Effects of Installing Height-adjustable Workstations on Office Workers Workplace Sitting Time and Productivity

Sponsor
Sheffield Hallam University (Other)
Overall Status
Completed
CT.gov ID
NCT02932787
Collaborator
(none)
31
2
23

Study Details

Study Description

Brief Summary

The purpose of this study was to look at the effects that height-adjustable workstations on occupational sitting time and workplace productivity in office workers. Participants workplace activity (sitting, standing and walking) and productivity was measured before the installation of the height-adjustable workstations. Workplace activity and productivity were then measured four weeks after the installation of height-adjustable workstations. The results were compared to a control group who received no intervention whilst the intervention had the height-adjustable workstations.

Condition or Disease Intervention/Treatment Phase
  • Device: Height-adjustable workstation
N/A

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 Design

Study Type:
Interventional
Actual Enrollment :
31 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Effects of Installing Height-adjustable Workstations on Occupational Sitting Time and Workplace Productivity in Desk-based Workers
Study Start Date :
Dec 1, 2013
Actual Primary Completion Date :
Nov 1, 2015
Actual Study Completion Date :
Nov 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Height-adjustable workstation

Participants received a height-adjustable workstation for four weeks

Device: Height-adjustable workstation

No Intervention: Control

Outcome Measures

Primary Outcome Measures

  1. Change in Workplace Sedentary Time [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.

Secondary Outcome Measures

  1. Change in Workplace Absenteeism Using the World Health Organisation Health and Work Performance Questionnaire [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.

  2. Change in Workplace Presenteeism Using the World Health Organisation Health and Work Performance Questionnaire [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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. age 18 to 65 years,

  2. working ≥0.6 full time equivalents,

  3. access to a work telephone and desktop computer with internet,

  4. not pregnant,

  5. no planned absence >1 week during the trial,

  6. not chair-bound or uniquely impaired such that reducing occupational sitting time was not feasible,

  7. no pre-existing musculoskeletal disorder.

Exclusion Criteria:

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Sheffield Hallam University

Investigators

  • Principal Investigator: Simon H Till, Sheffield Hallam University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Sheffield Hallam University
ClinicalTrials.gov Identifier:
NCT02932787
Other Study ID Numbers:
  • SHU-AWS-RCT
First Posted:
Oct 13, 2016
Last Update Posted:
Apr 28, 2020
Last Verified:
Apr 1, 2020

Study Results

Participant Flow

Recruitment Details Office-based workplace (UK)
Pre-assignment Detail
Arm/Group Title Height-adjustable Workstation Control
Arm/Group Description Participants received a height-adjustable workstation for four weeks Height-adjustable workstation
Period Title: Overall Study
STARTED 22 9
COMPLETED 22 9
NOT COMPLETED 0 0

Baseline Characteristics

Arm/Group Title Height-adjustable Workstation Control Total
Arm/Group Description Participants received a height-adjustable workstation for four weeks Height-adjustable workstation Total of all reporting groups
Overall Participants 22 9 31
Age (Count of Participants)
<=18 years
0
0%
0
0%
0
0%
Between 18 and 65 years
22
100%
9
100%
31
100%
>=65 years
0
0%
0
0%
0
0%
Age (years) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [years]
46
(10.3)
37
(7.26)
43.38
(9.42)
Sex: Female, Male (Count of Participants)
Female
12
54.5%
7
77.8%
19
61.3%
Male
10
45.5%
2
22.2%
12
38.7%
Region of Enrollment (Count of Participants)
United Kingdom
22
100%
9
100%
31
100%

Outcome Measures

1. Primary Outcome
Title Change in Workplace Sedentary Time
Description The amount of time a participant spends sitting whilst in the workplace (minutes). This was measured using a thigh-worn ActivPAL accelerometer.
Time Frame Baseline (0 weeks), 4 weeks after installation of height-adjustable workstations

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Height-adjustable Workstation Control
Arm/Group Description Participants that received a height-adjustable workstation Participants that did not receive a height-adjustable workstation
Measure Participants 11 6
Baseline
369
(43.75)
355
(73.69)
4-Weeks after installation
229
(46.35)
338
(70.4)
2. Secondary Outcome
Title Change in Workplace Absenteeism Using the World Health Organisation Health and Work Performance Questionnaire
Description 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.
Time Frame Baseline (0 weeks), 4 weeks after installation of height-adjustable workstations

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Height-adjustable Workstation Control
Arm/Group Description Participants received a height-adjustable workstation for four weeks Height-adjustable workstation Participants that did not receive a height-adjustable workstation
Measure Participants 21 7
Baseline Absenteeism
-4
-8
4-Week Absenteeism
0
0
3. Secondary Outcome
Title Change in Workplace Presenteeism Using the World Health Organisation Health and Work Performance Questionnaire
Description 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.
Time Frame Baseline (0 weeks), 4 weeks after installation of height-adjustable workstations

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Height-adjustable Workstation Control
Arm/Group Description Participants received a height-adjustable workstation Participants that did not received a height-adjustable workstation
Measure Participants 21 7
Baseline Presenteeism
80
80
4-Week Presenteeism
80
90

Adverse Events

Time Frame
Adverse Event Reporting Description
Arm/Group Title Height-adjustable Workstation Control
Arm/Group Description Participants received a height-adjustable workstation for four weeks Participants that did not receive a height-adjustable workstation
All Cause Mortality
Height-adjustable Workstation Control
Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 0/22 (0%) 0/9 (0%)
Serious Adverse Events
Height-adjustable Workstation Control
Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 0/22 (0%) 0/9 (0%)
Other (Not Including Serious) Adverse Events
Height-adjustable Workstation Control
Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 0/22 (0%) 0/9 (0%)

Limitations/Caveats

[Not Specified]

More Information

Certain Agreements

All Principal Investigators ARE employed by the organization sponsoring the study.

There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

Results Point of Contact

Name/Title Martin Lamb
Organization Sheffield Hallam University
Phone 01142552782
Email m.lamb@shu.ac.uk
Responsible Party:
Sheffield Hallam University
ClinicalTrials.gov Identifier:
NCT02932787
Other Study ID Numbers:
  • SHU-AWS-RCT
First Posted:
Oct 13, 2016
Last Update Posted:
Apr 28, 2020
Last Verified:
Apr 1, 2020