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Clinical Trials/NCT06780618
NCT06780618RecruitingNot Applicable

The Effects of Brown Rice Consumption Compared to White Rice on Postprandial Changes in Interleukin-6 and Malondialdehyde Levels in Sedentary Workers

Indonesia University1 site in 1 country30 target enrollmentStarted: January 6, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
30
Locations
1
Primary Endpoint
The Effects of Brown Rice Consumption Compared to White Rice on Postprandial Changes in Interleukin-6 and Malondialdehyde Levels in Sedentary Workers

Study Overview

Brief Summary

The goal of this clinical trial is to learn if brown rice and white rice affect oxidative stress and inflammation in office workers who don't exercise much. The main question it aims to answer is:

Does eating brown rice change MDA and IL-6 levels differently than eating white rice in people who don't exercise much?

Participants will:

Be interviewed to collect personal data, medical history, lifestyle habits, and dietary patterns.

Be measured to calculate Body Mass Index (BMI). Be interviewed to complete a questionnaire to assess their physical activity level in the past week.

Be interviewed to record all food and beverages consumed in the past 24 hours. Blood samples will be drawn twice, before and after consuming the research meal.

Be provided with a research meal consisting of rice (either brown or white), scrambled eggs, and tofu stew that must be finished within 15 to 20 minutes.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
21 Years to 59 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •healthy administrative employees,
  • •age 21-59 years,
  • •normal body mass index (18.5-22.9 kg/m2),
  • •low physical activity (≤600 METs minutes/week),
  • •assign for informed consent

Exclusion Criteria

  • •being pregnant/breastfed/menopause,
  • •consumption of herbal medicines and/or supplements within 24 hours before data collection,
  • •having history of DM, CVD, cancer, and autoimmune disease,
  • •being vegan,
  • •smoking/alcohol drinking,
  • •allergic to research food's ingredients

Arms & Interventions

white rice

Placebo Comparator

Intervention: rice wheat (placebo) (Other)

brown rice

Active Comparator

Intervention: RICE (Other)

Outcomes

Primary Outcomes

The Effects of Brown Rice Consumption Compared to White Rice on Postprandial Changes in Interleukin-6 and Malondialdehyde Levels in Sedentary Workers

Time Frame: Enrollment process to fullfil sample size at 2 weeks. The intervention will be completed in 1 day.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Wulandari Taradita

Principal Investigator

Indonesia University

Study Sites (1)

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