- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02215239
Development of Workplace Physical Activity Promotion Models in Taiwan
March 13, 2015 updated by: National Taiwan University Hospital
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.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
Several evidences have shown that regular physical activity could benefit not only to a healthy lifestyle, but also reduce mortality rate.
However, the number of people who perform regular physical activity are still in a low proportion of world population.
In Taiwan, people are mostly inactive and have low level of physical activity at their workplaces.
Therefore, developing a healthy workplace could encourage employees to get into the habit of regular exercise, relieve stress, improve interaction of social activity and build a healthy life style.
Meanwhile, regular exercise could improve coherence, morale and higher satisfaction, productive efficiency, corporate image and competitiveness.
Previous studies have shown inconsistent effects in promoting physical activity in the workplace.
Therefore, determining the effects of comprehensive model using in interventions at workplaces is needed. .
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.
The intervention plan is to implement a cyclic or iterative process recommended by WHO.
The process includes eight steps: (1) Mobilize; (2) Assemble; (3) Assess; (4) Prioritize; (5) Plan; (6) Do; (7) Evaluate; (8) Improve.
By gaining the commitment from the highest authority in the enterprise and communicated to all workers and their representatives, we will be able to assemble a Healthy Workplace Team who will work on implementing change in the workplace.
As well as assembling the Team, it is also essential to assemble other resources that will be required, such as locations, time, budgets or working supplies, to ensure the committee has the resources necessary to do the work.
Assessments on both the present situation of the enterprise and the present situation with respect to the health of workers are required in order to set priorities among the many issues identified.
When developing a health plan, we focus on different phases of exercise and prescribe individualized physical activity program., in the mean while, the power of social learning and environmental support are critical in making a sustainable improvement in the workplace.
The details of the actions to be taken may contain educational workshop, pedometer using, setting fixed period of time for physical activities, providing excellent health and fitness improvement prize, email and text reminder about exercise information, holding outdoor physical activities on a regular time schedule for employee, and propagating internal and external resources.
Re-evaluation and modification will be performed at the end of 16-weeks intervention, and then the second year's study will be planned and designed.
In the present study, before intervention, we will require a confidential survey and health risk assessments about personal health condition base on employees will.
The assessments include basic data and medical record, level of physical activity, health-related fitness, sleep quality and daytime sleepiness, depression scale, exercise stages, self-evaluation of fitness and exercise capacity, self-efficacy in exercise, SmartIn(SI) system, and working performance evaluation.
The purpose of the study is to access the effect of implementing The WHO Healthy Workplace Framework and Model on different working types in different workplaces, by developing method that address the physical and psychosocial working environments, as well as promoting workers' health and creating health-promoting working environments, the result is expected to provide better information for the Health Promotion Administration in future policy-making.
Study Type
Interventional
Enrollment (Anticipated)
240
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Taipei, Taiwan, 115
- Recruiting
- National Taiwan University Hospital
-
Contact:
- Meng-Yueh Chien, Doctor
- Phone Number: 02-33668141
- Email: mychien@ntu.edu.tw
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Working type A & Workplace intervention
Participants: Workers tend to be seated during work hours.
Intervention: WHO Healthy Workplace Framework and Model.
Duration: 16 weeks.
|
WHO Healthy Workplace Framework and Model.
The intervention plan is to implement a cyclic or iterative process recommended by WHO.
The process includes eight steps: (1) Mobilize; (2) Assemble; (3) Assess; (4) Prioritize; (5) Plan; (6) Do; (7) Evaluate; (8) Improve.
We focus on different phases of exercise and prescribe individualized physical activity program.
|
No Intervention: Working type A & Usual care
Participants: Workers tend to be standing during work hours.
Intervention: Usual care.
Duration: 16 weeks.
|
|
Experimental: Working type B & Workplace intervention
Participants: Workers tend to be standing during work hours.
Intervention: WHO Healthy Workplace Framework and Model.
Duration: 16 weeks.
|
WHO Healthy Workplace Framework and Model.
The intervention plan is to implement a cyclic or iterative process recommended by WHO.
The process includes eight steps: (1) Mobilize; (2) Assemble; (3) Assess; (4) Prioritize; (5) Plan; (6) Do; (7) Evaluate; (8) Improve.
We focus on different phases of exercise and prescribe individualized physical activity program.
|
No Intervention: Working type B & Usual care
Participants: Workers tend to be standing during work hours.
Intervention: Usual care.
Duration: 16 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change of health-related physical fitness from baseline to 16-week
Time Frame: 16 weeks
|
Health-related physical fitness including:
|
16 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change of physical activity from baseline to 16-week
Time Frame: 16 weeks
|
Using 7-Day Physical Activity Recall questionnaire and actigraph to investigate level of physical activity in the participants
|
16 weeks
|
Change of sleep quality from baseline to 16-week
Time Frame: 16 weeks
|
Using Pittsburgh Sleep Quality Index, Epworth Sleepiness Scale, and actigraph to investigate sleep quality in the participants
|
16 weeks
|
Change of depression symptoms from baseline to 16-week
Time Frame: 16 weeks
|
Using Center for Epidemiologic Studies Depression Scale to investigate level of depression in the participants
|
16 weeks
|
Change of stress from baseline to 16-week
Time Frame: 16 weeks
|
Using SmartIn system to investigate level of psychological stress in the participants
|
16 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Meng-Yueh Chien, National Taiwan University Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2014
Primary Completion (Anticipated)
December 1, 2015
Study Completion (Anticipated)
December 1, 2015
Study Registration Dates
First Submitted
August 11, 2014
First Submitted That Met QC Criteria
August 12, 2014
First Posted (Estimate)
August 13, 2014
Study Record Updates
Last Update Posted (Estimate)
March 17, 2015
Last Update Submitted That Met QC Criteria
March 13, 2015
Last Verified
March 1, 2015
More Information
Terms related to this study
Other Study ID Numbers
- 201310041RINA
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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