A Mixed-methods Evaluation of Sit-stand Workstations in an Office Setting
1 other identifier
interventional
47
1 country
1
Brief Summary
The purpose of this study is to investigate whether a device that allows office workers to sit or stand whilst working can reduce their sitting time at work and improve their health over 8 weeks.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Aug 2013
Shorter than P25 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
August 1, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2013
CompletedFirst Submitted
Initial submission to the registry
July 8, 2015
CompletedFirst Posted
Study publicly available on registry
July 14, 2015
CompletedJuly 14, 2015
July 1, 2015
4 months
July 8, 2015
July 13, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change from baseline in workplace sitting time at 4 and 8 weeks
An ecological momentary assessment (EMA) diary assessed time spent sitting, standing, walking and in other activities during work hours over 5 days (Monday-Friday). At 15-minute intervals participants used a diary to record their main behaviour in response to the question: "What are you doing right now?" The options were sitting, standing, walking or other. If other was selected, participants were instructed to write the activity they were doing. Time spent in each behaviour per day was estimated by multiplying the frequency of recordings by 15. A diary day was considered valid if data entries were provided for ≥75% of time spent at work. Time spent in each behaviour was calculated for each valid day and means were calculated from valid days. To be retained for analyses, participants had to provide ≥2 valid days at each time point.
Baseline (week 0), Mid-intervention (4 weeks), End-intervention (8 weeks)
Secondary Outcomes (15)
Change from baseline in workplace standing time at 4 and 8 weeks
Baseline (week 0), Mid-intervention (4 weeks), End-intervention (8 weeks)
Change from baseline in workplace walking time at 4 and 8 weeks
Baseline (week 0), Mid-intervention (4 weeks), End-intervention (8 weeks)
Change from baseline in flow-mediated dilation (FMD) at 8 weeks
Baseline (week 0), End-intervention (8 weeks)
Change from baseline in carotid artery intima media thickness (cIMT) at 8 weeks
Baseline (week 0), End-intervention (8 weeks)
Change from baseline in plasma glucose at 8 weeks
Baseline (week 0), End-intervention (8 weeks)
- +10 more secondary outcomes
Study Arms (2)
Intervention
EXPERIMENTALProvision of a sit-stand workstation for use at work.
Control
NO INTERVENTIONParticipants were asked to maintain their normal work practices and received no intervention. Participants were offered the opportunity to have a sit-stand workstation installed for 8 weeks after all data collection.
Interventions
After baseline, each participant had a sit-stand workstation installed on their existing workplace desk. A single or dual monitor WorkFit-A with Worksurface+ workstation was installed, dependent on the number of monitors. The monitor(s) and keyboard were housed on the workstation and the workstation could be quickly raised up and down by hand to enable seated or standing work. Participants were not prescribed an amount of time to use the station. Ergotron Ltd provided and installed the workstations and gave participants basic face-to-face training and ergonomic information on correct use. Participants received a web link to manufacturer ergonomic guidelines via an email from the research team. After end-intervention data collection, manufacturer staff uninstalled the workstations.
Eligibility Criteria
You may qualify if:
- full-time member of staff
- access to a work telephone and desktop computer with internet
You may not qualify if:
- have a cardiovascular or metabolic disease
- taking any medication
- pregnant
- planned absence \> 1 week during the trial
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Liverpool John Moores University
Liverpool, Merseyside, L3 2AT, United Kingdom
Related Publications (3)
Batterham AM, Hopkins WG. Making meaningful inferences about magnitudes. Int J Sports Physiol Perform. 2006 Mar;1(1):50-7.
PMID: 19114737RESULTHopkins WG, Marshall SW, Batterham AM, Hanin J. Progressive statistics for studies in sports medicine and exercise science. Med Sci Sports Exerc. 2009 Jan;41(1):3-13. doi: 10.1249/MSS.0b013e31818cb278.
PMID: 19092709RESULTE F Graves L, C Murphy R, Shepherd SO, Cabot J, Hopkins ND. Evaluation of sit-stand workstations in an office setting: a randomised controlled trial. BMC Public Health. 2015 Nov 19;15:1145. doi: 10.1186/s12889-015-2469-8.
PMID: 26584856DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Lee EF Graves, PhD
Liverpool John Moores University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer/Senior Lecturer
Study Record Dates
First Submitted
July 8, 2015
First Posted
July 14, 2015
Study Start
August 1, 2013
Primary Completion
December 1, 2013
Study Completion
December 1, 2013
Last Updated
July 14, 2015
Record last verified: 2015-07