Metabolic Syndrome Clinical Trial
Official title:
Effects of Low Carbohydrate Diet Compared to Low Fat Diet in Reversing the Metabolic Syndrome Using NCEP ATP III Criteria; Randomized Clinical Trial
NCT number | NCT04681924 |
Other study ID # | 6122342016 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | January 1, 2017 |
Est. completion date | July 3, 2017 |
Verified date | December 2020 |
Source | Hawler Medical University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The National Cholesterol Education Program Adult Treatment Panel-III (NCEP ATP III) definition of metabolic syndrome (MetS)is one of the most widely used criteria of metabolic syndrome. It incorporates the key features of hyperglycemia/insulin resistance, visceral obesity, dyslipidemia and hypertension. According to the NCEP ATP III guidelines, in our study, the participants having the metabolic syndrome if they possess three or more of the following criteria: abdominal obesity: Increased waist circumference, Elevated serum triglycerides, Reduced high density lipoprotein cholesterol (HDL), Elevated blood pressure both systolic blood pressure (SBP) and diastolic and Elevated fasting blood glucose. Although the pathogenesis of MetS is strongly linked to excessive food consumption, in particular fat intake, still there is no consensus about the effects of low carbohydrate diet (LCD) versus low fat diet (LFD) on reversing the MetS and on its metabolic risk factors. However, concerns have been raised with regard to the macronutrient shift with high carbohydrate restriction and the substantial intakes of fats, which may present unfavorable effects on cardiovascular disease risk factors. Meanwhile the LFD has generally been supported by studies to have beneficial effects on these risk factors. There is no consensus about the effects of LCD versus LFD on the metabolic syndrome. This study investigated the effects of LCD versus LFD on the obese peoples and followed up them for 6 months. Out of 289 obese adults apparently healthy were randomly chosen by a stratified multistage probability sampling method, 94 of them are agreed to participate in the study. They were assigned randomly into low carbohydrate and low-fat diet groups. Both groups were followed up for 6 months and the data were taken at baseline, after 3 months and 6 months of intervention. Ninety-four obese participants completed the intervention.
Status | Completed |
Enrollment | 94 |
Est. completion date | July 3, 2017 |
Est. primary completion date | June 1, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: 1. All adult obese participants 2. Had 3 or more of the following criteria of metabolic syndrome according to the NCEP ATP III guidelines: - Abdominal obesity: increased waist circumference - Elevated triglycerides - Reduced HDL - Elevated blood pressure - Elevated fasting glucose Exclusion Criteria: 1. Individuals with history or diagnosed with diseases and health related issues like: - Diabetes mellitus - Hypertension - Chronic skin disease - Heart disease - Hyperlipidemia - Malignant disease - Rheumatoid arthritis 2. Those who had undergone surgery during one month before the study |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Hawler Medical University |
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Prevalence of metabolic syndrome | The number of participants in the sample with the criteria of metabolic syndrome, divided by the total number of participants in the sample.
According to the NCEP ATP III guidelines, the participants having the metabolic syndrome if they possess three or more of the following criteria: Abdominal obesity, elevated triglycerides, reduced HDL, elevated blood pressure and elevated fasting glucose. |
Baseline | |
Primary | Change from baseline in metabolic syndrome and at 6 months | Data on baseline characteristics of adult participants were expressed as means ± SD and/ or frequencies and percentage. The data checked for normal distribution by Shapiro-Wilk test; the p-value was 0.10 which indicates that the data was normally distributed. The study used t tests and Chi square test of association to compare baseline characteristics between both diet programs. An independent samples t-test was used to compare the means of a normally distributed metabolic risk factors for both independent diet programs at the baseline and after 6 months of intervention. | 6 months | |
Primary | Compare prevalence of metabolic syndrome in both diet programs | A two-way repeated measures ANOVA was used to compare differences of metabolic dependent variables between the two independent variables, the LCD & LFD, at baseline, after 3 months and after 6 months. To determine how much of an effect of intervention has had on the participants, the study used the following cut-offs to interpret the results: 0.14 or more are large effects, 0.06 are medium effects and 0.01 are small effects. | 6 months | |
Secondary | Body mass index | The formula used for calculating body mass index (BMI) was as following: BMI=weight(kg)/height(m2) | Baseline | |
Secondary | Change from baseline in abdominal obesity and at 6 months | Waist circumference in cm was measured midway above umbilical. Abdominal obesity by increased waist circumference (in men: >= 102 cm while in women: >= 88 cm). | 6 months | |
Secondary | Change from baseline in elevated triglycerides and at 6 months | Blood samples for lipid profile as as mg/ dL were obtained after participants fasted overnight (8-10 hours). The serum analyzed by the(BIOTECNICA BT4500 Full Automated Chemistry Analyser, 2016). Elevated triglycerides if it was >= 150 mg/dL). | 6 months | |
Secondary | Change from baseline in reduced HDL and at 6 months | Blood samples for lipid profile as as mg/ dL were obtained after participants fasted overnight (8-10 hours). The serum analyzed by the(BIOTECNICA BT4500 Full Automated Chemistry Analyser, 2016). Reduced HDL if it was in men: < 40 mg/dL while in women: < 50 mg/dL). | 6 months | |
Secondary | Change from baseline in elevated blood pressure and at 6 months | Blood pressure as mmHg was measured using an MDF Desk Mercury Sphygmomanometer (Model No:MDF 800). elevated blood pressure if it was >= 130/85 mm Hg. | 6 months | |
Secondary | Change from baseline in elevated fasting glucose and at 6 months | Blood samples for blood glucose as as mg/ dL were obtained after participants fasted overnight (8-10 hours). The serum analyzed by the(BIOTECNICA BT4500 Full Automated Chemistry Analyser, 2016).Elevated fasting glucose if it was >= 100 mg/dL. | 6 months |
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