Increasing Workplace Physical Activity in Sedentary Office Workers

October 30, 2019 updated by: University of Minnesota

Purpose:

The purpose of this study is to implement and evaluate a randomized controlled trial in sitting office workers to reduce sitting time through the use of motorized and non-motorized sit/stand workstations as well as a walking intervention.

Hypotheses:

  1. Compared to the control group, total physical activity will be higher in the standing and walking intervention groups.
  2. The combined standing and walking group will have higher total physical activity than the other three groups.
  3. Compared to the control group, the fitness and health outcomes will be improved for the standing and walking groups.

Study Overview

Study Type

Interventional

Enrollment (Actual)

260

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

    • Minnesota
      • Minneapolis, Minnesota, United States, 55454
        • University of Minnesota
      • Saint Paul, Minnesota, United States, 55108
        • Fairview Energy Park
      • Saint Paul, Minnesota, United States, 55164
        • MN Department of Human Services

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 and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Sedentary adults who use a single computer workstation for the majority of their workday
  • Work full time (at least 35 hours per week)
  • Must have ability to safely begin a standing and/or walking protocol with no adverse side effects

Exclusion Criteria:

  • Musculoskeletal or joint problems
  • Severe autoimmune conditions
  • Varicose veins that may cause pain
  • Women who are pregnant

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: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Stand
Stand at least half of the workday at work.
Experimental: Move
Increase movement time at work. Move more by making small changes (walking meetings, take stairs, etc).
Experimental: Stand and Move
Increase standing time to half of workday (4h) and increase movement time at work.
No Intervention: General Wellness

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Total physical activity
Time Frame: 6-months
6-months

Secondary Outcome Measures

Outcome Measure
Time Frame
Fasting blood glucose
Time Frame: 6-months
6-months

Other Outcome Measures

Outcome Measure
Time Frame
Total cholesterol
Time Frame: 6-months
6-months
Body composition
Time Frame: 6-months
6-months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Mark A Pereira, PhD, University of Minnesota
  • Principal Investigator: Katie C Carpenter, PhD, University of Minnesota
  • Principal Investigator: Amanda R Bonikowske, MA, University of Minnesota

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

February 1, 2013

Primary Completion (Actual)

March 1, 2014

Study Completion (Actual)

March 1, 2014

Study Registration Dates

First Submitted

April 30, 2013

First Submitted That Met QC Criteria

April 30, 2013

First Posted (Estimate)

May 3, 2013

Study Record Updates

Last Update Posted (Actual)

November 1, 2019

Last Update Submitted That Met QC Criteria

October 30, 2019

Last Verified

October 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • 1212M25961
  • UL1TR000114 (U.S. NIH Grant/Contract)

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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