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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02172599
Other study ID # TSWH
Secondary ID R33134
Status Completed
Phase N/A
First received June 22, 2014
Last updated January 17, 2018
Start date May 2014
Est. completion date February 2016

Study information

Verified date January 2018
Source Brunel University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date February 2016
Est. primary completion date February 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Sit-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.

Locations

Country Name City State
United Kingdom Macmillan Cancer Support UK Office London
United Kingdom Public Health England, SKipton House London

Sponsors (4)

Lead Sponsor Collaborator
Brunel University Ergotron, Macmillan Canceer Support, Public Health England

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Physical Activity ActivPAL:
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).
Measured 5 times over 13 months, for seven days each time. Time points = baseline, 1-2weeks, 3 months, 6 months and 12 months
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