- ICH GCP
- US Clinical Trials Registry
- Clinical Trial 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?
Study Overview
Status
Conditions
Detailed Description
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.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Chua Xin Hui
- Phone Number: +65-6601-1940
- Email: xinhui.chua@nus.edu.sg
Study Contact Backup
- Name: Tay Zoey
- Email: ephtz@nus.edu.sg
Study Locations
-
-
-
Singapore, Singapore, 117597
- Recruiting
- Saw Swee Hock School of Public Health, National University of Singapore
-
Contact:
- Yeo Shumian
- Phone Number: +65-66013442
- Email: yshumian@nus.edu.sg
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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.
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Changes in health behaviours - physical activity
Time Frame: Baseline, 12 and 24 months follow up
|
Baseline, 12 and 24 months follow up
|
Changes in health behaviours - dietary pattern
Time Frame: Baseline, 12 and 24 months follow up
|
Baseline, 12 and 24 months follow up
|
Changes in health behaviours - sleep pattern
Time Frame: Baseline, 12 and 24 months follow up
|
Baseline, 12 and 24 months follow up
|
Changes in health behaviours - mental well-being
Time Frame: Baseline, 12 and 24 months follow up
|
Baseline, 12 and 24 months follow up
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Blood pressure (mmHG)
Time Frame: Baseline, 12 and 24 months follow-up
|
Baseline, 12 and 24 months follow-up
|
Resting heart rate (bpm)
Time Frame: Baseline, 12 and 24 months follow-up
|
Baseline, 12 and 24 months follow-up
|
Body Mass Index (kg/m^2)
Time Frame: Baseline, 12 and 24 months follow-up
|
Baseline, 12 and 24 months follow-up
|
Waist circumference (cm)
Time Frame: Baseline, 12 and 24 months follow-up
|
Baseline, 12 and 24 months follow-up
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Falk Müller-Riemenschneider, National University, Singapore
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Health@NUS
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Healthy
-
Prevent Age Resort "Pervaya Liniya"RecruitingHealthy Aging | Healthy Diet | Healthy LifestyleRussian Federation
-
Maastricht University Medical CenterCompletedHealthy Volunteers | Healthy Subjects | Healthy AdultsNetherlands
-
Yale UniversityNot yet recruitingHealth-related Benefits of Introducing Table Olives Into the Diet of Young Adults: Olives For HealthHealthy Diet | Healthy Lifestyle | Healthy Nutrition | CholesterolUnited States
-
University of PennsylvaniaActive, not recruitingHealthy | Healthy AgingUnited States
-
Chalmers University of TechnologyGöteborg UniversityCompletedHealthy | Nutrition, HealthySweden
-
Hasselt UniversityRecruitingHealthy | Healthy AgingBelgium
-
Galera Therapeutics, Inc.Syneos HealthCompleted
-
Galera Therapeutics, Inc.Syneos HealthCompletedHealthy | Healthy VolunteersAustralia
-
University of ManitobaNot yet recruitingHealthy | Healthy Diet