NCT Number: NCT03311802
A Risk Scores for Predicting Prevalence of Diabetes in the LAO Population
This was a cross-sectional investigation conducted from December 2015 to July 2017, in 15 selected rural villages of 2 districts of Vientiane municipality, Lao PDR. Target population was interested people, both men and women of age range between 30 to 70 years, living in the selected community. Someone diagnosed with diabetes and/or using any anti-diabetic drug was excluded.
The study protocol initiated with the interview on demographic and behavior information with each participant, followed by physical exam and blood pressure measurement.
Fasting glucose were measured.
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About this study
All participants were invited to meet with the researcher.
Demographic data comprises of age, gender, family history of diabetes including parents and sibling, female with history of having baby weighing more than 4 kg, gestational diabetes, and history or current of dyslipidemia (triglycerides >150 mg/dl, LDL-C ≥ 100 mg/dl, HDL-c < 35 mg/dl), and behavior data were smoking habit, physical inactivity (less than 150 min/week or 3 day/week) were collected by interview.
After that each participant was appointed for blood pressure measurement. Body mass index was computed from body weight (kg) divided by body height (m2) using the weight and height scale.
Waist Circumference was measured at the midpoint between the superior border of iliac crest and the lowest rib using measuring tape with the subject in the position of standing relax and in underclothes
Hip circumference is measured at the level of maximal gluteal protrusion
Blood pressure (BP) value was done with the participants, after 5 minutes relaxing, sitting up right with their upper arm positioned at heart level and measured by Omron blood pressure monitor.
Fasting Plasma Glucose was utilized to identify an individual who is normal, has either pre-diabetes or undiagnosed diabetes. Venous blood samples were collected 5 ml from antecubital vein into the test tube
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- of age range between 30 to 70 years, living in the selected community.
Exclusion criteria
- diagnosed with diabetes and/or using any anti-diabetic drug
Treatment and study plan
Primary outcomes
-
fasting plasma glucose
Time frame: 06.00-09.00 am
overnight fasting blood glucose
Sponsors and collaborators
Lead sponsor
Chulalongkorn University
Other
Registry information
Important dates
- Study start
- 2015
- Primary completion
- 2016
- Study completion
- 2017
- First posted
- Oct 17, 2017
- Registry last updated
- Oct 17, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.