Workstation Pilot Study
Study Details
Study Description
Brief Summary
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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
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.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Placebo Comparator: Usual Working Condition Group Participants assigned to the usual working condition control group will continue to work in their usual environment and accustomed manner. The control group participants will have access to the Workstations at the completion of study. |
Behavioral: Usual Working Condition
Participants will be asked to continue working at their desk in their usual manner.
|
| Active Comparator: WorkStation Intervention Group Participants will be asked to walk for up to 1.5 hours per day on the treadmill. This will be split into two 45 minute sessions per day. Behavioral support will focus on adherence to frequency (attending scheduled sessions). Participants self-select speed of walking and time (they have up to 45 minutes allotted, but may choose less as they like). |
Behavioral: WorkStation
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.
|
Outcome Measures
Primary Outcome Measures
- Waist [6 months]
Waist circumference will decrease in workers assigned to the WorkStation working condition relative to the usual working condition.
Secondary Outcome Measures
- Feasibility [6 months]
Feasibility will be evaluated by a number of metrics: The number of workers attending orientations (thereby showing interest) Adherence to scheduled WorkStation sessions Impact on productivity metrics Arm-specific exit focus group their experience/perceptions and relative interest in continuing to use the WorkStation
- Weight Assessments [6 months]
Weight will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
- Body Fat Percent [6 months]
Body fat percent will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
- Accelerometry [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.
- Gait Speed [6 months]
Participants' gait speed will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
- Fatigue [6 months]
Participants' fatigue level will decrease in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
- Stress [6 months]
Participants' stress level will decrease in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
- Quality of life Questionnaire [6 months]
Participants' quality of life will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Males or females
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BMI ≥ 25 kg/m2
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Willing to give informed consent
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Willing to accept randomization to group assignment and willing to follow the protocol for the group to which they have been assigned
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Willing to maintain fulltime employment at the company for the next 6 months
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Willing to receive frequent contacts and communication from study staff over the next 6 months
Exclusion Criteria:
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Current participation in other Pennington Biomedical research studies
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BMI < 25 kg/m2
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Type 1 diabetes
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Average step count of ≥ 7,500 steps/day
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Self-reporting exercising > 20 minutes on 3 or more days/wk, within the past 6 months
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Unable to walk 45 minutes continuously without taking a rest
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Unable to walk without the use of an assistive device, such as a cane or walker
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Have had a cardiovascular event (stroke or heart attack) in the past 6 months
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Have a pacemaker or any other internal electrical medical device
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Have been diagnosed with Schizophrenia or bipolar disorder
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Have any condition that would limit participation in a physical activity program
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Women who are pregnant, have been pregnant in the last 6 months, or are breastfeeding
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Actively participating in a weight loss program
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Plan to move out of the study area within the next 6 months or plan to be away from work for more than 4 weeks in the next 6 months
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Have another member of household participating in the study
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Have any condition, which, in the opinion of the investigator would impede competence or compliance or possibly hinder completion of the study
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Pennington Biomedical Research Center | Baton Rouge | Louisiana | United States | 70808 |
Sponsors and Collaborators
- Pennington Biomedical Research Center
- Company wishing not to be named
Investigators
- Principal Investigator: Catrine Tudor-Locke, PhD, Principal Investigator
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- PBRC12015