Actively Recruiting

Phase Not Applicable
Age: 20Years - 40Years
All Genders
Healthy Volunteers
ID04119791

A Multidisciplinary Investigation of Cardiovascular Benefits of Wild Rice

Led by University of Manitoba · Updated on 2025-03-03

48

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Cardiovascular disorders such as hypertension, heart attack, and stroke remain leading causes of illness and death globally. Unhealthy diets and inactive lifestyles are key modifiable risks for these conditions. Researchers are studying the effects of wild rice, a functional food with possible health benefits, on cardiovascular risk factors in healthy adults aged 20 to 40 over a 4-week period. This pilot study aims to explore wild rice's impact and underlying mechanisms to support future larger trials. Participants will consume one serving daily of specially prepared foods containing about 30 grams of wild rice, including fruit/vegetable salad, energy cookies, and casserole, for 28 days. These "test foods" are provided by Tall Grass Bakery. The study focuses on how regular wild rice intake may influence cardiovascular health by assessing changes in blood lipids, inflammatory markers, and gut bacteria. Throughout the study, researchers will collect blood and urine samples and perform vascular measurements at the start (day 0) and end (day 28). They will analyze serum lipids, inflammation markers, and types and amounts of fecal bacteria. The primary outcomes include changes in the gut microbiome and related macronutrient metabolism. Secondary outcomes examine improvements in blood lipid profiles and endothelial cell function. Participation lasts 4 weeks with close monitoring to assess these health indicators.

CONDITIONS

Brief Title

A Multidisciplinary Investigation of Cardiovascular Benefits of Wild Rice

Who Can Participate

Age: 20Years - 40Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Male
  • Female
  • Both genders are healthy
  • 20 - 40 years old
Not Eligible

You will not qualify if you...

  • Pregnant
  • Lactating
  • Smokers
  • Obese (Body Mass Index (BMI)  30)
  • Currently on medications for cardiovascular, diabetes, or cancer diseases

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - 28 days

Participants consume one serving of the test food containing wild rice every day over 28 days.

1 baseline visit and 1 follow-up visit

Trial Site Locations

Total: 1 location

1

St. Boniface Hospital Research Center Asper clinical

Winnipeg, Manitoba, Canada, R2H2A6

Actively Recruiting

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Research Team

M

Mohammed H Moghadasian, PhD

K

Khuong Le, Bsc

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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