Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
39 participants
INTERVENTIONAL
2013-05-31
2013-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
NONE
Study Groups
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Standing workstation - 16 weeks
This arm, Standing workstation - 16 weeks, received the intervention of a standing workstation for 16 weeks. For the first 8 weeks, the participants were instructed how long to stand per hour for an 8 hour shift. The second 8 weeks their use was monitored for sustainability.
Standing workstation
Standing workstation - second 8 weeks
This arm, Standing workstation - second 8 weeks, received the intervention of a standing workstation for 8 weeks of the study. For the first 8 weeks, the worked at their normal desks without an intervention. The second 8 weeks they received a standing workstation and their use was monitored.
Standing workstation
Interventions
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Standing workstation
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Aged 18 to 65 years
* Provide written informed consent
Exclusion Criteria
* Home based employees
18 Years
65 Years
ALL
Yes
Sponsors
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Allina Health System
OTHER
Responsible Party
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Principal Investigators
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Jeffery Dusek, PhD
Role: PRINCIPAL_INVESTIGATOR
Allina Health
Locations
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Allina Health
Minneapolis, Minnesota, United States
Countries
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Other Identifiers
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3989-1
Identifier Type: -
Identifier Source: org_study_id
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