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A Nutrition Education Module to Modify Sugar Consumptions Among Individuals With Cardio Metabolic Risks

NCT05746000 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2023-02-27

No results posted yet for this study

Summary

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.

Conditions

  • Cardiometabolic Syndrome

Interventions

BEHAVIORAL

Intervention Group (IG)

Three individual diet counselling that includes sugar calculation (sugar exchange) (60 minutes per session) at baseline, week-4 and week-8.

BEHAVIORAL

Control Group (CG)

Three individual diet counselling (60 minutes per session) at baseline, week-4 and week-8.

Sponsors & Collaborators

  • Universiti Putra Malaysia

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-04-01
Primary Completion
2023-12-31
Completion
2023-12-31

Countries

  • Malaysia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05746000 on ClinicalTrials.gov