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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04392882
Other study ID # Legumes_Weight Reduction
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2011
Est. completion date March 31, 2013

Study information

Verified date January 2021
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a 12-week, randomized nutritional intervention study to determine the effect of legumes consumption on body weight in obese subjects.


Recruitment information / eligibility

Status Completed
Enrollment 400
Est. completion date March 31, 2013
Est. primary completion date March 31, 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria: 1. Male and female volunteers between the ages of 20 to 70 years 2. Body mass index (BMI) of 25 kg/m2 or higher (based on Asia-Pacific guideline) 3. Volunteers who have agreed to participate in the study and provided a written content by him/herself Exclusion Criteria: 1. Those with type 2 diabetes, cardiovascular disease, psychiatric problems, thyroid disorders, liver or kidney disease 2. Those under the use of any medications (antihypertensive, lipid-lowering, antiplatelet, antidiabetic, etc.).

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Legume enriched diet group
Replacing 1/3 refined rice intake with legumes three times per day Vegetable intake at least six units (30-70 g/unit) per day for sufficient dietary fiber intake Regular 30-min walk after dinner each day

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Outcome

Type Measure Description Time frame Safety issue
Primary Changes of BMI Changes of weight in kilograms was assessed before and after the intervention.
Changes of height in meters was assessed before and after the intervention.
Weight and height were combined to report BMI in kg/m^2.
12 weeks
Primary Changes of Insulin Resistance (IR) Changes of fasting serum glucose in mmol/L was assessed before and after the intervention.
Changes of fasting insulin in µIU/mL was assessed before and after the intervention.
Fasting insulin and fasting glucose were combined to report IR using the following equation: homeostasis model assessment (HOMA)-IR=[fasting insulin (µIU/mL)×fasting glucose (mmol/L)] /22.5.
12 weeks
Primary Changes of lipid profiles Triglyceride in mg/dL was assessed before and after the intervention.
Total-cholesterol in mg/dL was assessed before and after the intervention.
HDL-cholesterol in mg/dL was assessed before and after the intervention.
LDL-cholesterol was indirectly estimated using the friedewald formula: LDL-cholesterol= total-cholesterol-[HDL-cholesterol+(triglycerides/5)].
12 weeks
Primary Changes of serum high C-reactive Changes of serum high C-reactive in mg/L was assessed before and after the intervention. 12 weeks
Primary Changes of urinary 8-epi-PGF2a Changes of urinary 8-epi-PGF2a in pg/mg creatinine was assessed before and after the intervention. 12 weeks
Primary Changes of adiponectin Changes of adiponectin in ng/mL was assessed before and after the intervention. 12 weeks
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