Lifestyle-related ConditionLEGUMINIBUSNCT05999136
Effects of Pulses Through the Gut Microbiome and Bioavailability of Bioactive Compounds
A study testing Pulses diet, Plant proteins diet and Habitual diet in people with Lifestyle-related Condition, run by Paola Vitaglione at 1 site in Italy.
Trial summary
The goal of this clinical trial is to investigate the effects of replacing red meat with pulses, on cardiometabolic health and gut microbiome in individuals with unhealthy habits and sedentary lifestyles at high risk for cardiovascular diseases. The main questions it aims to answer are: 1. Read more about this study
- Who is it for?
- Ages 18 to 65 yearsHealthy volunteers can take part
- Conditions the study is for
- Lifestyle-related Condition
- What is being tested?
- Pulses diet, Plant proteins diet and Habitual diet
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 84 participants
- Where
- 1 siteItaly
- Study dates
- 10 Jan 2024to 20 Dec 2024
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- men and women aged 18-65;
- 20 ≤ BMI ≤ 35 kg/m2;
- habitual diet characterized by ≥ 3 medium servings of fresh red meat or processed meat (equivalent to a portion weight of 100g of fresh meat and 50g of cured meats);
- habitual diet without probiotics, functional foods, and/or any type of food supplements;
- low level of physical activity (sedentary lifestyle);
- signing the informed consent form and expressing consent for the processing of personal data.
Who cannot join
- Food allergies and intolerances, such as celiac disease, lactose intolerance, and others;
- Gastrointestinal disorders of any kind;
- Significant medical conditions;
- Pregnancy or breastfeeding;
- Hypertriglyceridemia (Triglycerides > 200 mg/dL);
- Hypercholesterolemia (Cholesterol > 200 mg/dL);
Show all 13Show fewer
- Diabetes (Blood glucose ≥ 126 mg/dL);
- Hypertension (Blood pressure > 140/90 mm Hg);
- Weight loss ≥ 3 kg in the past 2 months prior to the study;
- Use of any medication at enrollment and in the 2 months prior to the study;
- Regular diet rich in fruits and vegetables;
- Consumption of alcohol equivalent to or exceeding 3 glasses of wine per day;
- Concurrent participation in other clinical trials.
Trial locations and contacts
1 site in 1 country.
Italy1 site
Department of Agricultural Sciences, Federico II University
Portici, 80055
About this study
Official title: Discovering the Effects of Pulses Through the Gut Microbiome and Bioavailability of Bioactive Compounds
The goal of this clinical trial is to investigate the effects of replacing red meat with pulses, on cardiometabolic health and gut microbiome in individuals with unhealthy habits and sedentary lifestyles at high risk for cardiovascular diseases. The main questions it aims to answer are:
- How does the substitution of red meat with pulses affect some markers of cardiovascular risk?
- How does this dietary intervention influence the composition and function of the gut microbiome, nutritional status, well-being indices, and biomarkers related to metabolic, oxidative, inflammatory, immune, and intestinal permeability status?
Read more
Participants will:
- be assigned to either the Pulses Diet (PulD) group or the Plant Proteins Diet (PPD) group or the Habitual diet (HabD) group;
- follow their habitual diet (HabD) or the prescribed dietary plan designed on individual habitual diet to be isocaloric and isoprotein but replacing red meat with pulses (PulD group) or a combination of pulses and plant-based meat substitutes (PPD group);
- keep their physical activity levels unchanged during the entire intervention period;
- be required to complete 7-day food diaries and associated questionnaires on appetite, along with additional questionnaires related to physical activity levels, overall well-being, mood, sleep quality, stool frequency and consistency at each nutritional intervention time-point.
Researchers will compare PulD, PPD, and HabD to assess if the dietary interventions have an impact on cardiometabolic health and gut microbiome.
