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RecruitingNCT06695221

Improving Health Outcomes With Kefir

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
156 (estimated)
Sponsor
University of Alberta · Academic / Other
Sex
All
Age
24 Years – 70 Years
Healthy volunteers
Not accepted

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.

Detailed description

Participants who sign the written consent form will undergo a screening process to determine eligibility for study entry. At the baseline visit, recruited participants will be randomized in a double-blind manner (participant and study coordinator) to consume either 350 mL of traditional fermented kefir or 350 mL of a placebo (milk) daily. During the 12 weeks of intervention, health outcomes will be measured and collected for further analysis.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTTraditional Kefir350 mL/day of traditional fermented/prepared kefir
DIETARY_SUPPLEMENTMilk (placebo)350 mL/day of commercial 2% fat milk

Timeline

Start date
2026-03-24
Primary completion
2027-12-01
Completion
2027-12-01
First posted
2024-11-19
Last updated
2026-03-12

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT06695221. Inclusion in this directory is not an endorsement.

Improving Health Outcomes With Kefir (NCT06695221) · Clinical Trials Directory