NUS Health Study: Improving Sleep, Sedentariness and Physical Activity in NUS Staff
NUS Health
1 other identifier
interventional
2,000
1 country
1
Brief Summary
'NUS Health' is a workplace-embedded health program for National University of Singapore (NUS) staff that concurrently targets sleep, sedentary behaviour, and physical activity. The intervention adopts a multilevel socioecological approach, integrating individual, social, environmental, and organisational strategies to support sustainable behaviour change. The study team will evaluate the feasibility, acceptability, and effectiveness of this program in improving sleep and movement behaviours, with anticipated downstream benefits for cardiometabolic health, psychological well-being, and workplace productivity. Findings from this study will inform the development of future institution-wide health initiatives and contribute to the evidence base for integrated workplace interventions targeting multiple lifestyle risk factors simultaneously.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2026
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2026
CompletedFirst Submitted
Initial submission to the registry
October 7, 2026
CompletedFirst Posted
Study publicly available on registry
October 21, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2029
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 1, 2029
October 21, 2026
October 1, 2026
2.3 years
October 7, 2026
October 14, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (13)
Sendentariness, via OURA ring
Amount of sedentary time daily, as measured by the OURA ring's sedentariness metric (energy expenditure of 1.5 metabolic equivalents (METs) or less ).
Through study completion, daily, an average of 2 years
Moderate-to-vigorous activity (MVPA), via OURA ring
Amount of daily moderate-to-vigorous activity (MVPA), as measured by the OURA ring.
Through study completion, daily, an average of 2 years
Light-intensity physical activity (LPA), via OURA ring
Amount of daily light-intensity physical activity (LPA), as measured by the OURA ring.
Through study completion, daily, an average of 2 years
Sleep duration, via OURA ring
Sleep duration as measured by the OURA ring.
Through study completion, daily, an average of 2 years
Sleep duration variability
The dispersion of daily sleep duration values around a participant's personal average.
Through study completion, an average of 2 years
Sleep onset time, via OURA ring
Sleep onset time as measured by the OURA ring.
Through study completion, daily, an average of 2 years
Sleep onset variability
The dispersion of daily sleep onset timing values around a participant's personal average.
Through study completion, an average of 2 years
Glucose trends across 2 weeks
Measured via Continuous Glucose Monitor
2 weeks measurement period at baseline; subsequently at 9 months, and 15 months after baseline measurement
Full blood count
Measured via venous blood collection
At baseline; subsequently 9 months, and 15 months after baseline measurement
Liver panel
Measured via venous blood collection
At baseline; subsequently at 9 months, and 15 months after baseline measurement
Renal panel
Measured via venous blood collection
At baseline; subsequently at 9 months, and 15 months after baseline measurement
Iron studies
Measured via venous blood collection
At baseline; subsequently at 9 months, and 15 months after baseline measurement
Urine panel
Measured via urine collection
At baseline; subsequently at 9 months, and 15 months after baseline measurement
Study Arms (1)
Intervention
EXPERIMENTALThe intervention involves the concurrent implementation of strategies to optimize sleep, reduce sedentary behaviour, and enhance incidental physical activity through an workplace embedded health promotion program. Participants will receive personalised goals and feedback based on their wearable-derived biometric data. An incentive system will be used to encourage engagement with the intervention and study procedures.
Interventions
For the sleep component, personalised goals will focus on reducing or maintaining a low frequency of short sleep nights and, where appropriate, advancing sleep timing among individuals with delayed sleep schedules. Goals will be tailored to each participant using their biometric data. For the sedentariness component, personalised goals will focus on reducing daily sedentary time, with an overall target of approximately 8 hours per day or less. For the physical activity component, personalised goals will focus on increasing or maintaining moderate-to-vigorous physical activity (MVPA) levels.
Eligibility Criteria
You may qualify if:
- Full time NUS staff
- Willing to undergo blood draw procedure
You may not qualify if:
- Staff who tender their resignation from NUS during the 16-month study period will be discontinued from the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National University of Singapore
Singapore, 117549, Singapore
Related Publications (1)
Pereira MA, Mullane SL, Toledo MJL, Larouche ML, Rydell SA, Vuong B, Feltes LH, Mitchell NR, de Brito JN, Hasanaj K, Carlson NG, Gaesser GA, Crespo NC, Oakes JM, Buman MP. Efficacy of the 'Stand and Move at Work' multicomponent workplace intervention to reduce sedentary time and improve cardiometabolic risk: a group randomized clinical trial. Int J Behav Nutr Phys Act. 2020 Oct 27;17(1):133. doi: 10.1186/s12966-020-01033-3.
PMID: 33109190BACKGROUND
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor Michael Chee Wei Liang
Study Record Dates
First Submitted
October 7, 2026
First Posted
October 21, 2026
Study Start
September 1, 2026
Primary Completion (Estimated)
January 1, 2029
Study Completion (Estimated)
September 1, 2029
Last Updated
October 21, 2026
Record last verified: 2026-10
Data Sharing
- IPD Sharing
- Will not share