Occupational Health Clinical Trial
Official title:
Development of Workplace Physical Activity Promotion Models in Taiwan
The purpose of this study is to investigate the effectiveness of intervention applying WHO Healthy Workplace Framework and Model to enhance the level of physical activity on employees. This research is an experimental intervention study recruiting two working types in four workplaces. Two working types are: (1) Working type A: Workers tend to be seated during work hours. Two telecommunications enterprises will respectively stand for the experiment group and the control group. (2) Working type B: Workers tend to be standing during work hours. Likewise, two different enterprises will respectively stand for the experiment group and the control group. Purposive sampling method will be used to select the experiment group. The intervention plan is to implement a cyclic or iterative process recommended by WHO.
Status | Recruiting |
Enrollment | 240 |
Est. completion date | December 2015 |
Est. primary completion date | December 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 20 Years to 65 Years |
Eligibility |
Inclusion criteria: - Workers tend to be seated or standing during work hours. - Basic capability to read or verbal communication in Chinese. Exclusion criteria: - No other critical diseases or unstable cardiopulmonary disease, diabetes, hypertension or neurological diseases. - No pregnancy. |
Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research
Country | Name | City | State |
---|---|---|---|
Taiwan | National Taiwan University Hospital | Taipei |
Lead Sponsor | Collaborator |
---|---|
National Taiwan University Hospital |
Taiwan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change of health-related physical fitness from baseline to 16-week | Health-related physical fitness including: body composition (body weight, height, waist and hip circumferences) flexibility (sit-to-reach, cm) muscle strength (grip strength of dominant hand, kg) muscle endurance (sit-up in one minute, times/min) cardiopulmonary endurance (stepping in three minutes, heart rate and physical exercise index) |
16 weeks | No |
Secondary | Change of physical activity from baseline to 16-week | Using 7-Day Physical Activity Recall questionnaire and actigraph to investigate level of physical activity in the participants | 16 weeks | No |
Secondary | Change of sleep quality from baseline to 16-week | Using Pittsburgh Sleep Quality Index, Epworth Sleepiness Scale, and actigraph to investigate sleep quality in the participants | 16 weeks | No |
Secondary | Change of depression symptoms from baseline to 16-week | Using Center for Epidemiologic Studies Depression Scale to investigate level of depression in the participants | 16 weeks | No |
Secondary | Change of stress from baseline to 16-week | Using SmartIn system to investigate level of psychological stress in the participants | 16 weeks | No |
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