RecruitingNot ApplicableNCT06695221
Improving Health Outcomes With Kefir
Sponsor
University of Alberta
Enrollment
156 participants
Start Date
Mar 24, 2026
Study Type
INTERVENTIONAL
Conditions
Summary
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.
Eligibility
Min Age: 24 YearsMax Age: 70 Years
Inclusion Criteria4
- females and males (24-70 years old) living in Edmonton (or Edmonton area/driving distance);
- overweight or obesity (BMI \>25 Caucasian, \>23 Asian);
- at higher risk of T2D (fasting blood glucose ≥ 5.6 - 6.9 mmol/L or/and HbA1C ≥ 5.5 - 6.4%); or
- with diagnosis of T2D (fasting blood glucose ≥ 7.0 mmol/L or/and HbA1C ≥ 6.5%).
Exclusion Criteria7
- a usual high intake (maximum intake 3 servings/week) of fermented foods excluding cheese (i.e., kefir, kombucha, kimchi, etc.) for the past 3 months;
- gastrointestinal (GI) disorders of any kind;
- being pregnant or breastfeeding;
- monogenic dyslipidemias and endocrine disorders except for diabetes;
- use of medications within the last 3 months (i.e., antibiotics or antifungals, corticosteroids, methotrexate, or immunosuppressive cytotoxic agents);
- any health conditions deemed to interfere with primary outcomes at the investigator's discretion (e.g., kidney disease, liver disease, cancer, GI surgery, heavy alcohol consumption, etc.);
- having a pacemaker or any electrical medical device that prevents the individual from undergoing the bioelectrical impedance analysis bioimmunoassay (BIA) test."
Interventions
DIETARY_SUPPLEMENTTraditional Kefir
350 mL/day of traditional fermented/prepared kefir
DIETARY_SUPPLEMENTMilk (placebo)
350 mL/day of commercial 2% fat milk
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06695221
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