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

17 luglio 2026 aggiornato da: 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.

Panoramica dello studio

Descrizione dettagliata

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 di studio

Interventistico

Iscrizione (Stimato)

574

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

  • Nome: Levon Yongle Zhan, PhD
  • Numero di telefono: 852-25185656
  • Email: levon@hku.hk

Luoghi di studio

      • Hong Kong, Hong Kong
        • Reclutamento
        • District Health Centre/Expresses (DHC/E) in Yau Tsim Mong, Sha Tin and Kwai Tsing
        • Contatto:
          • Yongle Zhan, PhD
          • Numero di telefono: 852-25185656
          • Email: levon@hku.hk

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Prevenzione
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.
Comparatore attivo: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
Proportion of participants who sought medical assistance
Lasso di tempo: 3 months and 6 months
3 months and 6 months

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Proportion of healthy lifestyle behaviours
Lasso di tempo: 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
Lasso di tempo: 3 months and 6 months
3 months and 6 months
Level of satisfaction with the project
Lasso di tempo: 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

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Level of patient empowerment
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: William Chi Wai Wong, MD, The University of Hong Kong

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

1 giugno 2024

Completamento primario (Stimato)

30 settembre 2026

Completamento dello studio (Stimato)

31 marzo 2027

Date di iscrizione allo studio

Primo inviato

10 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

17 luglio 2026

Primo Inserito (Effettivo)

22 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

22 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

17 luglio 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su Cancro colorettale

Prove cliniche su Wellnuts app intervention

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