- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT05154227
Health@NUS - Studying Health Behaviours and Well-being During the Student-to-Work Life Transition Using mHealth
The study aims to investigate body-weight and behavioural trajectories, as well as their underlying individual, social, and environmental determinants from University to early working life. The study employs mHealth approaches in the form of a smartphone app and smart wearables to collect health behaviour and related information to answer the following research questions:
- To what extend do health behaviours (activity, diet, and sleep), body weight, and mental well-being change during the transition from university to early working life?
- What is the relationship between health behaviours and mental well-being, and how does it differ at different stages of the transition from University to early working life?
- What are the determinants of physical activity, healthy eating and sleep in university students and young working adults?
- Do these determinants differ at different stages of the student to work life transition?
- If so, how do these differences in these determinants relate to changes in health behaviours, weight status, and mental well-being?
Aperçu de l'étude
Statut
Les conditions
Description détaillée
This is a prospective cohort study. The study period for each participant is 2 years. Participants are required to download the study's smartphone app and wear the assigned smartwatch to collect various information (including step counts and sleep time). Physical measurements are taken in person at baseline, 12 months and 24 months visits. These measurements include height, weight, waist circumference, resting heart rate and blood pressure.
Questionnaires administered at baseline, 12 months and 24 months include:
- Demographics (age, gender, religion, socio-economic status, education level)
- Personality
- Dietary intake and habits
- Physical activity, sedentary behavior and screen time
- Active and passive transport use
- Smoking habit
- Sleep quality
- Mental health and wellness
- Medical history
- Women's health-related
Participants will also receive occasional surveys sent to their smartphone through the study app. These surveys will include questions about sleep, diet, technology use, binge drinking, smoking, physical activities and/or emotions.
Type d'étude
Inscription (Anticipé)
Contacts et emplacements
Coordonnées de l'étude
- Nom: Chua Xin Hui
- Numéro de téléphone: +65-6601-1940
- E-mail: xinhui.chua@nus.edu.sg
Sauvegarde des contacts de l'étude
- Nom: Tay Zoey
- E-mail: ephtz@nus.edu.sg
Lieux d'étude
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Singapore, Singapour, 117597
- Recrutement
- Saw Swee Hock School of Public Health, National University of Singapore
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Contact:
- Yeo Shumian
- Numéro de téléphone: +65-66013442
- E-mail: yshumian@nus.edu.sg
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
La description
Inclusion Criteria:
- Full time National University of Singapore students (undergraduate and postgraduate)
- Singapore Citizen or Permanent Resident;
- Has a Singapore registered mobile number• Owns a mobile phone with operating system that is compatible with the study app (iOS 10 or Android 7 and above);
- Able to make the upfront deposit of $20 and able to set up the Direct Debit Authorization (DDA) for possible deductions by HPB;
- Able to understand the study procedure during the informed consent taking process.
Exclusion Criteria:
- Students who will be overseas for more than 6 weeks per trip during the study period (e.g. involved in overseas exchange/internship programmes or stationed overseas) or travelling frequently;
- Students who are not able to set up the DDA via online method will be excluded;
- Students who has worked in a full-time position for more than a year previously;
- Pregnant women will be excluded only at the point of recruitment.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Modèles d'observation: Cohorte
- Perspectives temporelles: Éventuel
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
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Changes in health behaviours - physical activity
Délai: Baseline, 12 and 24 months follow up
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Baseline, 12 and 24 months follow up
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Changes in health behaviours - dietary pattern
Délai: Baseline, 12 and 24 months follow up
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Baseline, 12 and 24 months follow up
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Changes in health behaviours - sleep pattern
Délai: Baseline, 12 and 24 months follow up
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Baseline, 12 and 24 months follow up
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Changes in health behaviours - mental well-being
Délai: Baseline, 12 and 24 months follow up
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Baseline, 12 and 24 months follow up
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Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
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Blood pressure (mmHG)
Délai: Baseline, 12 and 24 months follow-up
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Baseline, 12 and 24 months follow-up
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Resting heart rate (bpm)
Délai: Baseline, 12 and 24 months follow-up
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Baseline, 12 and 24 months follow-up
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Body Mass Index (kg/m^2)
Délai: Baseline, 12 and 24 months follow-up
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Baseline, 12 and 24 months follow-up
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Waist circumference (cm)
Délai: Baseline, 12 and 24 months follow-up
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Baseline, 12 and 24 months follow-up
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Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Chercheur principal: Falk Müller-Riemenschneider, National University, Singapore
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Anticipé)
Achèvement de l'étude (Anticipé)
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
Autres numéros d'identification d'étude
- Health@NUS
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
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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 .