Health@NUS - Studying Health Behaviours and Well-being During the Student-to-Work Life Transition Using mHealth

November 30, 2021 updated by: Dr Falk Mueller-Riemenschneider, National University, Singapore

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:

  1. 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?
  2. 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?
  3. What are the determinants of physical activity, healthy eating and sleep in university students and young working adults?
  4. Do these determinants differ at different stages of the student to work life transition?
  5. If so, how do these differences in these determinants relate to changes in health behaviours, weight status, and mental well-being?

Study Overview

Status

Recruiting

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

Observational

Enrollment (Anticipated)

1300

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Singapore, Singapore, 117597
        • Recruiting
        • Saw Swee Hock School of Public Health, National University of Singapore
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 26 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

This is a cohort of National University of Singapore (NUS) (undergraduate and postgraduate) students.

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Falk Müller-Riemenschneider, National University, Singapore

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 20, 2020

Primary Completion (Anticipated)

November 1, 2023

Study Completion (Anticipated)

November 1, 2023

Study Registration Dates

First Submitted

September 16, 2021

First Submitted That Met QC Criteria

November 30, 2021

First Posted (Actual)

December 13, 2021

Study Record Updates

Last Update Posted (Actual)

December 13, 2021

Last Update Submitted That Met QC Criteria

November 30, 2021

Last Verified

November 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • Health@NUS

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

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