StandUP UBC: Reducing Workplace Sitting

Not Applicable

Completed

• Conditions: Sedentary Lifestyle
• Interventions: Behavioral: Waitlist control; Behavioral: Standing desk intervention

• Registration Number: NCT03375749
• Lead Sponsor: University of British Columbia

Brief Summary

Research indicates that sedentary behaviours, such as prolonged sitting, have negative health consequences and increases risk for disease. Unfortunately, many office-workers spend a high proportion of their workday sitting, often in prolonged unbroken bouts. Recent interventions have provided active workstations (e.g., sit-stand desks) to reduce employee sitting. However, cost prohibits provision of these desks in work environments. There is a need for low-cost solutions to reduce sitting at work. The purpose of this study is to determine whether provision of a low-cost standing desk reduces workplace sitting, and results in improvements in work engagement and fatigue, compared to usual practice.

Detailed Description

Study objectives: This study aims to provide a cost-effective solution to reducing sitting time during the workday, through provision of (1) low-cost cardboard standing desks ($20), and (2) simple behaviour change strategies (e.g., instruction on how to break up sitting time and information on the health consequences of doing so).

Background: Sedentary behaviour, defined as 'any waking behaviour characterised by an energy expenditure ≤1.5 metabolic equivalents while in a sitting, reclining, or lying posture', is a risk factor for poor health, independent of moderate-to-vigorous physical activity (MVPA). High levels of sedentary behaviour and excessive bouts of prolonged sitting is associated with increased risk for developing type 2 diabetes, cardiovascular disease and some cancers.

Sedentary behaviours are prevalent among Canadian adults, who often spend a large proportion of their waking hours sitting (e.g., work, commuting, watching TV), and office workers have been identified as one of the most sedentary occupational groups. Sedentary behaviour can be reduced by replacing sitting time with standing or light ambulation. In order to do so, it is vital to create an environment that makes sitting less likely and standing/moving easier. There is some evidence that introduction of sit-stand desks can reduce occupational sitting time within office environments ; however, there are cost barriers to the provision of these desks in work environments and few randomized control trials have demonstrated the long-term compliance and effectiveness of these desks on health- (e.g., weight, waist circumference, blood-derived biomarkers, musculoskeletal symptoms, fatigue) and work-related (e.g., work performance/productivity) outcomes. These are important factors that need to be considered and studied in further detail to quantify the benefit of sit-stand workstations.

Therefore, the purpose of this study is to evaluate the long-term effectiveness of a low-cost intervention aimed at reducing workplace sitting time in office workers.

Primary objectives:

• To evaluate the effectiveness of the intervention at reducing daily occupational sitting time over 6 months.

Secondary objectives:

• To explore whether the intervention results in improvements in work engagement and productivity, and occupational fatigue.

Methods/Design: The intervention will be delivered and evaluated over a 6-month period. This study is a two-arm randomized waitlist-controlled trial with one intervention group and one control group. After eligibility assessment, individuals will be randomly allocated to either the intervention or the control arm. The experimental group participants will receive a low-cost cardboard standing desk converter in their regular office environment and behaviour change strategies to break up sitting time, while the control group participants will not encounter any change to their regular work environments or be provided with any behaviour change strategies.

Intervention for experimental group:

Each participant allocated to the experimental group will receive a low-cost, cardboard, fixed-height standing desk converter (https://oristand.co/) that will be placed in their regular office environment, along with their usual sitting desk. The participants will be instructed on how to use the fixed-height standing desk converter (herein referred to as standing desk) as a way to break up sitting time every 30 minutes. In addition, each participant will be provided with information about the health benefits of breaking up sitting time.

Waitlist Control group:

Control group participants will not encounter any changes to their regular office environment. They will be provided with the standing desk and behaviour change strategies 6-months post-intervention.

Study Timeline

• Study First Submitted: 2017-12-12
• Study First Submitted QC: 2017-12-12
• Study First Posted: 2017-12-18
• Study Start: 2018-01-15
• Primary Completion: 2018-09-26
• Study Completion: 2018-09-26
• Status Verified: 2018-12
• Last Update Submitted: 2018-12-01
• Last Update Posted: 2018-12-04

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 48

Inclusion Criteria

• (1) individuals who are desk-based (>75% of seated working hours),
• (2) work at least three days a week using the same desk,
• (3) aged 18-64 years, and
• (4) have the capability of standing.

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Exclusion Criteria

• (1) individuals who are not predominantly desk-based (<75% seated working hours),
• (2) work less than three days a week in the same office, or will not be working for the full duration of the study (i.e., retirement, term-time only, maternity/extended leave),
• (3) self-report having severe musculoskeletal conditions which restrict them from standing,
• (4) already use a standing desk.
• (5) unable to read or understand English or provide full informed consent.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Waitlist Control	Waitlist control	Control group participants will not encounter any changes to their regular office environment. They will be provided with the standing desk and behaviour change strategies 6-months post-intervention.
Standing Desk Intervention	Standing desk intervention	Each participant allocated to the experimental group will receive a low-cost, cardboard, fixed-height standing desk converter (https://oristand.co/) that will be placed in their regular office environment, along with their usual sitting desk. The participants will be instructed on how to use the fixed-height standing desk converter (herein referred to as standing desk) as a way to break up sitting time every 30 minutes. In addition, each participant will be provided with information about the health benefits of breaking up sitting time.

Primary Outcome Measures

Name	Time	Method
Reduction in sitting time	Baseline, 3 months and 6 months	Daily minutes sitting time measured with an activPAL3 micro activity monitor
Reduced number of prolonged sitting bouts (>30 min)	Baseline, 3 months and 6 months	Number of daily bouts of sitting (\>30 mins) measured with an activPAL3 micro activity monitor

Secondary Outcome Measures

Name	Time	Method
Work engagement	Baseline, 3 months and 6 months	Utrecht Work Engagement Scale (UWES). Work engagement will be measured using the Utrecht Work Engagement Scale (UWES), a 7-point likert scale ("never" \[0\]to "always" \[6\]). There are three sub-scales: vigour, dedication, and absorption. The mean scale score of the three UWES subscales is computed by adding the 3 scores on each particular scale and dividing the sum by the number of items of the subscale involved. A similar procedure is followed for the total score. Hence, the UWES yields three subscale scores and/or a total score that range between 0 and 6. Higher values reflect better outcomes.
Occupational fatigue	Baseline, 3 months and 6 months	Need for Recovery (NFR) scale. Occupational fatigue will be measured using the 11-item Need for Recovery (NFR) scale. Indicators of fatigue assessed on the NFR scale include a lack of concentration and reduced motivation for activities at the end of the day. Participants are given dichotomous response options (yes/no) to answer whether or not they experience each indicator. The total number of indicators present for each individual is converted into a scale score which ranges from 0 to 100, where higher scores show a greater need for recovery and thereby greater short-term work-related fatigue.

Trial Locations

Locations (1)

University of British Columbia; 🇨🇦 Vancouver, British Columbia, Canada