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SMArT Work: Stand More AT Work

Effectiveness of a behaviour-change intervention with sit-stand desks on NHS desk-based staff’s sitting time and associated factors (SMArT Work): a cluster randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN10967042
Enrollment
136
Registered
2015-02-02
Start date
2015-10-31
Completion date
Unknown
Last updated
2020-10-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sedentary behaviour and associated conditions (e.g., musculoskeletal health) Injury, Occupational Diseases, Poisoning Occupational health

Interventions

1. A cluster randomised controlled trial will be undertaken at three University Hospitals of Leicester (UK
Leicester General Hospital, Leicester Royal Infirmary and Glenfield General Hospital), with the unit of randomisation being at the level of each self-contained building or block. 2. Th
control sites will have limited opportunity to substantially increase their standing activity during working hours

Sponsors

Loughborough University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Health professionals 2. Healthy volunteers 3. Age 18–70 years old 4. Able to speak and read English 5. Willing and able to give full informed consent for themselves 6. NHS-office based, predominantly sedentary staff employed by the University Hospitals of Leicester NHS Trust

Exclusion criteria

Exclusion criteria: 1. Younger than 18 years old or older than 70 years old 2. Unable to give informed consent 3. NHS staff not predominantly in office-based jobs

Design outcomes

Primary

MeasureTime frame
Long-term (12 months) changes: objectively measured sedentary behaviour at baseline, 3 months, 6 months, and 12 months using self-monitoring devices (including LumoBack, GeneActive and ActivPAL) worn by participants

Secondary

MeasureTime frame
1. Change in sedentary behaviour over the short term (3 months and 6 months) measured objectively 2. Absenteeism (using employment records) 3. Job performance 4. Job satisfaction 5. Work engagement 6. Occupational fatigue 7. Musculoskeletal health 8. Mood/affective states 9. Quality of life (self assessment) 10. Cognitive ability (using experimental measures such as the Hopkins Verbal Learning Test, the Digit-Symbol Subsitition Test, and Stroop Test) Secondary outcomes will be measured at baseline, 3 months, 6 months, and 12 months after the intervention using a range of validated psychometric measures (occupational fatigue, musculoskeletal health, mood/affective states and quality of life), self-report (job performance, job satisfaction and work engagement), employer records (absenteeism) and experimental cognitive tasks (cognitive ability).

Countries

United Kingdom

Contacts

Public ContactFehmidah;Sophie Munir;O'Connell

;

f.munir@lboro.ac.uk;sophie.oconnell@uhl-tr.nhs.uk+44 (0)1509 228 228;+44 (0)116 258 8571

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 3, 2026