Read the detailed description
Legumes are recognized for their distinctive nutritional profile, rich in plant-based proteins, low-glycemic-index carbohydrates, fiber, B vitamins, minerals, and polyphenols. Due to their protein content and amino acid composition, legumes in combination with grains can effectively replace meat and its derivatives. Despite worldwide nutritional guidelines recommending legumes as the predominant source of dietary protein, the consumption of red meat and meat products remains high and may have negative consequences for public health. Indeed, epidemiological evidence indicates that long-term consumption of increasing amounts of red and processed meats is associated with a higher risk of mortality, cardiovascular diseases, colon cancer, and type 2 diabetes. Furthermore, a recent study has shown that higher intake of red meat and choline is associated with higher concentrations of trimethylamine-N-oxide (TMAO), a gut microbiota byproduct that has been associated with a higher incidence of adverse cardiovascular events. Numerous research studies indicate that the consumption of plant-based foods brings health benefits for humans and supports the recommendation of international guidelines to modify dietary habits towards a diet richer in plant-based products. In addition, epidemiological studies show a possible association between high legume consumption and a decrease in coronary heart disease and colorectal adenoma, while the evidence for a protective role of legumes against cardiovascular diseases is less strong due to heterogeneity in results and/or potential confounding factors. The ability of legumes to reduce cardiometabolic risk factors is also supported by various scientific evidence from clinical trials. These studies demonstrate that legume consumption has a positive effect on lipid profile, glucose metabolism, blood pressure, body weight, oxidative stress, and inflammatory status.
Despite the recognized health benefits of consuming legumes regularly, there is still a limited understanding of the underlying physiological mechanisms that drive these positive effects. An observational study conducted in Italy shed some light on this issue by demonstrating that individuals who closely adhere to the Mediterranean diet, which emphasizes reducing red meat consumption and increasing the intake of fruits, vegetables, and legumes, have gut microbiota characterized by a higher abundance of fiber-degrading bacteria. These individuals also exhibit higher levels of short-chain fatty acids in their feces and lower concentrations of TMAO in their urine. Furthermore, a randomized controlled trial conducted on individuals at risk of cardiovascular diseases due to an unhealthy lifestyle revealed that shifting from a typical Western diet to a more Mediterranean-like pattern led to an increase in the presence of fiber-degrading bacterial species in the gut microbiota. This dietary change also resulted in elevated circulating microbial metabolites associated with improved inflammatory status. While there is still a lack of comprehensive in vivo studies assessing the bioavailability of nutrients from legumes, a few clinical trials have investigated the influence of legumes on the intestinal microbiome. Nevertheless, the available literature indicates that legumes have the ability to influence the human microbiota. However, it is important to note that the specific effects of legumes on the microbiota can vary significantly across different studies, making it difficult to generalize these findings to all types of legumes.
In this framework, the present project will focus on the evaluation of the effect of replacing red meat with pulses (PulD) or a combination of pulses and plant-based meat substitutes (PPD) on the cardiometabolic health of individuals with unhealthy habits and sedentary lifestyles via the modification of intestinal microbial communities. Additionally, it seeks to investigate the effects on health outcomes, with a primary focus on evaluating changes in inflammatory, oxidative, immune, and hormonal status. The study will include the establishment of a 2-month dietary intervention with an isocaloric and isoprotein pulses diet (PulD) and a plant proteins diet (PPD). Coupled with detailed host phenotyping and gut microbiota profiling during and after the intervention, this will allow assessment of the causal effects of a diet rich in plant-based proteins (mainly from pulses) and the gut microbiome in populations at high risk for cardiovascular disease (CVD).
The potential eligibility of subjects to participate in this study will be assessed through pre-recruitment questionnaires. These questionnaires will collect personal and socio-demographic data of volunteers, general health information (including anthropometry, health status, medical history, smoking and alcohol consumption habits), details about individual dietary habits using the Food Frequency Questionnaire (FFQ), information about eating behavior through the Three Factor Eating Questionnaire (TFEQ), and levels of physical activity using the International Physical Activity Questionnaire (IPAQ). Subjects in the PulD group and PPD group will be assigned a personalized diet prepared on the basis of own eating habits as established by 7-day food diary recalls. Energy values and whole macronutrient composition of habitual diets will be kept unchanged during PulD and PPD intervention. However, changes in carbohydrate (dietary fibre vs. starch), dietary fat (saturated vs. mono/polyunsaturated fatty acids), and protein (vegetable vs. animal) composition will be applied as a consequence of replacing meat with pulses (PulD group) or with a mix of pulses and plant-based meat substitutes (PPD group). Control subjects will not change their habitual diet (HabD) during intervention. All subjects will be requested not to change physical activity levels during the 8 weeks intervention period. Compliance will be assessed every 2 weeks with a phone interview in order to evaluate the dietary intake and physical activity during the previous week. At each intervention time-point (baseline, 4 weeks, 8 weeks), for the nutritional check, subjects will complete 7-day food diaries and associated questionnaires on appetite (Visual Analog Scale, VAS) related to the previous week before the nutritional analysis. Additionally, measurements of blood pressure, weight, circumferences (waist and hips), and body composition through bioimpedance testing will be conducted. During the intervention period, subjects will be asked to fill out the International Physical Activity Questionnaire (IPAQ), questionnaires on quality of life (QoL), on depression, anxiety and stress (DASS), the King's Stool Chart (KSC) to evaluate frequency, weight, and consistency of feces, along with the Pittsburgh Sleep Quality Index (PSQI) to evaluate the quality of sleep.
