- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07720245
Effectiveness of a Self-health Assessment Mobile Application in Young-to-midlife Adults in 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
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
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.
Type d'étude
Inscription (Estimé)
Phase
- N'est pas applicable
Contacts et emplacements
Coordonnées de l'étude
- Nom: Levon Yongle Zhan, PhD
- Numéro de téléphone: 852-25185656
- E-mail: levon@hku.hk
Lieux d'étude
-
-
-
Hong Kong, Hong Kong
- Recrutement
- District Health Centre/Expresses (DHC/E) in Yau Tsim Mong, Sha Tin and Kwai Tsing
-
Contact:
- Yongle Zhan, PhD
- Numéro de téléphone: 852-25185656
- E-mail: levon@hku.hk
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
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.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: La prévention
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 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.
|
|
Comparateur actif: 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.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
Proportion of participants who sought medical assistance
Délai: 3 months and 6 months
|
3 months and 6 months
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Proportion of healthy lifestyle behaviours
Délai: 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
Délai: 3 months and 6 months
|
3 months and 6 months
|
|
|
Level of satisfaction with the project
Délai: 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
|
Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Level of patient empowerment
Délai: 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
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: William Chi Wai Wong, MD, The University of Hong Kong
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Processus pathologiques
- Tumeurs par site
- Tumeurs
- Attributs de la maladie
- Maladies intestinales
- Maladies des voies respiratoires
- Tumeurs gastro-intestinales
- Tumeurs du système digestif
- Maladies du système digestif
- Maladies gastro-intestinales
- Tumeurs intestinales
- Maladies rectales
- Maladies pulmonaires
- Tumeurs des voies respiratoires
- Tumeurs thoraciques
- Maladies du côlon
- Conditions pathologiques, signes et symptômes
- Tumeurs pulmonaires
- Tumeurs colorectales
- Maladie chronique
Autres numéros d'identification d'étude
- 07220148 (Autre subvention/numéro de financement: Health and Medical Research Fund)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .