The Effect of Sit-Stand Workstations on Physical Activity in Sedentary Office Workers

April 6, 2023 updated by: University of Minnesota

The Effect of Sit-Stand Workstations on Physical Activity in Sedentary Office Workers: A Randomized Crossover Trial

The purpose of this study was to determine whether the installation of sit-stand work stations could lead to decreased sedentary time and increased physical activity during the workday among sedentary office workers.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

29

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Minnesota
      • Minneapolis, Minnesota, United States, 55405
        • Caldrea Inc.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Mostly sedentary (sitting ≥ 4 hour) during the workday.
  • Age ≥ 18
  • Anticipated using a single computer workstation for 20 hours or more per week

Exclusion Criteria:

  • Unable to stand for at least two hours per workday (two hours over the whole workday, not consecutively)
  • Reported severe musculoskeletal symptoms, specifically lower extremity or lower back pain.
  • Diagnosed with or under treatment for diabetes, heart disease, cancer, orthostatic hypertension, varicose vein, autoimmune disease, or other chronic diseases.
  • Pregnant women

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Sit-Stand Desk
Cross-over trial: so one group got the intervention in period 1 and didn't get the intervention in period 2 (serving as control for self in period 2) and the other group got the intervention in period 2 and didn't get the intervention in period 1 (serving as control for self in period 1).
Subjects were asked to participate in the study for a total period of three months. Based on randomization, either the first or third month involved the active intervention to use an adjustable sit-stand desk. The other two months required the subjects to follow their usual work routine without the adjustable sit-stand desk. The control period month involved all the same measurements as the active intervention month, whereas the washout period, which was the 2nd (middle) month, did not involve any measurement and there was no contact with the subjects during the washout month.
No Intervention: Control
Used normal work desk which only allows working sitting down

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
non-exercise activity
Time Frame: Measured constantly during the entire control period and measured constantly during the entire intervention period and the two periods were compared to determine change in non-exercise activity

Non-exercise activity was meausred by triple axis accelerometers during all waking hours in the control period (1 month) and in the intervention period (1 month). The two periods were then compared for each subject.

Sitting time was also measured subjectively using a validated questionnaire: occupational sitting and physical activity questinnarie (OSPAQ)

Hypothesis: Amount of time spent standing, walking, and other components of non-exercise activity will be higher during the standing intervention period relative to the control period (usual sitting).

Measured constantly during the entire control period and measured constantly during the entire intervention period and the two periods were compared to determine change in non-exercise activity

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Ecological Momentary Assesment Fatigue, appetite, energy levels Sitting/standing, Fatigue, appetite, energy levels Self-administered web-based ecological momentary assessments
Time Frame: Twice per day during workdays (5 days a week) for 4 weeks of control period and 4 weeks of intervention period and the two periods were compared

Sitting/standing,Fatigue, appetite, energy levels etc. were measured via quick ecological momentary assessment surveys. These are all part of one short questionnaire that participants filled out twice a day during the study.

Hypothesis: Self-reported energy levels will be higher and fatigue will be lower for the standing intervention period compared to control.

Twice per day during workdays (5 days a week) for 4 weeks of control period and 4 weeks of intervention period and the two periods were compared
24 hr Diet recall
Time Frame: Once a week for 4 weeks of control period and 4 weeks of intervention period and the two periods were compared
Self-administered web-based 24 hour dietary recall Hypothesis: Energy intake will not be higher and eating behaviors will not be different (e.g., meal/snack size, frequency, and composition) between the standing intervention periods and control.
Once a week for 4 weeks of control period and 4 weeks of intervention period and the two periods were compared
24 hour Physical Activity Recall
Time Frame: Once a week for 4 weeks of control period and 4 weeks of intervention period and the two periods were compared
On a random day a week, subjects filled out what they did for every 15 minute increment for the last 24 hours.
Once a week for 4 weeks of control period and 4 weeks of intervention period and the two periods were compared
Productivity Survey
Time Frame: Once a week for 4 weeks of control period and 4 weeks of intervention period and the two periods were compared
The Work Productivity and Activity Impairment Questionnaire was used to assess productivity in the previous week.
Once a week for 4 weeks of control period and 4 weeks of intervention period and the two periods were compared
Stress
Time Frame: Once every two weeks for 4 weeks of control period and 4 weeks of intervention period and the two periods were compared
The Perceived Stress Scale was used to measure stress level every two weeks.
Once every two weeks for 4 weeks of control period and 4 weeks of intervention period and the two periods were compared
Focus Group Sessions to Qualitatively ascertain experience with Sit-Stand Desks
Time Frame: End of Study

Focus group sessions were conducted to ascertain the experience of switching to sit-stand workstations for people who participated in the study and for people who did not participate in the study (what it was like to have co-workers use sit-stand desks).

This is a qualitative measure without hard outcomes. Questions were asked about overall experience with sit-stand desks (SSDs), benefits and drawbacks of use, whether they see themselves using the SSDs regularly in the long run, things they liked, things they did not like, health effects of standing, and impact of standing on interaction with coworkers.

End of Study
Individual Interviews to Qualitatively ascertain experience with Sit-Stand Desks
Time Frame: End of control period and end of intervention period

Individual interviews were conducted to ascertain the experience of switching to a sit-stand workstation.

This is a qualitative measure without hard outcomes. Questions were asked about overall experience with sit-stand desks (SSDs), benefits and drawbacks of use, whether they see themselves using the SSDs regularly in the long run, things they liked, things they did not like, health effects of standing, and impact of standing on interaction with coworkers.

End of control period and end of intervention period
Body composition and fitness
Time Frame: Beginning of control period, end of control period (4 weeks later), beginning of intervention period, and end of intervention period

Body composition (DXA scan), height, weight, waist-to-hip-ratio, and cardiovascular fitness (treadmill walk and step test) were performed to measure physical changes.

Women without a history of histerectomy underwent urine pregnancy test before going for the DXA scan. baseline fitness and health status of all participants were assessed by a study physician to ensure that subjects were able to participate in the fitness tests.

Beginning of control period, end of control period (4 weeks later), beginning of intervention period, and end of intervention period

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Non-Exercise Activity (1 year follow-up)
Time Frame: 1 Year follow-up after the end of the main study. it will be for 1 week of constant measurement of non-exercise activity.

Non-exercise activity will be measured again by by triple axis accelerometers like in the main study.

Sitting time will also be measured subjectively using a validated questionnaire: occupational sitting and physical activity questinnarie (OSPAQ).

Diet, feelings survey (ecological momentary assesment), physical activity, stress, productivity, and other related things may also be measured during that week. Individual interviews and focus group sessions will also be conducted at this time point.

1 Year follow-up after the end of the main study. it will be for 1 week of constant measurement of non-exercise activity.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Mark Pereira, Ph.D., School of Public Health, University of Minnesota, Minneapolis

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2012

Primary Completion (Actual)

April 1, 2012

Study Completion (Actual)

July 1, 2013

Study Registration Dates

First Submitted

April 24, 2013

First Submitted That Met QC Criteria

May 22, 2013

First Posted (Estimate)

May 27, 2013

Study Record Updates

Last Update Posted (Actual)

April 7, 2023

Last Update Submitted That Met QC Criteria

April 6, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 1112M07302

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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