- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving 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?
Studieoversikt
Status
Forhold
Detaljert beskrivelse
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.
Studietype
Registrering (Forventet)
Kontakter og plasseringer
Studiekontakt
- Navn: Chua Xin Hui
- Telefonnummer: +65-6601-1940
- E-post: xinhui.chua@nus.edu.sg
Studer Kontakt Backup
- Navn: Tay Zoey
- E-post: ephtz@nus.edu.sg
Studiesteder
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Singapore, Singapore, 117597
- Rekruttering
- Saw Swee Hock School of Public Health, National University of Singapore
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Ta kontakt med:
- Yeo Shumian
- Telefonnummer: +65-66013442
- E-post: yshumian@nus.edu.sg
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Prøvetakingsmetode
Studiepopulasjon
Beskrivelse
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.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Observasjonsmodeller: Kohort
- Tidsperspektiver: Potensielle
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
---|---|
Changes in health behaviours - physical activity
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: Baseline, 12 and 24 months follow up
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Baseline, 12 and 24 months follow up
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Sekundære resultatmål
Resultatmål |
Tidsramme |
---|---|
Blood pressure (mmHG)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: Baseline, 12 and 24 months follow-up
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Baseline, 12 and 24 months follow-up
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Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Falk Müller-Riemenschneider, National University, Singapore
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Forventet)
Studiet fullført (Forventet)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Andre studie-ID-numre
- Health@NUS
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
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Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
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