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Completed

NCT Number: NCT01587092

Workstation Pilot Study

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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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Pennington Biomedical Research Center

Baton Rouge, Louisiana, 70808, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

WorkStation

Behavioral

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.

Usual Working Condition

Behavioral

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

Primary outcomes

  1. Waist

    Time frame: 6 months

    Waist circumference will decrease in workers assigned to the WorkStation working condition relative to the usual working condition.

Secondary outcomes

  1. Weight Assessments

    Time frame: 6 months

    Weight will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.

  2. Body Fat Percent

    Time frame: 6 months

    Body fat percent will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.

  3. Accelerometry

    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.

  4. Gait Speed

    Time frame: 6 months

    Participants' gait speed will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.

  5. Stress

    Time frame: 6 months

    Participants' stress level will decrease in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.

  6. Fatigue

    Time frame: 6 months

    Participants' fatigue level will decrease in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.

  7. Quality of life Questionnaire

    Time frame: 6 months

    Participants' quality of life will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.

Sponsors and collaborators

Lead sponsor

Pennington Biomedical Research Center

Other

Registry information

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Apr 27, 2012
Registry last updated
Sep 15, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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