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Clinical Trials/NCT03014531
NCT03014531
Completed
Not Applicable

Daily Almond Intake as a Preload Before Meals Versus as a Snack Between Meals Has Different Effects on Body Fat Percentages and the Lipid Profile in a Randomized Controlled Trial of Young Adults in South Korea

ICAN Nutrition Education and Research1 site in 1 country227 target enrollmentStarted: June 2014Last updated:

Overview

Phase
Not Applicable
Status
Completed
Sponsor
ICAN Nutrition Education and Research
Enrollment
227
Locations
1
Primary Endpoint
Changes of body fat percentages from baseline

Overview

Brief Summary

The study was conducted to investigate the effects of daily almond intake based on the timing of almond consumption (i.e., almond consumption as a preload or between-meal snack) on body composition, lipid profile, and oxidative and inflammation indicators among young Korean adults.

Detailed Description

The current study was conducted to investigate the effects of daily almond intake on body composition, lipid profile, and oxidative and inflammation indicators among young Korean adults based on the timing of almond consumption. Participants were randomly assigned to one of three groups: (1) a pre-meal group (PM; n = 58) in which participants were instructed to consume 56 g of almonds per day as a preload when having regular meals; (2) a snack group (SN; n =55) in which participants were instructed to consume 56 g of almonds between meals as snacks; and (3) a control group (CL; n = 56) in which participants were provided high-carbohydrate iso-caloric control food. The three-day diet records, including two consecutive weekdays and one weekend day, were done once before the trial and twice during the trial. Body composition was assessed through multi-frequency whole-body bioimpedance measurement using InBody 620 (Biospace Co., Ltd, Seoul, Korea).After a 12-hour fast, blood samples were taken at the baseline time point (week 0) and at weeks 8 and 16 by standard venipuncture. The serum total cholesterol and triglycerides levels were measured by the enzymatic-colorimetric method using a Cobas 8000 c702 chemistry analyzer (Roche Diagnostics; Mannheim, Germany). HDL cholesterol and LDL cholesterol levels were determined via homogeneous enzymatic colorimetry.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
20 Years to 39 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • non-smokers
  • age 20-39 yr
  • Male and Female non-smokers
  • BMI 17-30 kg/m2
  • under Korean habitual diet
  • Exclusion criteria:
  • any diseases
  • any weight change 6 mo before the study
  • \>2 times/wk nut consumption
  • frequent alcohol consumption

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Changes of body fat percentages from baseline

Time Frame: week 20

Changes of blood lipid profiles from baseline

Time Frame: week 20

Secondary Outcomes

  • Changes of blood IL-6 levels(week 16)

Investigators

Sponsor
ICAN Nutrition Education and Research
Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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