, particularly relevant to Malaysian and similar Southeast Asian healthcare contexts
Abstract
AIM: The views, barriers, and facilitators of people living with HIV (PLWH) and healthcare professionals (HCPs), regarding the use of a mobile health application (m-HA) to improve HIV self-care were explored. SUBJECT AND METHODS: Seventeen PLWH, nine doctors and two nurses who owned a smartphone and understood English or Malay were recruited from the infectious disease clinic of a tertiary hospital in Malaysia. Semi-structured in-depth interviews were conducted face-to-face using a topic guide, audio-recorded and transcribed verbatim. Data was analysed using reflexive thematic analysis. Two researchers independently coded transcripts and met to resolve discrepancies and develop themes. Data collection continued until thematic saturation was achieved. RESULTS: Three themes emerged: (1) Perceived benefits and concerns regarding m-HA usage: participants perceived m-HA could improve knowledge, but expressed concerns regarding information overload. Participants viewed m-HA as a means to enhance access to hospital services like clinic visits, medication refills, communication with HCPs, and medical records documentation. However, concerns regarding misuse, data confidentiality and security remained. (2) Perceived motivators of m-HA: participants perceived that high utilitarian and hedonic motivators increase m-HA usage. (3) Perceived influences to use m-HA: participants believed PLWH would use m-HA if introduced by their peers or HCPs. CONCLUSION: These findings provided information for developing a patient-centred m-HA to improve HIV self-care in Malaysia.
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