- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05873140
Healthy Thai Project With Bangkoknoi Model: Fatless Community
The goal of this interventional study is to make people in a community realize negative effects of obesity on health, and how to tackle it by adopting a lifestyle modification for weight reduction. Adults aged 20 years old or more with obesity (BMI ≥ 25 kg/m2) or waist circumference ≥ 80 cm in women and ≥ 90 cm in men were recruited. All participants received an educational session of lifestyle modification for weight reduction on the first day of study. Participants were then assigned to either continuously receive education (video clips and infographics) via application LINE, or no further education. The main questions it aims to answer are:
- Whether or not an educational session of lifestyle modification leads to weight reduction.
- Whether or not a weight loss by a continuous education via an online application is more effective than not receiving it.
Study Overview
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Bangkok
-
Bangkoknoi, Bangkok, Thailand, 10700
- Faculty of Medicine Siriraj Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Obesity (BMI ≥ 25 kg/m2)
- Waist circumference ≥ 80 cm in women and ≥ 90 cm in men
Exclusion Criteria:
- Contraindications for bioelectrical impedance analysis
- Active cancer
- No available health data
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Study group
Continuously receiving education (video clips and infographics) via application LINE
|
Online lifestyle modification education for weight loss
|
|
No Intervention: Control group
No application LINE
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body weight change
Time Frame: 6 months after intervention
|
Body weight change
|
6 months after intervention
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Phunchai Charatcharoenwitthaya, MD, Mahidol University
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
Other Study ID Numbers
- Si 1000/2021
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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