- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01846013
Increasing Workplace Physical Activity in Sedentary Office Workers
October 30, 2019 updated by: University of Minnesota
Purpose:
The purpose of this study is to implement and evaluate a randomized controlled trial in sitting office workers to reduce sitting time through the use of motorized and non-motorized sit/stand workstations as well as a walking intervention.
Hypotheses:
- Compared to the control group, total physical activity will be higher in the standing and walking intervention groups.
- The combined standing and walking group will have higher total physical activity than the other three groups.
- Compared to the control group, the fitness and health outcomes will be improved for the standing and walking groups.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
260
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, 55454
- University of Minnesota
-
Saint Paul, Minnesota, United States, 55108
- Fairview Energy Park
-
Saint Paul, Minnesota, United States, 55164
- MN Department of Human Services
-
-
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:
- Sedentary adults who use a single computer workstation for the majority of their workday
- Work full time (at least 35 hours per week)
- Must have ability to safely begin a standing and/or walking protocol with no adverse side effects
Exclusion Criteria:
- Musculoskeletal or joint problems
- Severe autoimmune conditions
- Varicose veins that may cause pain
- Women who are pregnant
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: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Stand
|
Stand at least half of the workday at work.
|
Experimental: Move
|
Increase movement time at work.
Move more by making small changes (walking meetings, take stairs, etc).
|
Experimental: Stand and Move
|
Increase standing time to half of workday (4h) and increase movement time at work.
|
No Intervention: General Wellness
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Total physical activity
Time Frame: 6-months
|
6-months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Fasting blood glucose
Time Frame: 6-months
|
6-months
|
Other Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Total cholesterol
Time Frame: 6-months
|
6-months
|
Body composition
Time Frame: 6-months
|
6-months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Mark A Pereira, PhD, University of Minnesota
- Principal Investigator: Katie C Carpenter, PhD, University of Minnesota
- Principal Investigator: Amanda R Bonikowske, MA, University of Minnesota
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
February 1, 2013
Primary Completion (Actual)
March 1, 2014
Study Completion (Actual)
March 1, 2014
Study Registration Dates
First Submitted
April 30, 2013
First Submitted That Met QC Criteria
April 30, 2013
First Posted (Estimate)
May 3, 2013
Study Record Updates
Last Update Posted (Actual)
November 1, 2019
Last Update Submitted That Met QC Criteria
October 30, 2019
Last Verified
October 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- 1212M25961
- UL1TR000114 (U.S. NIH Grant/Contract)
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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