- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01787643
Standing Behavior After Installation of Height-Adjustable Desks
January 18, 2022 updated by: USDA Grand Forks Human Nutrition Research Center
Adoption of Standing Behavior After Installation of Height-Adjustable Desks
The purpose of this research study is to determine whether height-adjustable desks change sitting and standing time at work and away from work, engery expenditure, dietary intake, and body composition.
Intermittent peroids of standing made possible by height-adjustable desks may help to impart long-term health benefits.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
14
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
-
-
North Dakota
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Grand Forks, North Dakota, United States, 58203
- USDA Grand Forks Human Nutrition Research Center
-
-
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 to 99 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Being one of the 18 scientists and support staff who have sedentary jobs
- Voluntarily make the choice to replace their current fixed-height sitting desk for a sit-to-stand height-adjustable desk
- Consents to study conditions
Exclusion Criteria:
- Cannot stand for any type of health of orthopedic reasons
- Do not work fulltime
- Pregnant at baseline or become pregnant during the study
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: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Standing desk
Installation of standing desk
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Workplace sitting time to be reduced
Time Frame: 12 months
|
Workplace sitting time will be reduced by 60 minutes across an 8 hour work day and this time will be replaced by standing.
|
12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Total sitting time will be reduced
Time Frame: 12 months
|
Total sitting time will be reduced by 30 minutes across a 16 hour day.
Decreased sitting during the weekday will not be fully compensated for by increased sitting during nonwork hours.
|
12 months
|
Energy expenditure will increase
Time Frame: 12 months
|
Energy expenditure will increase across an 8 hour workday and a 16 hour day.
|
12 months
|
Health behavior change of consuming a lower fat diet
Time Frame: 12 months
|
The non-targeted health behavior of consuming a lower fat diet will co-occur with standing behavior.
Increases in standing behavior will be inversely correlated with changes in total dietary fat intake.
|
12 months
|
Body weight, BMI, and fat mass reduction
Time Frame: 6 months
|
Body weight, BMI, and fast mass will be reduced by 6 months.
|
6 months
|
Changes in musculoskeletal symptoms
Time Frame: 12 months
|
Increases in standing behavior will be correlated with changes in musculoskeletal symptoms.
|
12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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, 2013
Primary Completion (Actual)
August 1, 2014
Study Completion (Actual)
August 1, 2015
Study Registration Dates
First Submitted
February 6, 2013
First Submitted That Met QC Criteria
February 6, 2013
First Posted (Estimate)
February 8, 2013
Study Record Updates
Last Update Posted (Actual)
February 2, 2022
Last Update Submitted That Met QC Criteria
January 18, 2022
Last Verified
January 1, 2022
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- GFHNRC702
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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