- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02206113
Sit to Stand Intervention for Allina Health Employees
January 26, 2015 updated by: Allina Health System
A Sit-to-Stand Intervention for Allina Health Employees: A Pilot Study
A 16 week pilot study for Allina call center employees to look at the psychological outcomes and biological markers after an intervention of using a standing work station.
There were two groups: group 1 received, and was instructed to use, the standing work station for all 16 weeks, group 2 was a wait-list control group and received, and was instructed to use, the standing work station for the second 8 weeks.
Psychological outcomes were measured at weeks 0, 4, 8, 12, and 16.
Biological markers were measured at weeks 0, 8, and 16.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
39
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
-
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Minnesota
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Minneapolis, Minnesota, United States, 55407
- Allina Health
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-
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 to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Allina Health Call Center Employee (75% or higher employee status)
- Aged 18 to 65 years
- Provide written informed consent
Exclusion Criteria:
- Unable to stand for 20 minutes continuously unaided
- Home based employees
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
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 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.
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Other Names:
|
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Active Comparator: 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.
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Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in self-reported quality of life
Time Frame: Baseline, week 4, week 8, week 12, week 16
|
Change in quality of life will be measured through the administration of the PROMIS-29 questionnaire.
|
Baseline, week 4, week 8, week 12, week 16
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in waist circumference
Time Frame: Baseline, Week 8, Week 16
|
Waist circumference measured in inches
|
Baseline, Week 8, Week 16
|
|
Change in number of minutes stood per day
Time Frame: Baseline, week 8, week 16
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Participants recorded their number of minutes stood at work daily from baseline through week 16.
|
Baseline, week 8, week 16
|
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Change in self-reported stress
Time Frame: Baseline, week 4, week 8, week 12, week 16
|
Change in stress will be measured through the administration of the Perceived Stress Scale (PSS).
|
Baseline, week 4, week 8, week 12, week 16
|
|
Change in health promotion and lifestyle choices
Time Frame: Baseline, week 4, week 8, week 12, week 16
|
Change in health promotion and lifestyle choices will be measured through the administration of the Health Promoting Lifestyle Profile Questionnaire (HPLP-II).
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Baseline, week 4, week 8, week 12, week 16
|
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Change in workplace productivity
Time Frame: Baseline, week 4, week 8, week 12, week 16
|
Change in workplace productivity will be measured through the administration of Workplace Productivity and Activity Impairment (WPAI) questionnaire.
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Baseline, week 4, week 8, week 12, week 16
|
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Change in self-reported physical activity levels
Time Frame: Baseline, week 4, week 8, week 12, week 16
|
Change in self-reported physical activity levels will be measured through the administration of the International Physical Activity Questionnaire (IPAQ)
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Baseline, week 4, week 8, week 12, week 16
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Change in Body Mass Index (BMI)
Time Frame: Baseline, Week 8, Week 16
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Change in an individual's BMI after being weighed at baseline, week 8, and week 16.
|
Baseline, Week 8, Week 16
|
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Change in body fat percentage
Time Frame: Baseline, week 8, week 16
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Change in body fat percentage as measured by a BodPod® Assessment.
|
Baseline, week 8, week 16
|
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Change in resting heart rate
Time Frame: Baseline, week 8, week 16
|
Change in resting heart rate from baseline to week 16.
|
Baseline, week 8, week 16
|
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Change in blood pressure (systolic and diastolic)
Time Frame: Baseline, week 8, week 16
|
Change in both systolic and diastolic blood pressure from baseline to week 16.
|
Baseline, week 8, week 16
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jeffery Dusek, PhD, Allina Health
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
May 1, 2013
Primary Completion (Actual)
November 1, 2013
Study Completion (Actual)
November 1, 2013
Study Registration Dates
First Submitted
July 28, 2014
First Submitted That Met QC Criteria
July 31, 2014
First Posted (Estimate)
August 1, 2014
Study Record Updates
Last Update Posted (Estimate)
January 28, 2015
Last Update Submitted That Met QC Criteria
January 26, 2015
Last Verified
January 1, 2015
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 3989-1
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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