Development of Workplace Physical Activity Promotion Models in Taiwan
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Anticipated)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Contact
Study Contact
- Name: Meng-Yueh Chien, Doctor
- Phone Number: +886-2-33668141
- Email: mychien@ntu.edu.tw
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
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / 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
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
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
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: Meng-Yueh Chien, National Taiwan University Hospital
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (Anticipated)
Primary Completion
Study Completion (Anticipated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Estimate)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
Other Study ID Numbers
- 201310041RINA
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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