- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04538222
Workplace Physical Activity Intervention
August 16, 2022 updated by: National Taiwan University Hospital
An Effectiveness Study of Workplace Physical Activity Intervention for Staff in a Hospital Setting
In this study, it investigates the effectiveness of workplace physical activity intervention for staff in a 100-bed hospital in Taipei City, Taiwan.
The physical activity program takes group coaching and includes aerobic exercise, muscle strength and stretching in combination with nutrition education.
The duration of the program is three months (8 sessions per month).
The subjects of the study were recruited from full-time employees working at the hospital who attend the program.
The recruited employees can take part in the program freely and chose types of activity by themselves.
This study measures body mass index, muscle strength, body fat percentage, muscle strength, body mass index, daily energy expenditure, and exercise self-efficacy as the baseline.
After 3-month program, we will evaluate the effectiveness of the program.
The result is anticipated the greater frequent attendance, the more obvious effectiveness in outcomes.
Study Overview
Detailed Description
A three-month group coaching physical activity program in combination with nutrition education was developed for full-time employees working on a 100-bed hospital in Taipei City, Taiwan.
Due to the setting that employees can take part in the program freely and chose types of activity by themselves.
So participants may have various intensity of participation.
This study aims to evaluate the effectiveness of pre- and post- 3-month workplace physical activity programs in body fat percentage, Muscle strength, body mass index, daily energy expenditure, and exercise self-efficacy.
One group pretest-posttest design was used for the study by convenience sampling technique.
Subjects were recruited from participants of the program.
The intervention consists of : (1)education on nutrition: 2 times per month for 3 months, 1 hour/time ; and (2)physical activity: a three-month group coaching program (24 sessions), including three types of exercise courses such as aerobic exercise, muscle strength and stretching.
All analyses were performed using Statistics Analysis System version 9.3 and the effects of the intervention were assessed by the paired t-test.
Multiple regression analysis was used to determine the contribution of attendances of activities and behavior change stage to effectiveness of workplace physical activity.
The level of significance was set at p < 0.05.
Study Type
Observational
Enrollment (Actual)
86
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
- National Taiwan University Hospital
-
-
新店區
-
Taipei City, 新店區, Taiwan, 231
- National Taiwan University Hospital
-
-
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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
individuals who participate hospital self-developed workplace physical activity
Description
Inclusion Criteria:
- full-time employees
- Complete the informed consent
Exclusion Criteria:
- With pacemaker
- accepted or are participating participate other weight control related research or interventional medicine
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change from Baseline Body fat percentage at 3 months
Time Frame: baseline, 3 month after intervention
|
Body fat percentage was the total mass of fat divided by total body mass, multiplied by 100.
Estimate for body fat percentage was measured by dual frequency bio-electric impedance(BIA) body composition analyzer.
|
baseline, 3 month after intervention
|
Change from Baseline Muscle strength at 3 months
Time Frame: baseline, 3 month after intervention
|
Muscle strength was assessed by hand grip strength using a grip strength dynamometer.
The grip strength dynamometer can measure range from 5 to 100 kg.
During the measurement, the subject stood upright and was asked to hold the grip with the dynamometer with the greatest strength.
Take the maximum value after two measurements.
|
baseline, 3 month after intervention
|
Change from Baseline exercise self-efficacy at 3 months
Time Frame: baseline, 3 month after intervention
|
The five-item self-efficacy questionnaire designed to measure confidence in one's ability to persist with exercising in various situations which included the following: tired, bad mood, don't have the time, on vacation, raining or snowing.
An 7-point scale was used to rate each item of self-efficacy, scores range from 5 "not at all confident" to 35 "very confident".
A score of 0 means "extremely low self-efficacy" and a score of 35 means" "extremely high self efficacy"
|
baseline, 3 month after intervention
|
Change from Baseline exercise behavior change stage at 3 months
Time Frame: baseline, 3 month after intervention
|
exercise behavior change stage
|
baseline, 3 month after intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change from Baseline body mass index at 3 months
Time Frame: baseline, 3 month after intervention
|
Body mass index (BMI) was calculated as body weight (kg) divided by the square of the body height (meter) (m2).
BMI was assessed using a body composition analyzer.
|
baseline, 3 month after intervention
|
Change from Baseline Daily energy expenditure at 3 months
Time Frame: baseline, 3 month after intervention
|
Daily energy expenditure as an estimate of total kilo-calories of energy expended per day.
Calculation from the seven-day physical activity recall questionnaire.
Subjects were asked to list total activities in each category and quantifying the time spent (hour) in each activity over a seven-day period.
Activities were classified by their energy requirements, expressed in terms of Metabolic Equivalent of Task (MET).
Sleep = 1 MET; light activity = 1.0-2.9
MET (MET level: 1.5); moderate activity = 3.0-5.0
MET (MET level: 4); hard activity =5.1-6.9
MET (MET level: 6); very hard activity = 7.0 or greater MET (MET level: 10).
Each activity's total kilo-calories of energy expended per day was calculated by the following equation: activity MET * times of having activity time(hours)*body weight(kg)/7 (day).
|
baseline, 3 month after intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (Actual)
September 7, 2020
Primary Completion (Actual)
November 13, 2020
Study Completion (Actual)
August 4, 2021
Study Registration Dates
First Submitted
August 25, 2020
First Submitted That Met QC Criteria
August 30, 2020
First Posted (Actual)
September 4, 2020
Study Record Updates
Last Update Posted (Actual)
August 18, 2022
Last Update Submitted That Met QC Criteria
August 16, 2022
Last Verified
August 1, 2020
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 202007050RIND
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Health Promotion
-
National Yang Ming UniversityCompleted
-
University of New MexicoCompleted
-
Florida State UniversityCompleted
-
Geisinger ClinicCompletedHealth Promotion | Wellness ProgramsUnited States
-
University of VictoriaCompleted
-
Oregon Research InstituteCompletedTobacco Smoking | Health PromotionUnited States
-
Erzi̇ncan Binali Yildirim Uni̇versi̇tesi̇Ataturk UniversityNot yet recruiting
-
Linnaeus UniversityEnrolling by invitation
-
The Institute for Functional MedicineFunctional Medicine Coaching AcademyCompleted
-
Utica CollegeCompleted
Clinical Trials on physical activity
-
Health Education Research Foundation (HERF)CompletedQuality of LifePakistan
-
Zohra Institute of Health SciencesCompletedPhysical Activity and StressPakistan
-
Centre Hospitalier Universitaire DijonWithdrawn
-
Fundacion para la Investigacion y Formacion en...CompletedImpaired CognitionSpain
-
Cardenal Herrera UniversityRecruiting
-
Istituti Clinici Scientifici Maugeri SpAActive, not recruiting
-
AUSL Romagna RiminiFondazione IRCCS Istituto Nazionale dei Tumori, MilanoRecruitingNon-Small Cell Lung CancerItaly
-
Fundación para la Investigación del Hospital Clínico...CompletedObesity | Severe Mental Disorder
-
Augusta UniversityNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); Kansas... and other collaboratorsCompletedMental Disorders, SevereUnited States
-
Centre Hospitalier Departemental VendeeTerminated