The goal of this feasibility study is to assess the feasibility of a nutrition education module in modifying sugar consumption among individuals with cardiometabolic risk. The main questions it aims to answer are: * Is the nutrition education (focusing on modifying sugars intake) intervention feasible to individuals with cardiometabolic risk? * Can the intervention be delivered as planned and works as intended? * What are the experiences, perspective and barriers of individuals with cardiometabolic risk when receiving the nutrition education intervention? * Is the nutrition education intervention efficient in modifying the eating behaviour including the sugar consumption among individuals with cardiometabolic risk? Participants in the Control Group and Intervention Group will attend three standard diet counselling, with additional sugar education for the Intervention Group.
Age range
18 Years – 65 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Proportion of eligible potential candidates who agree to participate in the study
Timeframe: At screening period. All subjects who agree to participate in the intervention will be determined.
Proportion of subjects in the intervention group who take up the intervention
Timeframe: At baseline of the intervention. All subjects who attend the intervention at baseline will be determined.
Proportion of subjects who withdraw from the study or are lost to follow-up
Timeframe: Three months of the intervention. All subjects who withdraw from the study or are lost to follow-up throughout the three months intervention will be determined.