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

Sedentary Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01863056
• Other study ID #: 1112M07302
• Status: Completed
• Phase: N/A
• Start date: January 2012
• Est. completion date: July 2013

Study information

• Verified date: April 2023
• Source: University of Minnesota
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 29
• Est. completion date: July 2013
• Est. primary completion date: April 2012
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Sedentary

Intervention

Other:
• Sit-Stand Desk
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.

Locations

Country	Name	City	State
United States	Caldrea Inc.	Minneapolis	Minnesota

Sponsors (2)

Lead Sponsor	Collaborator
University of Minnesota	Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Non-Exercise Activity (1 year follow-up)	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.
Primary	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	Ecological Momentary Assesment Fatigue, appetite, energy levels Sitting/standing, Fatigue, appetite, energy levels Self-administered web-based ecological momentary assessments	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
Secondary	24 hr Diet recall	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
Secondary	24 hour Physical Activity Recall	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
Secondary	Productivity Survey	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
Secondary	Stress	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
Secondary	Focus Group Sessions to Qualitatively ascertain experience with Sit-Stand Desks	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
Secondary	Individual Interviews to Qualitatively ascertain experience with Sit-Stand Desks	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
Secondary	Body composition and fitness	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