Further analysis of compliance will be conducted based on metabolomics, allowing discrimination of animal/vegetable protein intake. Metabolomes (well known to reflect both diet and microbial metabolism) will also be compared between categories in order to identify protective or risk profiles using both bioinformatics and chemometrics approaches. Metagenomes will be analyzed following Standard Operating Procedures (SOPs) utilized in landmark studies already published. Comparison of predefined groups of individuals will allow identification of microbial genes that have different abundance in the groups. Furthermore, genes will be associated with continuous variables of clinical and nutritional interest (e.g., intake of specific dietary components, insulin sensitivity) by covariance analysis. Concatenated datasets of physiological output data, metagenomic and metabolome profiles from the intervention studies will be used to predict subsets of features by multivariate analysis (PLS-DA) that can classify subjects according to their relative adherence to a PulD or PPD. The profile will be used to probe the microbiome for specific alterations as a function of the interventions.
The sample size needed to detect an effect of PulD and/or PPD on individual TMAO levels is defined based on previous study from Crimarco and colleagues. It was calculated that a sample of 28 participants per group would allow detecting a minimum difference of approximately -1.3 μM (-38%) in TMAO and approximately -0.9 mM (-18%) in cholesterol between each of the 2 test treatments vs. control and between the two test treatments, with a power of 80% and an α-error 0.017 to account for multiple comparisons (T-test).
- Conditions
- Lifestyle-related Condition
- Being tested
- Pulses diet, Plant proteins diet, Habitual diet
- Keywords
- Gut microbiome, Legumes, Pulses, Plant proteins, Cardiovascular diseases, Red meat substitution, Protein transition, Overweight, Obesity
- Medical subject headings
- Mental Disorders, Cardiovascular Diseases, Overweight, Obesity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Pulses dietOther
Subjects in the PulD group will be assigned a personalized diet prepared based on their own eating habits as established by 7-day food diary recalls. Energy values of habitual diets will be kept unchanged during the PulD intervention. The diet will be characterized by isocaloric and isoprotein substitutions, replacing habitual servings of red meat or processed meat with servings of pulses.
Plant proteins dietOther
Subjects in the PPD group will be assigned a personalized diet prepared based on their own eating habits as established by 7-day food diary recalls. Energy values of habitual diets will be kept unchanged during the PPD intervention. The diet will be characterized by isocaloric and isoprotein substitutions, replacing habitual servings of red meat or processed meat with a mixture of pulses and plant-based meat substitutes.
Habitual dietOther
Control subjects will not change their habitual diet during intervention. All subjects will be requested not to change physical activity levels during the 8 week intervention period.
| Study group | Role | What they receive |
|---|---|---|
| Pulses Diet (PulD) | Experimental | Subjects will follow a Pulses-enriched diet for 2 months. Receives: Other: Pulses diet |
| Plant Proteins Diet (PPD) | Experimental | Subjects will follow a Plant protein-enriched diet for 2 months. Receives: Other: Plant proteins diet |
| Habitual Diet (HabD) | Active comparator | Subjects will follow a habitual diet for two months. Receives: Other: Habitual diet |
What is being measured
The primary outcome is the main question the study is designed to answer.
