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Increasing Workplace Physical Activity in Sedentary Office Workers

Increasing Workplace Physical Activity in Sedentary Office Workers

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01846013
Enrollment
260
Registered
2013-05-03
Start date
2013-02-28
Completion date
2014-03-31
Last updated
2019-11-01

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

Conditions

Sit-Stand Workstations

Keywords

Sit-Stand Workstations, Increase Workplace Physical Activity

Brief summary

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.

Interventions

BEHAVIORALStand

Stand at least half of the workday at work.

BEHAVIORALMove

Increase movement time at work. Move more by making small changes (walking meetings, take stairs, etc).

BEHAVIORALStand and Move

Increase standing time to half of workday (4h) and increase movement time at work.

Sponsors

Mayo Clinic
CollaboratorOTHER
University of Minnesota
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

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

Design outcomes

Primary

MeasureTime frame
Total physical activity6-months

Secondary

MeasureTime frame
Fasting blood glucose6-months

Other

MeasureTime frame
Total cholesterol6-months
Body composition6-months

Countries

United States

Outcome results

None listed

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