- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02932787
Effects of Installing Height-adjustable Workstations on Office Workers Workplace Sitting Time and Productivity
Effects of Installing Height-adjustable Workstations on Occupational Sitting Time and Workplace Productivity in Desk-based Workers
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Sedentary behaviour has been found to be ubiquitous within the workplace and due to the negative consequences of sedentary behaviour upon health, research has began to look at ways to reduce and interrupt sedentary behaviour.
Interventions that have introduced height-adjustable workstations into the workplace have been found to reduce sedentary behaviour. Some employees and employers are concerned that using height-adjustable workstations and trying to reduce workplace sedentary behaviour can lead to a loss of workplace productivity.
The present study looked at the effects of installing height-adjustable workstations on occupational sitting time and workplace productivity in desk-based workers. Workplace activity was measured objectively using ActivPal accelerometers and productivity was measured via self-report measures. Measurements took place at baseline and four weeks after receiving the height-adjustable workstation.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- age 18 to 65 years,
- working ≥0.6 full time equivalents,
- access to a work telephone and desktop computer with internet,
- not pregnant,
- no planned absence >1 week during the trial,
- not chair-bound or uniquely impaired such that reducing occupational sitting time was not feasible,
- no pre-existing musculoskeletal disorder.
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control
|
|
Experimental: Height-adjustable workstation
Participants received a height-adjustable workstation for four weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in Workplace Sedentary Time
Time Frame: Baseline (0 weeks), 4 weeks after installation of height-adjustable workstations
|
The amount of time a participant spends sitting whilst in the workplace (minutes).
This was measured using a thigh-worn ActivPAL accelerometer.
|
Baseline (0 weeks), 4 weeks after installation of height-adjustable workstations
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in Workplace Absenteeism Using the World Health Organisation Health and Work Performance Questionnaire
Time Frame: Baseline (0 weeks), 4 weeks after installation of height-adjustable workstations
|
Self-reported absolute absenteeism (the amount of time a participant was absent from work for during the previous 7-days) measured using the World Health Organisation Health and Work Performance Questionnaire.
This is calculated in relation to a participants contracted hours, therefore a negative score shows that a participant worked less than they are contracted to, where as a positive score means a participant reported working more hours than they are contracted to.
|
Baseline (0 weeks), 4 weeks after installation of height-adjustable workstations
|
Change in Workplace Presenteeism Using the World Health Organisation Health and Work Performance Questionnaire
Time Frame: Baseline (0 weeks), 4 weeks after installation of height-adjustable workstations
|
Self-reported absolute presenteeism (an employees productivity during working hours) measured using the World Health Organisation Health and Work Performance Questionnaire.
The higher the percentage, the more productive a participant felt they were.
100% means that they felt they were productive the whole time they were working.
Presenteeism can be impacted upon by illness and other health conditions, if a person was feeling ill or had a back problem, this may mean that they are less productive whilst at work.
|
Baseline (0 weeks), 4 weeks after installation of height-adjustable workstations
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Simon H Till, Sheffield Hallam University
Publications and helpful links
General Publications
- Neuhaus M, Eakin EG, Straker L, Owen N, Dunstan DW, Reid N, Healy GN. Reducing occupational sedentary time: a systematic review and meta-analysis of evidence on activity-permissive workstations. Obes Rev. 2014 Oct;15(10):822-38. doi: 10.1111/obr.12201. Epub 2014 Jul 11.
- Wilmot EG, Edwardson CL, Achana FA, Davies MJ, Gorely T, Gray LJ, Khunti K, Yates T, Biddle SJ. Sedentary time in adults and the association with diabetes, cardiovascular disease and death: systematic review and meta-analysis. Diabetologia. 2012 Nov;55(11):2895-905. doi: 10.1007/s00125-012-2677-z. Epub 2012 Aug 14. Erratum In: Diabetologia. 2013 Apr;56(4):942-3.
- Kazi A, Duncan M, Clemes S, Haslam C. A survey of sitting time among UK employees. Occup Med (Lond). 2014 Oct;64(7):497-502. doi: 10.1093/occmed/kqu099. Epub 2014 Aug 18.
- Kessler RC, Barber C, Beck A, Berglund P, Cleary PD, McKenas D, Pronk N, Simon G, Stang P, Ustun TB, Wang P. The World Health Organization Health and Work Performance Questionnaire (HPQ). J Occup Environ Med. 2003 Feb;45(2):156-74. doi: 10.1097/01.jom.0000052967.43131.51.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- SHU-AWS-RCT
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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