Changes in fasting total cholesterol concentration
Measure of serum total cholesterol concentration (mg/dL serum)
Measured: 2 months
Changes in plasma TMAO concentration
Measure of plasma TMAO concentration (μmol/L plasma)
Measured: 2 months
Secondary outcomes (43)
Changes in faecal microbiome
Measure of faecal microbiome
Measured: 2 months
Changes in urinary TMAO concentration
Measure of urinary TMAO concentration (mmol/mol creatinine)
Measured: 2 months
Changes in urinary polyphenols concentration
Measure of urinary polyphenols concentration (ng/mg creatinine)
Measured: 2 months
Changes in urinary urolithin concentration
Measure of urinary urolithin concentration (ng/mg creatinine)
Measured: 2 months
Changes in urinary betaine concentration
Measure of urinary betaine concentration (mmol/mol creatinine)
Measured: 2 months
Changes in urinary carnitine concentration
Measure of urinary carnitine concentration (mmol/mol creatinine)
Measured: 2 months
Changes in urinary choline concentration
Measure of urinary choline concentration (mmol/mol creatinine)
Measured: 2 months
Changes in urinary tryptophan betaine concentration
Measure of urinary tryptophan betaine concentration (mmol/mol creatinine)
Measured: 2 months
Changes in urinary indican concentration
Measure of urinary indican concentration (mg/g creatinine)
Measured: 2 months
Changes in urinary creatinine concentration
Measure of urinary concentration (mg/dL)
Measured: 2 months
Variation of complete blood count
Measure of Red blood cell (RBC) count (number of cells/mm3); Hemoglobin (Hb) concentration (g/dL); Hematocrit (HCT) percentage (%); White blood cell (WBC) count (number of cells/mm3); Platelet (PLT) count (number of cells/mm3).
Measured: 2 months
Variation of blood iron status biomarkers
Measure of blood concentrations (mg/dL) of iron, ferritin, total transferrin
Measured: 2 months
Variation of vitamin B status
Measure of blood folic acid and vitamin B12 concentrations (ng/mL)
Measured: 2 months
Variation of individual hormonal status
Measure of plasma glucagon-like peptide 1 (GLP-1), Glucose-dependent Insulinotropic Peptide (GIP), Glucagon, Leptin, Ghrelin, C-peptide concentrations (pg/mL plasma)
Measured: 2 months
Variation of plasma endocannabinoids concentration
Measure of plasma endocannabinoids concentration (ng/mL)
Measured: 2 months
Variation of plasma N-acylethanolamines concentration
Measure of plasma N-acylethanolamines concentration (ng/mL)
Measured: 2 months
Changes in plasma betaine concentration
Measure of plasma betaine concentration (μmol/L plasma)
Measured: 2 months
Changes in plasma carnitine concentration
Measure of plasma carnitine concentration (μmol/L plasma)
Measured: 2 months
Changes in plasma choline concentration
Measure of plasma choline concentration (μmol/L plasma)
Measured: 2 months
Changes in plasma bioactive peptides concentration
Measure of plasma bioactive peptides concentration (ng/mL plasma)
Measured: 2 months
Changes in plasma bile acids concentration
Measure of plasma bile acids concentration (ng/mL plasma)
Measured: 2 months
Variation of plasma oxidative stress biomarkers
Measure in plasma of: TBARS concentration (µM); nitrotyrosine (N-Tyr) concentration (OD/mL); 8-hydroxy-2-deoxyguanosine (8-OHdG) concentration (ng/mL)
Measured: 2 months
Variation of plasma antioxidant enzyme activities
Measure of plasma superoxide dismutase (SOD) activity (U/mL); catalase activity (nmol/min/mL); glutathione peroxidase (GPx) activity (nmol/min/mL)
Measured: 2 months
Variation of serum dipeptidyl peptidase-IV (DPP-IV) concentration and activity
Measure of serum dipeptidyl peptidase-IV (DPP-IV) concentration (ng/mL) and activity (IU/L)
Measured: 2 months
Variation of serum Triglycerides concentration
Measure of serum triglycerides concentration (mg/dL serum)
Measured: 2 months
Variation of serum LDL- and HDL-cholesterol concentrations
Measure of serum LDL-, HDL-cholesterol concentrations (mg/dL serum)
Measured: 2 months
Variation of serum glucose concentration
Measure of serum glucose concentration (mg/dL)
Measured: 2 months
Variation of serum insulin concentration
Measure of serum insulin concentration (μU/mL serum)
Measured: 2 months
Variation of serum Insulin-like Growth Factor-1 (IGF-1) concentration
Measure of serum IGF-1 concentration (ng/mL)
Measured: 2 months
Variation of serum C-reactive protein (CRP) concentration
Measure of serum CRP concentration (mg/L)
Measured: 2 months
Variation of serum zonulin concentration
Measure of serum zonulin concentration (ng/mL)
Measured: 2 months
Changes in immune state blood markers
Measure of monocyte polarization (Arbitrary Units) of Cluster of Differentiation (CD) 86, Tumor Necrosis Factor alpha (TNFα), inducible Nitric Oxide Synthase (iNOS), CD36, CD11c, CD169, CD206, CD163, CD68, CD11b, CD16, e CD14
Measured: 2 months
Variation of erythrocytes antioxidant enzymes activity
Measure in erythrocytes of: superoxide dismutase (SOD) activity (U/mL); catalase activity (nmol/min/mL); glutathione peroxidase (GPx) activity (nmol/min/mL); glutathione reductase (GR) activity (U/mL)
Measured: 2 months
Changes in body weight
Measure of body weight (kg) in fasting subjects
Measured: 2 months
Changes in body mass index
Calculation of body mass index (kg/m2) by using the formula weight in kilograms divided by height in meters squared.
