- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07465094
Workplace Health Promotion "So Healthy, Lose 99" Weight Loss Activity
Obesity has become one of the global health problems. According to the World Health Organization, obesity not only affects an individual's physical health, but also increases the risk of multiple chronic diseases, cardiovascular and metabolic health problems.
According to the health examination results of all hospital employees, there are many people with high body mass index. In order to increase employees' emphasis on health management, we held a weight loss competition to evaluate the effectiveness of So99 App. We hope to create a healthy workplace culture and reduce obesity-related risks through healthy eating, regular exercise and teamwork.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Taichung, Taiwan, 407
- China Medical University Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Employees of China Medical University Hospital
- Aged 20 to 64
- Body Mass Index (BMI) ≥ 27 (kg/ m²)
Exclusion Criteria:
- Pregnant women or those planning to become pregnant
- Individuals with a history of liver or kidney dysfunction, cardiovascular disease, stroke, or cancer
- Individuals before or after major surgery
- Individuals with severe mental or neurological disorders
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: So99 group: Use the So99 app for daily health records and app activities
|
Use the So99 app for daily health records and app activities
|
|
No Intervention: 94So group
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Percent (%) change from baseline in body weight
Time Frame: 12 weeks
|
12 weeks
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CMUH114-REC1-033
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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