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Effectiveness of a Self-health Assessment Mobile Application in Young-to-midlife Adults in Hong Kong

17 de julho de 2026 atualizado por: William Chi Wai Wong, The University of Hong Kong

Effectiveness of Self-health Assessment Mobile Application to Promote Health Awareness, Empower Patients and Improve Linkage-to-care Amongst Young-to-midlife Adults in Hong Kong: a Randomised Controlled Trial

This project aims to compare the effectiveness of Wellnuts, an evidence-based, algorithm-driven self-health assessment mobile application, in empowering asymptomatic young-to-midlife adults in Hong Kong, promoting health awareness, and improving health-seeking behaviour and linkage-to-care, compared with conventional web-based health resources. Participants will be randomly allocated to the mobile health intervention group (Wellnuts app with self-health assessment and health information) and the conventional web-based resources control group (health information from Centre for Health Protection website). Hopefully, population health will be improved with the general health promotion impact from the app.

Visão geral do estudo

Descrição detalhada

The project is a mobile intervention that aims to promote health-seeking behaviour and linkage-to-care among asymptomatic young-to-midlife individuals in Hong Kong. In collaboration with The Lok Sin Tong Benevolent Society, Kowloon (LST), the app can be disseminated to large groups of people at relatively lower cost and address workforce and equity issues- accessing the difficult-to-reach groups. LST is a charitable organisation providing quality and diversified social, medical as well as educational services to the general population, especially for the underprivileged, with more than 50 multifunctional subsidiaries in Hong Kong. With promotion by LST, the app can outreach and benefit more people by offering more personalised and tailored advice compared to the conventional web-based resources.

Population health will be improved with the general health promotion impact from the app. Once this project validates the effectiveness of the app, and as the usage and availability of the app become more wide-reaching, it will benefit the general health of the local community in the long run. Increased awareness of common health conditions and associated modifiable behavioural risk factors will help reduce disease burden in the general community. Healthcare expenditure represents a massive social and financial burden for individuals and society. The creation of an algorithm-driven mobile app providing accurate and tailored health information to users regarding their personal risks through self-assessment components may generate interest from the community. This, in turn, would have a positive effect on modifiable behavioural risk factors awareness, promoting a personalised and modern solution to reducing healthcare burden.

This project will enhance our understanding of the challenges to behaviour modification of Hong Kong people. Through comprehensive surveys, we will be able to deepen our understanding of the challenges which make behavioral change difficult. The mobile app data and feedback from app users over time could inform policymakers and health services management on the facilitators and barriers to using mobile apps as an intervention and medium for health promotion. The findings will help the healthcare system keep up with the evolving demands and behaviors of patients in Hong Kong, as the region truly enters into the digital economy and age.

As mobile health intervention is a new and innovative approach, people may take some time to adopt it. However, previous research has reported the interests of people with different demographics in accessing health interventions on digital devices. Since mobile health interventions were user-friendly and effective at improving health outcomes, they can empower patients to seek help and improve linkage-to-care in order to address the ever-growing issue of chronic health conditions in Hong Kong.

In summary, mobile interventions are relatively new with mixed evidence for their effectiveness. Early studies based on specific groups, countries or diseases have shown promising results. Our study will be the first to examine a bilingual, technologically competent population in Hong Kong. The project is an eHealth intervention and could reach a large audience at a relatively low cost, which is not possible with traditional interventions delivered through centers or clinics.

Tipo de estudo

Intervencional

Inscrição (Estimado)

574

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

  • Nome: Levon Yongle Zhan, PhD
  • Número de telefone: 852-25185656
  • E-mail: levon@hku.hk

Locais de estudo

      • Hong Kong, Hong Kong
        • Recrutamento
        • District Health Centre/Expresses (DHC/E) in Yau Tsim Mong, Sha Tin and Kwai Tsing
        • Contato:
          • Yongle Zhan, PhD
          • Número de telefone: 852-25185656
          • E-mail: levon@hku.hk

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion Criteria:

  • Hong Kong residents self-reported age of 25-65 years;
  • Possesses a smartphone capable of running mobile apps (e.g. Android or iPhone) and;
  • Able to read either English or Chinese.

Exclusion Criteria:

  • Individuals having any symptoms or feeling unwell in anyways as detailed in the Disclaimer at the launch of the app; or
  • Individuals reporting a current diagnosis of cardiovascular disease, lung cancer, hepatitis B, colorectal cancer, diabetes, sexually transmitted diseases, depression, anxiety and mild cognitive impairment and memory loss.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Prevenção
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Intervention group
Participants allocated to the intervention group will use the Wellnuts mobile application.
The app adopts an evidence-based and algorithm-driven self-health assessment approach. It is designed to help participants assess their health risks, increase health awareness and encourage appropriate health-seeking behaviour. The app provides self-health assessment related to common health conditions and modifiable behavioural risk factors. Participants assessed as "at-risk" are provided with relevant recommendations, including recommended tests and follow-up actions where appropriate.
Comparador Ativo: Control group
Participants allocated to the control group will receive access to conventional web-based health resources from the Centre for Health Protection website which is run by the Department of Health.
Conventional web-based health resources are from the Centre for Health Protection website which was run by the Department of Health (https://www.chp.gov.hk/en/healthtopics/25/index.html). These resources provide general health information and links to relevant support groups.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Prazo
Proportion of participants who sought medical assistance
Prazo: 3 months and 6 months
3 months and 6 months

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Proportion of healthy lifestyle behaviours
Prazo: 3 months and 6 months
Lifestyle behaviours will be collected using a self-administered questionnaire. Healthy lifestyle behaviours include no tobacco smoking, no alcohol drinking, frequent physical activity, and diverse food intake.
3 months and 6 months
Proportion of participants who attended the follow-up tests after being assessed as "at risk" by the mobile app
Prazo: 3 months and 6 months
3 months and 6 months
Level of satisfaction with the project
Prazo: 3 months and 6 months
Level of satisfaction with the project will be evaluated using a five-point Likert item (very disappointed, disappointed, neutral, satisfied, very satisfied).
3 months and 6 months

Outras medidas de resultado

Medida de resultado
Descrição da medida
Prazo
Level of patient empowerment
Prazo: 6 months
Level of patient empowerment will be estimated using the Patient Enablement Instrument (PEI). PEI is a 6-item scale developed to assess the empowerment of patients after a consultation with their primary care clinician.
6 months

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Investigador principal: William Chi Wai Wong, MD, The University of Hong Kong

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

1 de junho de 2024

Conclusão Primária (Estimado)

30 de setembro de 2026

Conclusão do estudo (Estimado)

31 de março de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

10 de julho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

17 de julho de 2026

Primeira postagem (Real)

22 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

22 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

17 de julho de 2026

Última verificação

1 de julho de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Ensaios clínicos em Câncer colorretal

Ensaios clínicos em Wellnuts app intervention

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