Pennington Biomedical Research Center
Baton Rouge, Louisiana, 70808, United States
NCT Number: NCT01587092
This is a pilot study to assess the feasibility of using treadmill desks (Workstations) within a Louisiana office workplace and to determine the effects of walking while working in overweight or obese, sedentary individuals.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Baton Rouge, Louisiana, 70808, United States
Eligible participants will be randomized by chance to the WorkStation Intervention Group or to a Usual Working Condition Group.
The WorkStation Intervention Group will be asked to walk for up to 1.5 hours per day during the work week of Monday through Friday on the treadmill. Participants will complete two sessions per day for up to 45 minutes per session, tracking time and speed.
Usual Working Condition Group will be asked to continue working in usual environment and accustomed manner.
Regardless of which group the participants are assigned to, the participants will be asked to complete baseline and follow up assessment visits. Months 3 and 6 for approximately 1 hour for Body measurements (height, weight and waist circumference), body fat percent, gait speed, questionnaires, and accelerometry.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will be asked to attend 2 scheduled sessions per day of treadmill walking, which will replace their sitting desk time. Participants will complete 2 sessions per day for 6 months.
Participants will be asked to continue working at their desk in their usual manner.
Time frame: 6 months
Waist circumference will decrease in workers assigned to the WorkStation working condition relative to the usual working condition.
Time frame: 6 months
Weight will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
Time frame: 6 months
Body fat percent will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
Time frame: 6 months
Participants' activity level measured by the accelerometer will increase in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
Time frame: 6 months
Participants' gait speed will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
Time frame: 6 months
Participants' stress level will decrease in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
Time frame: 6 months
Participants' fatigue level will decrease in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
Time frame: 6 months
Participants' quality of life will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
Pennington Biomedical Research Center
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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