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Stand Up Kansas: An Intervention to Reduce Sedentary Behavior in the Home Work Environment

Primary Purpose

Sedentary Behavior, Behavior, Health, Cholesterolemia

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Desk Only
Program Only
Sponsored by
Kansas State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Sedentary Behavior focused on measuring physical activity

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Full-time employee (works >30 hours per week)
  • Sedentary job (>75% of workday seated)
  • Working primarily at home (>80% of typical week)
  • Able to safely engage in light intensity physical activity
  • No ambulatory limitations

Exclusion Criteria:

  • Working <30 hours per week
  • Standing or physically active >25% of typical workday
  • Working on campus >20% of a typical week OR planning to resume work on campus in the next 3 months
  • Uncontrolled stage 2 (severe) hypertension without a medical release signed by a physician

Sites / Locations

  • Kansas State University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Experimental

No Intervention

Arm Label

Desk Only

Program Only

Desk + Program

Waitlist Control

Arm Description

Participants will receive a height-adjustable desk to use in their home work environment.

Participants will receive 12 weeks of online content to support reductions in sedentary behavior while working from home. Content will be based on social cognitive theory.

Participants will receive a height-adjustable desk to use in their home work environment AND 12 weeks of online content to support reductions in sedentary behavior while working from home.

Participants will receive the intervention (desk + program) after all follow-up data have been collected.

Outcomes

Primary Outcome Measures

Change in sedentary behavior during the workday
Measured via 5-day activity log

Secondary Outcome Measures

Change in physical activity
International Physical Activity Questionnaire (long form)
Changes in sitting, standing and stepping
activPAL (subsample)
Change in productivity
Health and Work Questionnaire
Change in stress
Perceived Stress Scale (4-item)
Change in fatigue
Fatigue Symptom Inventory
Change in mood
Positive and Negative Affect Schedule
Change in diet
Rapid Eating Assessment for Participants - Shortened Version
Change in blood pressure
Measured using automatic blood pressure cuff
Change in fasting blood glucose
Blood sample obtained via finger stick
Change in cholesterol
Total, HDL, and LDL; Blood sample obtained via finger stick
Change in triglycerides
Blood sample obtained via finger stick
Change in waist circumference
Measured to the nearest 0.5 cm
Change in weight
Measured in kg

Full Information

First Posted
November 18, 2020
Last Updated
November 18, 2020
Sponsor
Kansas State University
Collaborators
University of Kansas Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT04641689
Brief Title
Stand Up Kansas: An Intervention to Reduce Sedentary Behavior in the Home Work Environment
Official Title
Stand Up Kansas: An Intervention to Reduce Sedentary Behavior in the Workplace
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
October 21, 2020 (Actual)
Primary Completion Date
March 2021 (Anticipated)
Study Completion Date
July 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kansas State University
Collaborators
University of Kansas Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This project will examine the effectiveness of an intervention to reduce sedentary behavior in Kansas State University employees who are primarily working from home. We will recruit 100 employees to participate. Participants will be randomly assigned to one of four conditions: desk only, program only, desk + program, or waitlist control. The program will consist of strategies to reduce sitting and increase physical activity in the home environment. We will assess whether the intervention successfully elicits reductions in sitting among employees, as well as changes in cardiometabolic and work-related outcomes.
Detailed Description
For this project we will conduct a 12-week intervention that incorporates multiple strategies to reduce sedentary behavior among university employees who are primarily working from home. Participants will be recruited via campus networks. Participants will attend an initial testing visit, during which anthropometric and health outcome data (blood pressure, blood glucose and cholesterol) will be collected. Following the testing visit, all participants will complete an activity log for the next 5 work days, and a subsample will wear an activPAL 4 device for 7 days. All participants will complete a series of questionnaires (measuring physical activity, fatigue, stress, productivity, mood, and diet) online. After all baseline data have been collected, participants will be randomized to one of four conditions: desk only, program only, desk + program, or waitlist control. Those in the desk only and desk+program conditions will receive a height-adjustable desk. They will be asked to set up the desk at their home workstation and send a photo of the setup to our research team within one week. Those in the program only and control conditions will receive their height-adjustable desks after completing the post-intervention assessments. Participants assigned to the program only and desk+program conditions will have access to a website that includes a variety of resources for reducing sedentary behavior and increasing physical activity in the home environment. The intervention program will be based on social cognitive theory and will be designed to promote self-efficacy, self-regulation, positive outcome expectations, and social and environmental support. Participants will complete weekly modules that include activities such as goal setting and self-monitoring, action and coping planning, group discussions, etc. The program will also provide suggestions for changes to the home work environment, access to virtual stretching and strengthening videos, examples of technology to prompt breaks, etc. Participants will also receive 2 small group coaching calls via Zoom (at 3 and 8 weeks) to assist them in setting goals for reducing sedentary behavior and overcoming barriers. Participants in the desk only and waitlist control groups will receive access to the program after completing the post-intervention assessments. All measures will be repeated following the 12-week intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sedentary Behavior, Behavior, Health, Cholesterolemia, Obesity, Stress, Hypertension, Fatigue, Glucose, High Blood, Mood
Keywords
physical activity

