- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02566317
Stand & Move at Work
October 9, 2019 updated by: Arizona State University
Stand & Move at Work: A Group Randomized Trial
A trial testing the efficacy of sit-stand workstations on decreasing sitting time and increasing light-intensity physical activity in samples of office worksites.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
With traditional approaches to increasing MVPA (moderate to vigorous physical activity) in the workplace being unsustainable due to the requirement of deliberate and dedicated time away from work, this group-randomized trial will test the efficacy of sit-stand workstations on decreasing sitting time and increasing light-intensity physical activity (LPA) in a highly generalizable sample of office worksites using a multi-level intervention with high potential for dissemination.
Study Type
Interventional
Enrollment (Actual)
630
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
-
-
Arizona
-
Tempe, Arizona, United States, 85281
- Arizona State University
-
-
Minnesota
-
Minneapolis, Minnesota, United States, 55455
- University of Minnesota
-
-
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
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
Worksite-level inclusion criteria:
- Size: Small to moderate size worksite (20-60 employees)
- Schedule: >80% of employees full time
- Occupation: Seated office work, primarily computer- and- telephone-based work, little movement or walking
- Wellness environment: Not currently undergoing a wellness program aimed at increasing activity at work
- Workstations: Willing to have sit-stand workstations installed at a worksite
- Willing to be randomized: Willing to be randomized to either intervention conditions
Member-level inclusion criteria:
- Age: 18 years and older
- Health status: Generally good health and able to safely increase LPA and reduce sitting time
- Employment status: Any sedentary job, sitting most of the say, little standing or walking
- Occupation: Traditional sitting desk, willing to have a sit-stand workstation installed at desk
- Workstation: traditional sitting desk;willing to have a sit-stand workstation installed at desk
Exclusion Criteria:
- contraindication to prolonged standing at work
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: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Move
A multi-level individual, social, environmental, and organizational intervention targeting increases in light-intensity physical activity in the workplace.
|
A multi-level individual, social, environmental, and organizational intervention targeting increases in light-intensity physical activity in the workplace
|
Experimental: Stand & Move
Move intervention (A multi-level individual, social, environmental, and organizational intervention targeting increases in light-intensity physical activity in the workplace) plus the installation of a sit-stand workstation.
|
A multi-level individual, social, environmental, and organizational intervention targeting increases in light-intensity physical activity in the workplace
Installation of a sit-stand desk at work
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Mean Change in Light-intensity Physical Activity at Work From Baseline to 12 Months
Time Frame: 1 year
|
Measured via 7d of activPAL accelerometry (value at 12 months minus value at baseline)
|
1 year
|
Mean Change in Sitting Time at Work From Baseline to 12 Months
Time Frame: 1 year
|
Measured via 7d of activPAL accelerometry (value at 12 months minus value at baseline)
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Clustered Metabolic Risk Score From Baseline to 12 Months
Time Frame: 1 year
|
Clustered metabolic risk score (fasting glucose, insulin, triglycerides, HDL-cholesterol, blood pressure); value at 12 months minus value at baseline; higher scores indicate better outcome.
The Z-score for each component (fasting glucose, insulin, triglycerides, HDL-cholesterol, blood pressure) based on the baseline mean and standard deviation of the entire group was computed and summed for each participant (HDL z-score was subtracted rather than added).
The sum of these z-scores represents the metabolic risk score.
|
1 year
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Sleep Substudy
Time Frame: 1 year
|
24h wrist accelerometry in individuals with minor-moderate sleep complaints
|
1 year
|
Ambulatory Blood Pressure
Time Frame: 3 months
|
Dynamic changes in ambulatory blood pressure in prehypertensives
|
3 months
|
Ecological Momentary Assessment of Mood
Time Frame: 1 year
|
Periodic monitoring of mood, energy, fatigue in smartphone users
|
1 year
|
Dynamic Glucose Control
Time Frame: 3 months
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Continuous glucose monitoring in prediabetics
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Matthew P Buman, PhD, Arizona State University
- Principal Investigator: Mark A Pereira, PhD, University of Minnesota
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.
General Publications
- Leonard KS, Mullane SL, Golden CA, Rydell SA, Mitchell NR, Koskan A, Estabrooks PA, Pereira MA, Buman MP. Qualitative comparative analysis of the implementation fidelity of a workplace sedentary reduction intervention. BMC Public Health. 2022 May 31;22(1):1086. doi: 10.1186/s12889-022-13476-3.
- Pereira MA, Mullane SL, Toledo MJL, Larouche ML, Rydell SA, Vuong B, Feltes LH, Mitchell NR, de Brito JN, Hasanaj K, Carlson NG, Gaesser GA, Crespo NC, Oakes JM, Buman MP. Efficacy of the 'Stand and Move at Work' multicomponent workplace intervention to reduce sedentary time and improve cardiometabolic risk: a group randomized clinical trial. Int J Behav Nutr Phys Act. 2020 Oct 27;17(1):133. doi: 10.1186/s12966-020-01033-3.
- Mullane SL, Toledo MJL, Rydell SA, Feltes LH, Vuong B, Crespo NC, Pereira MA, Buman MP. Social ecological correlates of workplace sedentary behavior. Int J Behav Nutr Phys Act. 2017 Aug 31;14(1):117. doi: 10.1186/s12966-017-0576-x.
- Buman MP, Mullane SL, Toledo MJ, Rydell SA, Gaesser GA, Crespo NC, Hannan P, Feltes L, Vuong B, Pereira MA. An intervention to reduce sitting and increase light-intensity physical activity at work: Design and rationale of the 'Stand & Move at Work' group randomized trial. Contemp Clin Trials. 2017 Feb;53:11-19. doi: 10.1016/j.cct.2016.12.008. Epub 2016 Dec 7.
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 (Actual)
January 15, 2016
Primary Completion (Actual)
December 15, 2017
Study Completion (Actual)
December 15, 2018
Study Registration Dates
First Submitted
September 22, 2015
First Submitted That Met QC Criteria
September 30, 2015
First Posted (Estimate)
October 2, 2015
Study Record Updates
Last Update Posted (Actual)
October 11, 2019
Last Update Submitted That Met QC Criteria
October 9, 2019
Last Verified
October 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01CA198971 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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