Overweight, Sedentary
Conditions
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.
Interventions
BEHAVIORALActive Workstation Intervention
Participants in the experimental group will receive a seated active workstation at their work setting for 16 weeks.
BEHAVIORALErgonomic Intervention
Participants of both arms will receive a face to face ergonomic workstation optimization intervention. This consultation will take 30 minutes to complete and will be performed at the participant's actual work station.
BEHAVIORALEmail Intervention
Participants of both arms will receive three emails per week for 16 weeks. Messages will be consistent with what they hear in the ergonomic intervention (e.g., encourage taking breaks from sitting at work and adjusting posture to be in line with ergonomic principles).
DEVICEBluetooth enabled device (Wahoo Fitness Blue SC sensor) and accompanying iPod application.
Sponsors
University of Iowa
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 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. |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Experimental Group This group will receive the seated active workstation intervention, the ergonomic intervention and the email intervention for 16 weeks.
Active Workstation Intervention: Participants in the experimental group will receive a seated active workstation at their work setting for 16 weeks.
Ergonomic Intervention: Participants of both arms will receive a face to face ergonomic workstation optimization intervention. This consultation will take 30 minutes to complete and will be performed at the participant's actual work station.
Email Intervention: Participants of both arms will receive three emails per week for 16 weeks. Messages will be consistent with what they hear in the ergonomic intervention (e.g., encourage taking breaks from sitting at work and adjusting posture to be in line with ergonomic principles).
Bluetooth enabled device (Wahoo Fitness Blue SC sensor) and accompanying iPod application. | 30 |
| Active Control This group will receive the ergonomic intervention and email intervention only for 16 weeks. This group will not receive a seated active workstation.
Ergonomic Intervention: Participants of both arms will receive a face to face ergonomic workstation optimization intervention. This consultation will take 30 minutes to complete and will be performed at the participant's actual work station.
Email Intervention: Participants of both arms will receive three emails per week for 16 weeks. Messages will be consistent with what they hear in the ergonomic intervention (e.g., encourage taking breaks from sitting at work and adjusting posture to be in line with ergonomic principles).
Bluetooth enabled device (Wahoo Fitness Blue SC sensor) and accompanying iPod application. | 30 |
| Total | 60 |
Baseline characteristics
| Characteristic | Active Control | Experimental Group | Total |
|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical Between 18 and 65 years | 30 Participants | 30 Participants | 60 Participants |
| Age, Continuous | 45.0 years STANDARD_DEVIATION 10.7 | 45.2 years STANDARD_DEVIATION 10.9 | 45.1 years STANDARD_DEVIATION 10.8 |
| Region of Enrollment United States | 30 participants | 30 participants | 60 participants |
| Sex/Gender, Customized Female | 21 participants | 21 participants | 42 participants |
| Sex/Gender, Customized Male | 9 participants | 9 participants | 18 participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — |
| other Total, other adverse events | 0 / 30 | 0 / 30 |
| serious Total, serious adverse events | 0 / 30 | 0 / 30 |
Outcome results
Primary
Change in Occupational Physical Activity From Baseline to 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.
Time frame: Baseline and 16 weeks
| Arm | Measure | Value (MEAN) |
|---|---|---|
| Experimental Group | Change in Occupational Physical Activity From Baseline to 16 Weeks | 9752 Average counts/work day |
| Active Control | Change in Occupational Physical Activity From Baseline to 16 Weeks | -142 Average counts/work day |