Skip to content

Take A Stand for Workplace Health: A Sit-stand Workstation Project Evaluation

The Influence of Sit-stand Workstations Upon Total Physical Activity: a 12 Month Randomised Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02172599
Enrollment
30
Registered
2014-06-24
Start date
2014-05-31
Completion date
2016-02-29
Last updated
2018-01-18

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

Conditions

Physical Activity

Keywords

sit-stand workstation, workplace, multi-component intervention, randomised control trial design, physical activity, sitting, sedentary behaviour, process evaluation, health

Brief summary

The purpose of this study is to examine the contribution of sit-stand workstations to total daily physical activity in a multi-component office-based 12 month intervention.

Detailed description

This study adopts a randomised control trial design and is mixed methods (qualitative and quantitative). The outcome data from the trial is quantitative. Alongside this a qualitative process evaluation will be conducted to inform the intervention, explain trial results and understand the intervention implementation and context (Cathain et al. 2014). Two worksites will participate in this study, in line with COCHRANE recommendations for randomised control trials.

Interventions

BEHAVIORALSit-stand workstation provision

The research compares the effects of a sit-stand workstation only and a multi-component sit-stand workstation intervention including individual and organisation-level approaches, with usual office-based working practice (no sit-stand workstation) over 12 months.

Sponsors

Macmillan Canceer Support
CollaboratorOTHER
Ergotron
CollaboratorUNKNOWN
Public Health England
CollaboratorOTHER_GOV
Brunel University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Must be a full-time employee on a fixed term contract for at least 18 months at one of the two worksites involved in the study (Macmillan Cancer Support, Public Health England) * Must engage in primarily desk-based work * Must have their own desk (i.e. does not hot desk) Must be primarily office based (i.e. not working from home) * Must have no plans to leave the organisation for an extended period (e.g. holiday \> 4 weeks or secondment) or finitely before the anticipated study end date (January 2016)

Exclusion criteria

* Have engaged in standing-based desk work in the month prior to the start of the study * Have been advised against standing by a health professional; or be unable to stand * Work for the Macmillan Support Line

Design outcomes

Primary

MeasureTime frameDescription
Physical ActivityMeasured 5 times over 13 months, for seven days each time. Time points = baseline, 1-2weeks, 3 months, 6 months and 12 monthsActivPAL: Sitting and standing will be measured objectively using the ActivPAL device. The ActivPAL provides reliable measures of total sitting time and standing time, and number of sit-to-stand transitions per hour (Lyden et al. 2012). ActiGraph (GT3X+): Physical activity intensity and duration will be measured objectively using the ActiGraph activity monitor.The GT3X reliably classifies physical activity intensity in free-living environments (Ozemek et al. 2014). Activity diaries: These dairies will be used to assess the type and context of physical activity behaviour. A text reminder will be sent to all participants once daily for the duration of the data collection period. Text message models have shown some success in increasing compliance to research (Armstrong et al. 2009).

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026