Actively Recruiting
Effects of Akkermansia Muciniphila and Berberine Supplementation on Insulin Sensitivity in Night-shift Workers
Led by FH Joanneum Gesellschaft mbH · Updated on 2026-02-27
200
Participants Needed
1
Research Sites
106 weeks
Total Duration
On this page
Sponsors
F
FH Joanneum Gesellschaft mbH
Lead Sponsor
M
Medical University of Vienna
Collaborating Sponsor
AI-Summary
What this Trial Is About
Night shift work is associated with an increased risk of obesity, insulin resistance, and cardiometabolic disorders, largely due to circadian misalignment, disrupted sleep, and altered eating patterns. These behavioral and physiological disturbances impair glucose metabolism and are further influenced by the gut microbiota. In particular, the bacterium Akkermansia muciniphila has been linked to improved metabolic health, including enhanced insulin sensitivity, lipid regulation, and maintenance of intestinal barrier integrity. Berberine, a bioactive plant-derived compound, has demonstrated metabolic benefits, including upregulation of A. muciniphila, improvement of insulin sensitivity, and modulation of lipid metabolism. Together, these complementary mechanisms suggest that combined A. muciniphila supplementation and berberine administration may synergistically improve metabolic health in shift workers by targeting gut microbiota composition and circadian-regulated metabolic pathways. Based on this rationale, a double-blind, randomized, placebo-controlled, crossover study is being conducted in 200 night-shift workers from healthcare and industrial sectors in Austria and Denmark. Participants are stratified by age, sex, and work sector and randomly assigned to intervention sequences. Each participant receives either the combined supplement or placebo for 12 weeks, followed by a four-week washout, after which the alternate intervention is administered for another 12 weeks, with a total participation of 28 weeks. Assessments are performed at four study visits and include anthropometry, body composition, blood pressure, and collection of blood, urine, and feces. Participants complete validated questionnaires on dietary intake, lifestyle, work schedules, and general health to monitor behavioral patterns throughout the study. Dietary intake is recorded for four days prior to each sampling visit in consideration of shift schedules. Sleep duration and quality are monitored via diaries and actigraphy and aligned with dietary records. Circadian variation is minimized by standardizing sampling times and implementing a fasting and synchronization period prior to visits. The primary outcome is insulin sensitivity, measured by HOMA-IR. Secondary exploratory outcomes include gut microbiota composition and diversity, biomarkers of intestinal permeability and inflammation, lipid profiles, body composition, sleep quality, and dietary behavior. These measures collectively provide a comprehensive evaluation of the metabolic, microbiome, and circadian effects of combined A. muciniphila and berberine supplementation in night-shift workers.
CONDITIONS
Official Title
Effects of Akkermansia Muciniphila and Berberine Supplementation on Insulin Sensitivity in Night-shift Workers
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Health care or industrial shift worker
- Employed or self-employed working at least 24 hours per week
- Currently working night shifts that include at least 3 hours between midnight and 5 a.m.
- Night shift work duration longer than 3 years
- At least 4 night shifts per month
You will not qualify if you...
- Body mass index (BMI) of 40 kg/m² or higher
- Pregnant, planning pregnancy within 6 months, or breastfeeding
- History of bariatric surgery
- Surgery within 3 months before the study or planned surgery in the next 6 months that may affect study outcomes
- Diagnosed type 1 or type 2 diabetes
- Uncontrolled thyroid disease without stable medication for more than 3 months
- Chronic diseases such as renal failure, active hepatitis, liver cirrhosis, recent myocardial infarction, stroke, COPD, or cancer
- Immunodeficiency, active autoimmune or autoinflammatory diseases, inflammatory bowel disease, or acute atopic disease episodes
- Regular use of anticoagulants
- Known allergy to any ingredients in the study products
- Participation in other clinical trials during this study
- Current or planned weight loss programs, extreme diets, or vigorous exercise routines that quickly raise heart rate
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
FH JOANNEUM University of Applied Sciences
Graz, Styria, Austria, 8020
Actively Recruiting
Research Team
M
Miriam Ressler, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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