Sleep Health, Workplace Stress and Wellbeing in NUS Staff: the NUS1000 Staff Edition Study
NUS1000SE
1 other identifier
observational
1,000
1 country
1
Brief Summary
Workplace stress can significantly affect workers sleep, physical health and mental wellbeing. Recognizing and characterizing obstacles to healthy sleep patterns in office workers can help identify targets for corporate interventions that improve productivity and workplace wellbeing. Following the investigator\'s experience with the NUS1000 study in 1st year students conducted in Aug-Dec 2023, the investigators will now track daily sleep, wellbeing and time-use in NUS staff for 1 year in the present study. These data will reveal work-related stressors that impact daily sleep and mood. In addition, the investigators will investigate whether daily sleep and stress are associated with cardiovascular health in this middle-age cohort.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Nov 2024
Shorter than P25 for all trials
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
First Submitted
Initial submission to the registry
September 3, 2024
CompletedFirst Posted
Study publicly available on registry
September 19, 2024
CompletedStudy Start
First participant enrolled
November 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2025
CompletedSeptember 19, 2024
September 1, 2024
1 year
September 3, 2024
September 10, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (13)
Time-use diary
Participants will be asked to fill out a time-use diary over 2-week periods every 3 months throughout the follow-up period (Month 1, Month 3, Month 6, Month 9 and Month 12), indicating the activities they engaged in over the past day on the smartphone app.
Across the 1 year study
Blood Pressure
Blood pressure measures will be taken twice via an Omron blood pressure device.
Across the 1 year study
Arterial Stiffness
Arterial stiffness will be assessed by SphygmoCor XCEL system (cuff plus tonometer) and pulse wave velocity will be derived.
Across the 1 year study
Height
Height will be measured by the device linked to the body composition system (cm).
Across the 1 year study
Weight
Weight will be measured by the device linked to the body composition system (in kg).
Across the 1 year study
Body composition
Body composition will be assessed by InBody 770 Bioelectrical Impedance Analysis machine.
Across the 1 year study
Smartphone Touchscreen Interactions
Smartphone taps (number) will be tracked automatically through an EU-GDPR (the European Union's stringent privacy regulation) compliant smartphone app (QuantActions). This application logs human-smartphone screen interactions (e.g., taps, swipes) during regular use by logging a location-specific timestamp for each screen contact, and the name of the active app at that moment. This gives us a readout of phone use, app use, and an implicit measure of alertness (tapping speed). Only timestamps of touchscreen interactions and the associated apps will be recorded. No text, pictures, contacts, or any person identifying information will be collected. Moreover, data will be gathered and stored on the cloud using codes only; names or emails will not be collected.
Across the 1 year study
Sleep time
The Oura ring is a device worn on the finger which non-invasively records movement, heart rate and temperature to infer sleep and physical activity. Sleep Onset Time, Wake Time, on Workday (weekday) and Free Day (Weekend / vacation) will be recorded for nocturnal sleep and naps.
Across the 1 year study
Sleep duration
The Oura ring is a device worn on the finger which non-invasively records movement, heart rate and temperature to infer sleep and physical activity. Sleep Duration on Workday (weekday) and Free Day (Weekend / vacation) will be recorded for nocturnal sleep and naps.
Across the 1 year study
Wake after sleep onset
The Oura ring is a device worn on the finger which non-invasively records movement, heart rate and temperature to infer sleep and physical activity. Wake after Sleep Onset on Workday (weekday) and Free Day (Weekend / vacation) will be recorded.
Across the 1 year study
Sleep regularity
The Oura ring is a device worn on the finger which non-invasively records movement, heart rate and temperature to infer sleep and physical activity. Sleep Regularity (computed via Std Deviation and Sleep Regularity Index; evaluated over 4 weeks minimally) will be recorded.
Across the 1 year study
Well-being
Participants input ratings about a rotating set of questions concerning wellbeing daily through a smartphone based app (Z4IP) that has been used in prior studies. This daily assessment can be done anytime between 8pm and 12am each day. Higher scores represent higher levels of well-being.
Across the 1 year study
Self-reported health
Participants will also be required to complete a subset of health questionnaires every 3 months throughout the follow-up period (Month 1, Month 3,Month 6, Month 9 and Month 12) on the Qualtrics survey platform.
Across the 1 year study
Study Arms (1)
Staff
NUS Staff
Eligibility Criteria
1000 National University of Singapore staff
You may qualify if:
- NUS staff between the age of 35-70 with smartphones operating on Android 8.0 and up, or iOS 14.0 or later
You may not qualify if:
- Participants will be required to :
- Have their sleep and physical activity rhythms recorded via wearable sensors, while they continue daily life as usual.
- Complete periodic questionnaires and short daily surveys on their smartphones.
- Agree to interactions with their smartphones and NUS e-services (e.g., email) tracked.
- Participants who do not agree to have these measures recorded will not be eligible for the study. Shift workers (e.g., security personnel, doctors and nurses), nursing/pregnant woman, and patients with existing sleep/psychological disorders (e.g., insomnia and major depression) will also be excluded.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Yong Loo Lin School of Medicine
Singapore, Singapore, 117549, Singapore
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
September 3, 2024
First Posted
September 19, 2024
Study Start
November 1, 2024
Primary Completion
November 1, 2025
Study Completion
November 1, 2025
Last Updated
September 19, 2024
Record last verified: 2024-09
Data Sharing
- IPD Sharing
- Will not share