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Workstation Pilot Study

WorkStation Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01587092
Enrollment
41
Registered
2012-04-27
Start date
2012-08-31
Completion date
2013-02-28
Last updated
2022-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity, Sedentary Lifestyle

Keywords

walking, physical activity, sedentary behavior, workplace

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.

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.

Interventions

BEHAVIORALWorkStation

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.

BEHAVIORALUsual Working Condition

Participants will be asked to continue working at their desk in their usual manner.

Sponsors

Pennington Biomedical Research Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Males or females * BMI ≥ 25 kg/m2 * Willing to give informed consent * Willing to accept randomization to group assignment and willing to follow the protocol for the group to which they have been assigned * Willing to maintain fulltime employment at the company for the next 6 months * Willing to receive frequent contacts and communication from study staff over the next 6 months

Exclusion criteria

* Current participation in other Pennington Biomedical research studies * BMI \< 25 kg/m2 * Type 1 diabetes * Average step count of ≥ 7,500 steps/day * Self-reporting exercising \> 20 minutes on 3 or more days/wk, within the past 6 months * Unable to walk 45 minutes continuously without taking a rest * Unable to walk without the use of an assistive device, such as a cane or walker * Have had a cardiovascular event (stroke or heart attack) in the past 6 months * Have a pacemaker or any other internal electrical medical device * Have been diagnosed with Schizophrenia or bipolar disorder * Have any condition that would limit participation in a physical activity program * Women who are pregnant, have been pregnant in the last 6 months, or are breastfeeding * Actively participating in a weight loss program * 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 * Have another member of household participating in the study * Have any condition, which, in the opinion of the investigator would impede competence or compliance or possibly hinder completion of the study

Design outcomes

Primary

MeasureTime frameDescription
Waist6 monthsWaist circumference will decrease in workers assigned to the WorkStation working condition relative to the usual working condition.

Secondary

MeasureTime frameDescription
Body Fat Percent6 monthsBody fat percent will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
Accelerometry6 monthsParticipants' activity level measured by the accelerometer will increase in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
Gait Speed6 monthsParticipants' gait speed will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
Weight Assessments6 monthsWeight will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
Fatigue6 monthsParticipants' fatigue level will decrease in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
Quality of life Questionnaire6 monthsParticipants' quality of life will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
Stress6 monthsParticipants' stress level will decrease in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026