Measured: 2 months
Changes in waist and hip circumferences
Measure of waist circumference (cm) at the midpoint between the lower margin of the least palpable rib and the top of the iliac crest.
Measure of hip circumference (cm) around the widest portion of the buttocks.
Measured: 2 months
Changes in blood pressure
Measure of systolic pressure and diastolic pressure in millimetres of mercury (mmHg) by using a digital sphygmomanometer
Measured: 2 months
Changes in body composition
Body composition (kg body fat mass, body fat-free mass and total body water) is determined by conventional bioelectrical impedance analysis with a single-frequency 50 kilohertz (kHz) bioelectrical impedance analyzer in the postabsorptive state (fasting subjects) and after being in the supine position for 20 min. Body composition data will be calculated from bioelectrical measurements and anthropometric data by using validated predictive equations.
Measured: 2 months
Variation of hunger, fullness and satiety sensation scores
Measures of hunger, fullness and satiety sensations over the day reported by subjects by using hunger Visual Analogue Scales (VAS) 0-10 centimeters. Changes in these scores may reflect potential effects of dietary intervention in modulating hunger, fullness and satiety.
Measured: 2 months
Changes in stool weight, consistency and frequency
Measure of stool weight, frequency and consistency by mean of King's Stool Chart (KSC) filled out by subjects. The chart comprises three categories of stool weight : <100 g, 100-200 g, >200 g. The chart comprises four categories of stool consistency: hard and formed, soft and formed, loose and unformed, liquid. Fecal frequency is incorporated by recording the code of each feces passed over a 24 hour period.
Measured: 2 months
Assessment of diet composition
Measure of individual's usual food consumption through Food Frequency Questionnaires (FFQ) by querying the frequency (times/week) and amount (g) at which the respondent consumed food items based on a predefined food list.
Measured: 2 months
Changes in physical activity level
Measurement of an individual's physical activity level (MET min/week) through the International Physical Activity Questionnaire (IPAQ), which assesses the frequency (times/week) and duration (min) of different activities such as walking, moderate-intensity exercises, vigorous-intensity exercises, and sitting time.
Measured: 2 months
Variation of wellbeing status
Estimate of wellbeing status by mean of quality of life (QoL) questionnaire, which is based on Short Form-12 Health Survey (SF-12), a self-report form of subjective health. Physical and Mental Health Composite Scores (PCS \& MCS, arbitrary units) are computed using the scores of twelve questions and range from 0 to 100, where a zero score indicates the lowest level of health measured by the scales and 100 indicates the highest level of health.
