Actively Recruiting
Associations Between Dietary Intake and Cardiometabolic and Gut Microbiota Outcomes in Singapore Adults
Led by National University of Singapore · Updated on 2025-05-21
240
Participants Needed
1
Research Sites
13 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to explore the connections between dietary intake, markers of cardiometabolic health, and gut microbiota composition in adults living in Singapore. It addresses the lack of studies focusing on Asian populations by considering their unique genetic, metabolic, and dietary characteristics. The goal is to better understand how diet influences health outcomes specific to this population and to contribute to improved dietary guidelines. The study is observational and cross-sectional, involving adults aged 21 to 80 years. Participants are grouped by age into younger (21-64 years) and middle-aged to older adults (65-80 years). Researchers collect detailed dietary information over seven days and measure various health markers, including blood pressure, blood lipids, fasting glucose, endothelial progenitor cell counts, and several fecal biomarkers related to gut health. Additional assessments cover sleep quality, cognitive function, skin carotenoid levels, physical activity, stress, anxiety, depression, vision, and advanced skin glycation end products. Participants will attend a study visit where blood and fecal samples are collected alongside completing questionnaires and physical assessments. Researchers evaluate primary outcomes such as dietary intake and multiple health biomarkers on the first day, while secondary outcomes include sleep, mental health, physical activity, and vision measures. The study provides valuable insights into diet’s impact on cardiometabolic and gut health and lasts from the start visit until all assessments are completed, with no treatment administered.
CONDITIONS
Brief Title
Associations Between Dietary Intake and Cardiometabolic and Gut Microbiota Outcomes
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Able to give informed consent
- Adults aged 21 to 80 years
- Able to read and understand English
- Have sufficient venous access for blood sampling as required
- No major changes in diet during the past year
- If taking antihypertensive, cholesterol-lowering, or type 2 diabetes medication, have been on it consistently for over 5 years prior to the study start
You will not qualify if you...
- Taking dietary supplements or fermented foods that may affect gut microbiota (e.g., antibiotics, prebiotics, probiotics, yogurt, kimchi) within 2 months before the first study visit
- Taking supplements or medications that may affect sleep outcomes (e.g., nutritional shakes, tryptophan, 5-hydroxytryptophan, melatonin) within 1 month before the study
- Taking supplements that may affect eye outcomes (e.g., vitamin A or vitamin A-containing multivitamins) within 2 months before the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo assessments including dietary intake, blood pressure, blood lipid profiles, fasting blood glucose, endothelial progenitor cell count, and fecal biomarkers to evaluate cardiometabolic health and gut microbiota composition.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
National University of Singapore
Singapore, Singapore, Singapore, 117546
Actively Recruiting
Research Team
Y
Yao Yueying
J
Jung Eun Kim, PhD, RD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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