Efficacy of a Combined Ergonomic Health Promotion Intervention on Employee Health

Not Applicable

Completed

Interventions: Behavioral: Ergonomic Intervention
Behavioral: Active Workstation Intervention
Behavioral: Email Intervention
Device: Bluetooth enabled device (Wahoo Fitness Blue SC sensor) and accompanying iPod application.

Brief Summary: Our objective in this pilot study is to test the combined effect of a) replacing office workers' sedentary workstations with active workstations (LifeBalance Station) and b) optimizing computer workstation ergonomics on daily occupational sedentary time, cardiometabolic risk factors, musculoskeletal symptom health outcomes and work productivity.

Detailed Description: Primary Aim: To compare the effects of providing sedentary employees with seated active workstations in combination with an ergonomic intervention and regular motivational emails (experimental group) against the ergonomic intervention and regular emails only (active control group) on occupational sedentary behavior over 16 weeks.

Hypothesis: The addition of a seated active workstation will result in significant reductions in daily occupational sedentary time compared to the active control group.

Secondary Aims: To compare the effects of the experimental group against the active control group on secondary measures of cardiometabolic disease risk factors, musculoskeletal discomfort, cognitive function and work productivity.

Hypothesis 1: The experimental group will result in reduced cardiometabolic disease risk, musculoskeletal discomfort and work limitations compared to the active control group.

Recruitment & Eligibility

Inclusion Criteria

We will recruit overweight/obese (body mass index 25.0-40.0 kg/m2) adults (18-65 years) working in full-time (minimum 35 hours/week), sedentary (self-report sitting >75% work time) occupations at an independent work site.

Exclusion Criteria

Working in an office that will not meet the space or electrical requirements of the active workstation, acute or chronic illness not under treatment of a provider, orthopedic limitations that prohibit physical activity, current or planned pregnancy, hospitalization from a physical or mental disorder in the past six months and/or taking medication that may impair physical activity

Arm && Interventions

Group	Intervention	Description
Active Control	Ergonomic Intervention	This group will receive the ergonomic intervention and email intervention only for 16 weeks. This group will not receive a seated active workstation.
Experimental Group	Bluetooth enabled device (Wahoo Fitness Blue SC sensor) and accompanying iPod application.	This group will receive the seated active workstation intervention, the ergonomic intervention and the email intervention for 16 weeks.
Experimental Group	Email Intervention	This group will receive the seated active workstation intervention, the ergonomic intervention and the email intervention for 16 weeks.
Active Control	Email Intervention	This group will receive the ergonomic intervention and email intervention only for 16 weeks. This group will not receive a seated active workstation.
Experimental Group	Active Workstation Intervention	This group will receive the seated active workstation intervention, the ergonomic intervention and the email intervention for 16 weeks.
Experimental Group	Ergonomic Intervention	This group will receive the seated active workstation intervention, the ergonomic intervention and the email intervention for 16 weeks.
Active Control	Bluetooth enabled device (Wahoo Fitness Blue SC sensor) and accompanying iPod application.	This group will receive the ergonomic intervention and email intervention only for 16 weeks. This group will not receive a seated active workstation.

Primary Outcome Measures

Name	Time	Method
Change in Occupational Physical Activity From Baseline to 16 Weeks	Baseline and 16 weeks	Occupational physical activity (primary outcome) will be measured objectively with the GENEActiv physical activity monitor. The monitor will be worn on the right ankle and will be worn for 5 working days during all non-bathing hours. The outcome measure will be change in occupational activity (average counts/work day) from baseline to 16 weeks. The measure will be calculated as follows: 16 weeks value - baseline value.

Secondary Outcome Measures