Measured: 2 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Aug 2023
- Study start10 Jan 2024
- Primary completion20 Dec 2024
- Study completion20 Dec 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Lifestyle-related ConditionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 84 participants (actual)
Sponsor and investigators
- Lead sponsor
- Paola Vitaglione
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Paola Vitaglione, Federico II University
- Investigators
- Paola Vitaglione, Professor, Study director, Department of Agricultural Sciences, Federico II University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05999136
- Sponsor's protocol ID
- DE LEGUMINIBUS
- Acronym
- LEGUMINIBUS
- Status last verified
- Jun 2026
- First submitted
- 13 Aug 2023
- Last updated
- 22 Jun 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: All individual participant data that underlie the results reported in the publication will be shared after deidentification
Publications
Crimarco A, Springfield S, Petlura C, Streaty T, Cunanan K, Lee J, Fielding-Singh P, Carter MM, Topf MA, Wastyk HC, Sonnenburg ED, Sonnenburg JL, Gardner CD. A randomized crossover trial on the effect of plant-based compared with animal-based meat on trimethylamine-N-oxide and cardiovascular disease risk factors in generally healthy adults: Study With Appetizing Plantfood-Meat Eating Alternative Trial (SWAP-MEAT). Am J Clin Nutr. 2020 Nov 11;112(5):1188-1199. doi: 10.1093/ajcn/nqaa203.
PubMed 32780794Meslier V, Laiola M, Roager HM, De Filippis F, Roume H, Quinquis B, Giacco R, Mennella I, Ferracane R, Pons N, Pasolli E, Rivellese A, Dragsted LO, Vitaglione P, Ehrlich SD, Ercolini D. Mediterranean diet intervention in overweight and obese subjects lowers plasma cholesterol and causes changes in the gut microbiome and metabolome independently of energy intake. Gut. 2020 Jul;69(7):1258-1268. doi: 10.1136/gutjnl-2019-320438. Epub 2020 Feb 19.
PubMed 32075887
Study at a glance
From the registry record, last updated by the sponsor on 22 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Discovering the Effects of Pulses Through the Gut Microbiome and Bioavailability of Bioactive Compounds
- ClinicalTrials.gov ID
- NCT05999136
- Acronym / sponsor ID
- LEGUMINIBUS / DE LEGUMINIBUS
- Conditions
- Lifestyle-related Condition
- Keywords
- Gut microbiome, Legumes, Pulses, Plant proteins, Cardiovascular diseases, Red meat substitution, Protein transition, Overweight
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 84 participants (actual)
- Lead sponsor
- Paola VitaglioneUniversity, hospital or other
- Study start
- 10 Jan 2024 (actual)
- Primary completion
- 20 Dec 2024 (actual)
- Study completion
- 20 Dec 2024 (actual)
- First posted
- 21 Aug 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this clinical trial is to investigate the effects of replacing red meat with pulses, on cardiometabolic health and gut microbiome in individuals with unhealthy habits and sedentary lifestyles at high risk for cardiovascular diseases. The main questions it aims to answer are:
- How does the substitution of red meat with pulses affect some markers of cardiovascular risk?
- How does this dietary intervention influence the composition and function of the gut microbiome, nutritional status, well-being indices, and biomarkers related to metabolic, oxidative, inflammatory, immune, and intestinal permeability status?
Participants will:
- be assigned to either the Pulses Diet (PulD) group or the Plant Proteins Diet (PPD) group or the Habitual diet (HabD) group;
- follow their habitual diet (HabD) or the prescribed dietary plan designed on individual habitual diet to be isocaloric and isoprotein but replacing red meat with pulses (PulD group) or a combination of pulses and plant-based meat substitutes (PPD group);
- keep their physical activity levels unchanged during the entire intervention period;
- be required to complete 7-day food diaries and associated questionnaires on appetite, along with additional questionnaires related to physical activity levels, overall well-being, mood, sleep quality, stool frequency and consistency at each nutritional intervention time-point.
Researchers will compare PulD, PPD, and HabD to assess if the dietary interventions have an impact on cardiometabolic health and gut microbiome.
