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

Kansas State University

Status: Unknown

Conditions: Hypertension; Cholesterolemia; Obesity; Mood; Behavior, Health; Glucose, High Blood; Fatigue; Stress; Sedentary Behavior

Treatments: Behavioral: Program Only; Device: Desk Only

Study type: Interventional

Funder types: Other

Identifiers

NCT04641689

IRB8886

Details and patient eligibility

About

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.

Full 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.

Enrollment: 100 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts 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

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Factorial Assignment

Masking: None (Open label)

---

100 participants in 4 patient groups

Desk Only

Active Comparator group

Description:

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

Treatment:

Device: Desk Only

Program Only

Active Comparator group

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.

Treatment:

Behavioral: Program Only

Desk + Program

Experimental group

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.

Treatment:

Device: Desk Only

Behavioral: Program Only

Waitlist Control

No Intervention group

Description:

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