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Model Description
2 x 2
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Desk Only
Arm Type
Active Comparator
Arm Description
Participants will receive a height-adjustable desk to use in their home work environment.
Arm Title
Program Only
Arm Type
Active Comparator
Arm Description
Participants will receive 12 weeks of online content to support reductions in sedentary behavior while working from home. Content will be based on social cognitive theory.
Arm Title
Desk + Program
Arm Type
Experimental
Arm Description
Participants will receive a height-adjustable desk to use in their home work environment AND 12 weeks of online content to support reductions in sedentary behavior while working from home.
Arm Title
Waitlist Control
Arm Type
No Intervention
Arm Description
Participants will receive the intervention (desk + program) after all follow-up data have been collected.
Intervention Type
Device
Intervention Name(s)
Desk Only
Other Intervention Name(s)
VariDesk Pro Plus 36 height-adjustable desk
Intervention Description
Provision of height-adjustable desk
Intervention Type
Behavioral
Intervention Name(s)
Program Only
Intervention Description
Online modules will promote goal setting, self-monitoring, habit formation, social support, barrier identification, and environmental modifications
Primary Outcome Measure Information:
Title
Change in sedentary behavior during the workday
Description
Measured via 5-day activity log
Time Frame
Baseline and 12 weeks
Secondary Outcome Measure Information:
Title
Change in physical activity
Description
International Physical Activity Questionnaire (long form)
Time Frame
Baseline and 12 weeks
Title
Changes in sitting, standing and stepping
Description
activPAL (subsample)
Time Frame
Baseline and 12 weeks
Title
Change in productivity
Description
Health and Work Questionnaire
Time Frame
Baseline and 12 weeks
Title
Change in stress
Description
Perceived Stress Scale (4-item)
Time Frame
Baseline and 12 weeks
Title
Change in fatigue
Description
Fatigue Symptom Inventory
Time Frame
Baseline and 12 weeks
Title
Change in mood
Description
Positive and Negative Affect Schedule
Time Frame
Baseline and 12 weeks
Title
Change in diet
Description
Rapid Eating Assessment for Participants - Shortened Version
Time Frame
Baseline and 12 weeks
Title
Change in blood pressure
Description
Measured using automatic blood pressure cuff
Time Frame
Baseline and 12 weeks
Title
Change in fasting blood glucose
Description
Blood sample obtained via finger stick
Time Frame
Baseline and 12 weeks
Title
Change in cholesterol
Description
Total, HDL, and LDL; Blood sample obtained via finger stick
Time Frame
Baseline and 12 weeks
Title
Change in triglycerides
Description
Blood sample obtained via finger stick
Time Frame
Baseline and 12 weeks
Title
Change in waist circumference
Description
Measured to the nearest 0.5 cm
Time Frame
Baseline and 12 weeks
Title
Change in weight
Description
Measured in kg
Time Frame
Baseline and 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Full-time employee (works >30 hours per week) Sedentary job (>75% of workday seated) Working primarily at home (>80% of typical week) Able to safely engage in light intensity physical activity No ambulatory limitations Exclusion Criteria: Working <30 hours per week Standing or physically active >25% of typical workday Working on campus >20% of a typical week OR planning to resume work on campus in the next 3 months Uncontrolled stage 2 (severe) hypertension without a medical release signed by a physician
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emily L Mailey, PhD
Organizational Affiliation
Kansas State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kansas State University
City
Manhattan
State/Province
Kansas
ZIP/Postal Code
66506
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Stand Up Kansas: An Intervention to Reduce Sedentary Behavior in the Home Work Environment

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