- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04599920
Effects of Replacing Red Meat With Legumes on Biomarkers of Chronic Diseases in Healthy Men (Leg4Life)
Effects of Replacing Red and Processed Meat With Legume-based Foods on Nutrient Intake, Nutritional Status, Food Consumption, and Biomarkers of Cardiovascular Diseases, Colorectal Cancer, and Type 2 Diabetes in Healthy Working Age Men
Study Overview
Status
Intervention / Treatment
Detailed Description
A human intervention study with healthy volunteers will be carried out to investigate the effects of partial replacement of red meat with legume-based foods on gut metabolism and markers for colorectal cancer as well as biomarkers for cardiovascular diseases and type 2 diabetes.
The study will be done in parallel-design, randomized fashion, with healthy male volunteers aged 20-65 years. Inclusion and exclusion criteria are described elsewhere. Duration of the intervention will be 6 weeks.
Intervention groups will be as follows (n=50/group):
Group 1: The habitual diet of participants is supplemented with 760 g of cooked and boneless red meat per week, representing the average meat consumption of Finnish men and supplying 25% of protein intake.
Group 2: The habitual diet of participants is supplemented with legume-based foods providing equal amount of protein as 560 g of red meat and 200 g of red meat per week.
The consumption of red meat and legumes will be kept stable throughout the intervention and participants are advised to avoid consuming any red meat or legumes in addition to those provided from the research center. The investigators also aim to investigate, whether replacing red meat with legumes induces other changes in diet. This information is be important if increasing legume consumption is recommended at the population level.
Before starting the intervention, participants will get dietary advice how to follow their diets. They will get the red meat and legume-based foods for free to help to implement the diets and to enhance compliance.
Blood, urine and fecal samples will be collected at the baseline and at the end of the intervention. Nutrient intake and food consumption during the intervention will be analyzed from 4-day food records at the baseline and at the end. Nutrient intakes will be calculated using a new Finnish 'Aromi' software.
The following data collection and analyses will be carried out at the baseline and at the end of the intervention period:
- height, weight, waist and hip circumferences
- body composition by bioelectrical impedance analysis
- resting blood pressure
- fasting lipid profile in the plasma (total cholesterol, LDL and HDL, triglycerides)
- fasting glucose and insulin, HbA1c in the blood
- high sensitive C-reactive protein
- markers for nutritional status in plasma/serum: hemoglobin, transferrin receptor, ferritin, vitamin B12, folate, vitamin D
- urea/nitrogen in the urine
- total and heme-based N-nitroso compounds in feces, concentrations of bile acids, gut microbiota
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Helsinki, Finland
- Department of Food and Nutrition, University of Helsinki
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Healthy
- Omnivorous
- No exclusion criteria listed below
Exclusion Criteria:
- Vegan
- Food allergies against ingredients in foods supplemented in the study
- Oral medication for any allergies
- Regular use of food supplements
- Extreme sports
- Inflammatory bowel disease
- Colon irritable
- Coeliac disease
- Any kind of cancer within 5 years
- Continuous antibiotics or less than 3 months of the latest antibiotics use
- Type 1 or 2 diabetes
- Hypercholesterolemia
- Hormonal, liver or kidney disease
- Alcohol consumption more than 24 measures per week
- Smoking, using snuff
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Red meat supplementation providing 25% of protein intake
A diet supplemented with 760 g of cooked and boneless red meat per week, corresponding the average consumption of red meat in Finnish men.
|
560 g of cooked and boneless red meat is replaced with legume-based foods providing the equal amount of protein.
|
|
Experimental: Red meat mostly replaced with legume-based foods
A diet supplemented with legume-based foods providing 20% of protein intake and with 200 g per week of red meat providing 5% of protein intake.
|
560 g of cooked and boneless red meat is replaced with legume-based foods providing the equal amount of protein.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in the composition of gut microbiota as a measure of modification of dietary protein composition.
Time Frame: 6 weeks
|
The composition of gut microbiota is measured using HITChip phylogenetic microarray.
|
6 weeks
|
|
Changes in the concentrations of plasma lipids as a measure of diet modification.
Time Frame: 6 weeks
|
The changes in the concentrations of total, LDL, and HDL cholesterol as well as plasma triglycerides.
|
6 weeks
|
|
Changes in the intake of nutrients and nutritional status of participants as a measure of diet modification.
Time Frame: 6 weeks
|
The changes in the markers for nutritional status in plasma/serum: hemoglobin, transferrin receptor, ferritin, vitamin B12, folate.
The intake of nutrients is calculated from 4-day food records.
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in the concentrations of N-nitroso compounds in feces.
Time Frame: 6 weeks
|
The changes in gut microbiota are analyzed as a measure of diet modification.
|
6 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Anne-Maria Pajari, PhD, University of Helsinki
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Digestive System Diseases
- Glucose Metabolism Disorders
- Metabolic Diseases
- Neoplasms
- Neoplasms by Site
- Endocrine System Diseases
- Gastrointestinal Neoplasms
- Digestive System Neoplasms
- Gastrointestinal Diseases
- Diabetes Mellitus
- Colonic Diseases
- Intestinal Diseases
- Intestinal Neoplasms
- Rectal Diseases
- Cardiovascular Diseases
- Diabetes Mellitus, Type 2
- Colorectal Neoplasms
Other Study ID Numbers
- Leg4Life-HY
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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