Skip to content

Sit to Stand Intervention for Allina Health Employees

A Sit-to-Stand Intervention for Allina Health Employees: A Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02206113
Enrollment
39
Registered
2014-08-01
Start date
2013-05-31
Completion date
2013-11-30
Last updated
2015-01-28

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

Conditions

Stress, Quality of Life

Keywords

Standing workstation

Brief summary

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.

Interventions

Sponsors

Allina Health System
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Change in self-reported quality of lifeBaseline, week 4, week 8, week 12, week 16Change in quality of life will be measured through the administration of the PROMIS-29 questionnaire.

Secondary

MeasureTime frameDescription
Change in number of minutes stood per dayBaseline, week 8, week 16Participants recorded their number of minutes stood at work daily from baseline through week 16.
Change in self-reported stressBaseline, week 4, week 8, week 12, week 16Change in stress will be measured through the administration of the Perceived Stress Scale (PSS).
Change in health promotion and lifestyle choicesBaseline, week 4, week 8, week 12, week 16Change in health promotion and lifestyle choices will be measured through the administration of the Health Promoting Lifestyle Profile Questionnaire (HPLP-II).
Change in workplace productivityBaseline, week 4, week 8, week 12, week 16Change in workplace productivity will be measured through the administration of Workplace Productivity and Activity Impairment (WPAI) questionnaire.
Change in waist circumferenceBaseline, Week 8, Week 16Waist circumference measured in inches
Change in Body Mass Index (BMI)Baseline, Week 8, Week 16Change in an individual's BMI after being weighed at baseline, week 8, and week 16.
Change in body fat percentageBaseline, week 8, week 16Change in body fat percentage as measured by a BodPod® Assessment.
Change in resting heart rateBaseline, week 8, week 16Change in resting heart rate from baseline to week 16.
Change in blood pressure (systolic and diastolic)Baseline, week 8, week 16Change in both systolic and diastolic blood pressure from baseline to week 16.
Change in self-reported physical activity levelsBaseline, week 4, week 8, week 12, week 16Change in self-reported physical activity levels will be measured through the administration of the International Physical Activity Questionnaire (IPAQ)

Countries

United States

Outcome results

None listed

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