NCT07887269

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,000

participants targeted

Target at P75+ for not_applicable

Timeline
35mo left

Started Sep 2026

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress5%
Sep 2026Sep 2029

Study Start

First participant enrolled

September 1, 2026

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

October 7, 2026

Completed
14 days until next milestone

First Posted

Study publicly available on registry

October 21, 2026

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2029

Expected
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2029

Last Updated

October 21, 2026

Status Verified

October 1, 2026

Enrollment Period

2.3 years

First QC Date

October 7, 2026

Last Update Submit

October 14, 2026

Conditions

Keywords

SedentarinessPhysical ActivitySleepWorkplace Intervention

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

EXPERIMENTAL

The 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.

Behavioral: NUS Health Prog

Interventions

NUS Health ProgBEHAVIORAL

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.

Intervention

Eligibility Criteria

Age21 Years - 70 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

RECRUITING

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

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Model Details: The 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.
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

Locations