- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05727592
An Intervention Study on the Effect of Brazilian Spinach Supplementation on Health Outcomes Among Type 2 Diabetes Patients in Hospital Universiti Sains Malaysia
Effectiveness Of 12-Weeks Brazilian Spinach on Health Outcomes Among Type 2 Diabetes Patients in Hospital Universiti Sains Malaysia
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Background: Vegetables are valuable health promotion foods because they contain vital nutrients such as vitamins, minerals, proteins, fibres and bio-functional components but are low in fat, sodium and calories as compared with many other foods. In terms of body fat, increase vegetable intake that consist of dietary fibre can play an important role in the regulation of body weight. Therefore, the supplementation of dietary fibre intake from vegetable may have benefit in reducing the percentages of body fat. Though, the clinical effect in human remains unclear and currently no study conducted in Malaysia regarding the effectiveness of this plant towards blood sugar control. Apart from that, lower intake of vegetable among Malaysian, lower cost vegetable choices and higher availability of Althernanthera Sissoo (Brazilian Spinach) due to easy growth may benefit the diabetes patient. Therefore, the investigators plan to conduct this study to determine the effectiveness of 12-weeks Brazilian Spinach supplementation on health outcomes among patients with type 2 diabetes especially in Kelantan region. The investigators hypothesized that diabetes patients on supplementation of Brazilian Spinach would have significant differ in terms of anthropometry, biochemical, clinical, and dietary intake compared to control group.
Method: A single-center randomized, controlled, and two-arm parallel design clinical trial will be carried out in Malaysia especially in Kelantan region. This study enrols 100 patients from Hospital Universiti Sains Malaysia (HUSM) diagnosed with type 2 diabetes. Diabetic patients who meet eligibility criteria will be randomly allocated to two groups, which are Brazilian Spinach treatment group and control group. Both groups will be compared on the primary and secondary outcomes at baseline, 3, 6, and 12 weeks.
Discussion: The study will provide insights into the potential beneficial effect of Brazilian Spinach in type 2 diabetic patients. In addition, the therapeutic effect of Brazilian Spinach towards type 2 diabetes will reflect as a change of metabolite profile in serum.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Kelantan
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Kubang Kerian, Kelantan, Malaysia, 16150
- Hospital Universiti Sains Malaysia
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age between 30-65 years old
- Have confirmed diagnosed with type 2 diabetes mellitus of equal or more than 6 months
- HbA1c levels equal or more than 7% (within the last 3 months of recruitment)
- On at least one oral hypoglycemic agent
- Agree not to take other herbal or nutritional supplements for the duration of study.
Exclusion Criteria:
- Unable to tolerate to fiber especially vegetables
- Type 1 diabetes mellitus
- Pregnant
- Insulin treatment
- Severe diabetic complications including end-stage renal diseases, liver diseases or gastrointestinal diseases
- On coagulant therapy (warfarin)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention Group
Intervention: Diabetic Brazilian spinach supplementation group Subjects in this group will be receiving Brazilian spinach for 12 weeks in which they must consume 15g of Brazilian spinach daily with lunch or dinner.
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15g of Althernanthera Sissoo consumed with lunch or dinner per day.
Other Names:
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Experimental: Control Group
No intervention: Diabetic control group Subjects in this group will not receive Brazilian spinach.
However, they will be receiving standard dietary counselling and educated for the same lifestyle intervention as in the intervention group.
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Dietary consultation to improve the intakes of vegetables daily
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Glycaemic control (HbA1c level)
Time Frame: 3 months
|
The outcome to be measured are the hbA1c level in which it will be measured in percentage.
|
3 months
|
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Fasting blood glucose
Time Frame: 3 months
|
The outcome to be measured are the fasting blood glucose (FBS) in which it will be measured in mmol/L.
|
3 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anthropometric measurements
Time Frame: 3 months
|
The outcome to be measured are the BMI in which the weight and height will be combined to report BMI in kg/m^2.
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3 months
|
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Blood pressure
Time Frame: 3 months
|
Both pressures, systolic and diastolic will be assessed that will be measured in millimeters of mercury (mmHg).
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3 months
|
|
Dietary Intake
Time Frame: 3 months
|
The dietary intake will be measured by conducting the 24-hours dietary recall toward the subjects.
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3 months
|
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Liver profile
Time Frame: 3 months
|
The outcome to be measured is the liver function test (LFT) which include alanine transaminase (ALT), aspartate transaminase (AST), and alkaline phosphatase (ALP).
This outcome will be measured in units per liter (U/L).
|
3 months
|
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Renal profile
Time Frame: 3 months
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The outcome to be measured is the renal function test (RFT) to get an estimate of the glomerular filtration rate (GFR), serum creatine, and to check for proteinuria (albuminuria).
|
3 months
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- USM/JEPeM/20120630
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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