Skip to main content
Clinical Trials/NCT02376504
NCT02376504CompletedNot Applicable

Modifying the Workplace to Decrease Sedentary Behavior and Improve Health

Northeastern University1 site in 1 country66 target enrollmentStarted: April 2014Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
66
Locations
1
Primary Endpoint
Change in Weight

Study Overview

Brief Summary

The primary objective of this project is to determine the effects of decreasing sedentary behavior at work by at least 3hrs/day using treadmill (walking and standing) and sit-to-stand (standing only) workstations on the health of overweight office workers.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Body Mass Index greater than 25 kg.m-2
  • Does not engage in any structured physical activity lasting at least 30 mins for more than 2 days/week
  • Employed in a full-time sedentary desk job.
  • No major orthopedic limitations or medical conditions that prevents walking or standing at a treadmill work sit-stand workstation.

Exclusion Criteria

  • Not provided

Arms & Interventions

Treadmill workstation

Experimental

Participants will be provided with a treadmill workstation to be more active at the workplace Active Workplace

Intervention: Active workplace (Behavioral)

Sit-to-Stand workstation

Experimental

Participants will be provided with a sit-to-stand workstation to be decrease sitting time at the workplace Active Workplace

Intervention: Active workplace (Behavioral)

Control

No Intervention

Participants will be asked to engage in three 10 min walking bouts each work day

Outcomes

Primary Outcomes

Change in Weight

Time Frame: Baseline, 3, 6, 12 months

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dinesh John

Assistant Professor

Northeastern University

Study Sites (1)

Loading locations...

Similar Trials