- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01863056
The Effect of Sit-Stand Workstations on Physical Activity in Sedentary Office Workers
The Effect of Sit-Stand Workstations on Physical Activity in Sedentary Office Workers: A Randomized Crossover Trial
Study Overview
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Minnesota
-
Minneapolis, Minnesota, United States, 55405
- Caldrea Inc.
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
Sponsor
Collaborators
Investigators
- Principal Investigator: Mark Pereira, Ph.D., School of Public Health, University of Minnesota, Minneapolis
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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.
Clinical Trials on Sedentary
-
University of North Carolina, Chapel HillNational Heart, Lung, and Blood Institute (NHLBI)RecruitingSedentary Behavior | Sedentary TimeUnited States
-
Loughborough UniversityBritish Heart FoundationCompletedSedentary Lifestyle | Sedentary Behavior | Diet Habit
-
Eskisehir Technical UniversityThe Scientific and Technological Research Council of TurkeyNot yet recruitingSedentary Lifestyle | Sedentary Behavior | Physical Activity Level
-
Yasin AkCompletedSedentary Time | Sedentary BehaviourTurkey
-
Research on Healthcare Performance Lab U1290RecruitingSedentary Behavior | Sedentary Time | Health Behavior | Health-Related Behavior | Physical InactivityFrance
-
University Hospital, Clermont-FerrandCompletedPregnancy Related | Sedentary Behavior | Sedentary Time | Perinatal Problems | Morbidity;PerinatalFrance
-
Universidade Federal de Sao CarlosCompleted
-
University of ValenciaCompleted
-
University of Massachusetts, WorcesterUniversity of Massachusetts, LowellCompletedSedentaryUnited States
-
Universidad Europea de MadridCompleted
Clinical Trials on Sit-Stand Desk
-
University of Prince Edward IslandCompletedPhysical Activity | Glucose Tolerance | Insulin Sensitivity | Sedentary BehaviourCanada
-
Loughborough UniversityBradford Teaching Hospitals NHS Foundation TrustCompletedObesity | Physical Activity | Child Behavior | Sedentary Behavior | Health Behavior
-
University Hospital, Clermont-FerrandNot yet recruitingOccupational Stress | Sedentary BehaviorFrance
-
Stanford UniversityCompleted
-
Montclair State UniversityEnrolling by invitationOverweight and ObesityUnited States
-
Hamilton Health Sciences CorporationOntario Ministry of Health and Long Term CareUnknownCerebrovascular AccidentCanada
-
Riphah International UniversityRecruitingCerebral PalsyPakistan
-
University of ZurichCompletedHealthy IndividualsSwitzerland
-
University Hospital, RouenUnknown