Actively Recruiting

Phase Not Applicable
Age: 24Years - 70Years
All Genders
NCT06695221

Improving Health Outcomes With Kefir

Led by University of Alberta · Updated on 2026-05-08

156

Participants Needed

1

Research Sites

88 weeks

Total Duration

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AI-Summary

What this Trial Is About

The purpose of the study is to ascertain whether traditional kefir not only enhances vascular health but also contributes to improved immune outcomes in both male and female participants at higher risk or living with Type 2 Diabetes (T2D) after 12 weeks of treatment.

CONDITIONS

Official Title

Improving Health Outcomes With Kefir

Who Can Participate

Age: 24Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Females and males aged 24 to 70 years living in Edmonton or nearby areas within driving distance
  • Overweight or obesity (BMI >25 for Caucasians, >23 for Asians)
  • At higher risk of Type 2 Diabetes (fasting blood glucose 5.6-6.9 mmol/L or HbA1c 5.5-6.4%)
  • Diagnosed with Type 2 Diabetes (fasting blood glucose ≥7.0 mmol/L or HbA1c ≥6.5%)
Not Eligible

You will not qualify if you...

  • Regular high intake of fermented foods (more than 3 servings per week) other than cheese in the past 3 months
  • Any gastrointestinal disorders
  • Pregnant or breastfeeding
  • Monogenic dyslipidemias and endocrine disorders other than diabetes
  • Use of medications such as antibiotics, antifungals, corticosteroids, methotrexate, or immunosuppressive cytotoxic agents in the last 3 months
  • Health conditions that could interfere with study outcomes (e.g., kidney disease, liver disease, cancer, gastrointestinal surgery, heavy alcohol use)
  • Having a pacemaker or any electrical medical device that prevents undergoing bioelectrical impedance analysis (BIA) test

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Alberta

Edmonton, Alberta, Canada, T6G 2E1

Actively Recruiting

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Research Team

P

Paulina Aldana Hernandez, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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