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Glycaemic Control Effect of BSG and Underlying Gut - Related Mechanism in Singapore Adults With Metabolic Syndrome

Not Applicable
Active, not recruiting
Conditions
Diabetes
Metabolic Syndrome
Interventions
Dietary Supplement: autoclaved BSG-containing biscuits
Dietary Supplement: control biscuits
Dietary Supplement: bio-transformed BSG-containing biscuits
Registration Number
NCT05529108
Lead Sponsor
National University of Singapore
Brief Summary

The purpose of this research project is to assess the glycaemic controlling effects of consuming BSG and bio-transformed BSG-containing biscuits and its underlying gut - related mechanism in adults with MetS using in-vivo setting.

Detailed Description

This is a double-blind, randomised, parallel experiment, all subjects (38 adults in Singapore with MetS) will complete a 12-week intervention period. Subjects will be randomly assigned to consume their habitual diet with biscuit that either does not contain or contains autoclaved BSG or bio-transformed BSG for 12 weeks. Throughout the intervention, subjects will be assessed for glucose, insulin, lipid and amino acid responses, biomarkers of gut health, and as well as other markers of health.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
38
Inclusion Criteria
  • Male and female participants, aged 35-85 years old
  • English-literate and able to give informed consent in English
  • Willing to follow the study procedures
  • Meet any 3 of the 5 following NCEP-ATP III MetS criteria: waist circumference > 102 cm (male), > 88 cm (female) (For Asian population: Waist circumference > 90 cm (male), > 80 cm (female)); fasting glucose concentration ≥ 100 mg/dL or on medication; triglyceride ≥ 150 mg/dL or on medication; high density lipoprotein cholesterol (HDL) < 40 mg/dL (male), < 50 mg/dL (female); systolic or diastolic blood pressure > 130/85 mmHg or on medication);
Exclusion Criteria
  • Significant change in weight (≥ 3 kg body weight) during the past 3 months
  • Allergy to barley, wheat, corn, egg, or other ingredients found inside the biscuits.
  • Acute illness at the study baseline
  • Exercising vigorously* over the past 3 months. *Defined as having > 6 metabolic equivalents of exercise daily; approximately 20 mins of moderate intensity exercise (e.g. slow jogging) a day
  • Following any restricted diet (e.g. vegetarian)
  • Smoking
  • Have a daily intake of more than 2 alcoholic drinks per day
  • Taking dietary supplements or food which may impact the outcome of interests (e.g. fermented foods, probiotic supplement etc.)
  • Consumption of antibiotics over past 3 months.
  • Pregnant, lactating, or planning pregnancy in the next 6 months
  • Insufficient venous access to allow the blood collection
  • Prescribed and taking antihypertensive/cholesterol-lowering/ type-2 diabetic medication which started less than 3 years prior to the intervention participation
  • High current intake of fibre* from brown rice or wholemeal products. *High, moderate or low intake taken as ≥ 6 servings, 4 - 5 servings, and ≤ 3 servings daily respectively based on My Healthy Plate guidelines
  • High current intake of fibre* from vegetables. * High, moderate or low intake taken as ≥ 2 servings, 2 servings, and ≤ 1 serving respectively based on My Healthy Plate guidelines

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
autoclaved BSG-containing groupautoclaved BSG-containing biscuitsSubjects are required to consume 90 g autoclaved BSG-containing biscuits as their breakfast everyday during 12-week intervention period.
Control biscuits groupcontrol biscuitsSubjects are required to consume 90 g control biscuits as their breakfast everyday during 12-week intervention period.
bio-transformed BSG-containing groupbio-transformed BSG-containing biscuitsSubjects are required to consume 90 g fermented BSG-containing biscuits as their breakfast everyday during 12-week intervention period.
Primary Outcome Measures
NameTimeMethod
Change in insulin concentrationEvery 12 week (week 0 and week 12)

Insulin concentration in the blood will be measured

Change in blood glucose concentrationEvery 12 week (week 0 and week 12)

Glucose concentration in the blood will be measured

Change in blood triglyceride concentrationEvery 12 week (week 0 and week 12)

Triglyceride concentration in the blood will be measured

Change in blood cholesterol concentrationEvery 12 week (week 0 and week 12)

Total cholesterol concentration in the blood will be measured

Change in blood Low-density Lipoprotein-cholesterol (LDL) concentrationEvery 12 week (week 0 and week 12)

Low-density Lipoprotein-cholesterol concentration in the blood will be measured

Change in High-density Lipoprotein-cholesterol (HDL) concentrationEvery 12 week (week 0 and week 12)

High-density Lipoprotein-cholesterol concentration in the blood will be measured

Change in Hemoglobin A1c (HbA1c) concentrationEvery 12 week (week 0 and week 12)

Hemoglobin A1c (HbA1c) concentration in the blood will be measured

Change in IL-6 concentrationEvery 12 week (week 0 and week 12)

IL-6 concentration in the blood will be measured

Change in TNF-alpha concentrationEvery 12 week (week 0 and week 12)

TNF-alpha concentration in the blood will be measured

Change in C-reactive protein concentrationEvery 12 week (week 0 and week 12)

C-reactive protein concentration in the blood will be measured

Change in gut microbiome compositionEvery 12 week (week 0 and week 12)

Gut microbiome composition in the fecal will be measured

Change in short chain fatty acids concentrationEvery 12 week (week 0 and week 12)

Short chain fatty acids concentration in the fecal will be measured

Change in bile acid concentrationEvery 12 week (week 0 and week 12)

Bile acid concentration in the fecal will be measured

Secondary Outcome Measures
NameTimeMethod
Change in blood pressureEvery 4 week (week 0, week 4, week 8 and week 12)

Systolic and diastolic blood pressure (in mmHg) will be measured by a blood pressure monitor.

Change in zonulin concentrationEvery 12 week (week 0 and week 12)

Zonulin concentration in the fecal will be measured

Change in calprotectin levelsEvery 12 week (week 0 and week 12)

Calprotectin concentration in the fecal will be measured

Change in sleep quality by questionnaireEvery 4 week (week 0, week 4, week 8 and week 12)

Questionnaire will be used to assess sleep quality

Change in appetite assessed by visual analogue scaleEvery 4 week (week 0, week 4, week 8 and week 12)

Visual analogue scale will be used to assess appetite.

Change in weight and heightEvery 4 week (week 0, week 4, week 8 and week 12)

Weight (in kilograms) and height (in meters) will be combined to report BMI in kg/m\^2

Change in skin advanced glycation end products statusEvery 4 week (week 0, week 4, week 8 and week 12)

Skin advanced glycation end products status will be measured by a monitor.

Change in dietaryEvery 4 week (week 0, week 4, week 8 and week 12)

Questionnaire will be used to record dietary

Trial Locations

Locations (1)

NUS Department of Food Science & Technology

🇸🇬

Singapore, Singapore

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