Detailed description
Legumes are recognized for their distinctive nutritional profile, rich in plant-based proteins, low-glycemic-index carbohydrates, fiber, B vitamins, minerals, and polyphenols. Due to their protein content and amino acid composition, legumes in combination with grains can effectively replace meat and its derivatives. Despite worldwide nutritional guidelines recommending legumes as the predominant source of dietary protein, the consumption of red meat and meat products remains high and may have negative consequences for public health. Indeed, epidemiological evidence indicates that long-term consumption of increasing amounts of red and processed meats is associated with a higher risk of mortality, cardiovascular diseases, colon cancer, and type 2 diabetes. Furthermore, a recent study has shown that higher intake of red meat and choline is associated with higher concentrations of trimethylamine-N-oxide (TMAO), a gut microbiota byproduct that has been associated with a higher incidence of adverse cardiovascular events. Numerous research studies indicate that the consumption of plant-based foods brings health benefits for humans and supports the recommendation of international guidelines to modify dietary habits towards a diet richer in plant-based products. In addition, epidemiological studies show a possible association between high legume consumption and a decrease in coronary heart disease and colorectal adenoma, while the evidence for a protective role of legumes against cardiovascular diseases is less strong due to heterogeneity in results and/or potential confounding factors. The ability of legumes to reduce cardiometabolic risk factors is also supported by various scientific evidence from clinical trials. These studies demonstrate that legume consumption has a positive effect on lipid profile, glucose metabolism, blood pressure, body weight, oxidative stress, and inflammatory status.
Despite the recognized health benefits of consuming legumes regularly, there is still a limited understanding of the underlying physiological mechanisms that drive these positive effects. An observational study conducted in Italy shed some light on this issue by demonstrating that individuals who closely adhere to the Mediterranean diet, which emphasizes reducing red meat consumption and increasing the intake of fruits, vegetables, and legumes, have gut microbiota characterized by a higher abundance of fiber-degrading bacteria. These individuals also exhibit higher levels of short-chain fatty acids in their feces and lower concentrations of TMAO in their urine. Furthermore, a randomized controlled trial conducted on individuals at risk of cardiovascular diseases due to an unhealthy lifestyle revealed that shifting from a typical Western diet to a more Mediterranean-like pattern led to an increase in the presence of fiber-degrading bacterial species in the gut microbiota. This dietary change also resulted in elevated circulating microbial metabolites associated with improved inflammatory status. While there is still a lack of comprehensive in vivo studies assessing the bioavailability of nutrients from legumes, a few clinical trials have investigated the influence of legumes on the intestinal microbiome. Nevertheless, the available literature indicates that legumes have the ability to influence the human microbiota. However, it is important to note that the specific effects of legumes on the microbiota can vary significantly across different studies, making it difficult to generalize these findings to all types of legumes.
In this framework, the present project will focus on the evaluation of the effect of replacing red meat with pulses (PulD) or a combination of pulses and plant-based meat substitutes (PPD) on the cardiometabolic health of individuals with unhealthy habits and sedentary lifestyles via the modification of intestinal microbial communities. Additionally, it seeks to investigate the effects on health outcomes, with a primary focus on evaluating changes in inflammatory, oxidative, immune, and hormonal status. The study will include the establishment of a 2-month dietary intervention with an isocaloric and isoprotein pulses diet (PulD) and a plant proteins diet (PPD). Coupled with detailed host phenotyping and gut microbiota profiling during and after the intervention, this will allow assessment of the causal effects of a diet rich in plant-based proteins (mainly from pulses) and the gut microbiome in populations at high risk for cardiovascular disease (CVD).
The potential eligibility of subjects to participate in this study will be assessed through pre-recruitment questionnaires. These questionnaires will collect personal and socio-demographic data of volunteers, general health information (including anthropometry, health status, medical history, smoking and alcohol consumption habits), details about individual dietary habits using the Food Frequency Questionnaire (FFQ), information about eating behavior through the Three Factor Eating Questionnaire (TFEQ), and levels of physical activity using the International Physical Activity Questionnaire (IPAQ). Subjects in the PulD group and PPD group will be assigned a personalized diet prepared on the basis of own eating habits as established by 7-day food diary recalls. Energy values and whole macronutrient composition of habitual diets will be kept unchanged during PulD and PPD intervention. However, changes in carbohydrate (dietary fibre vs. starch), dietary fat (saturated vs. mono/polyunsaturated fatty acids), and protein (vegetable vs. animal) composition will be applied as a consequence of replacing meat with pulses (PulD group) or with a mix of pulses and plant-based meat substitutes (PPD group). Control subjects will not change their habitual diet (HabD) during intervention. All subjects will be requested not to change physical activity levels during the 8 weeks intervention period. Compliance will be assessed every 2 weeks with a phone interview in order to evaluate the dietary intake and physical activity during the previous week. At each intervention time-point (baseline, 4 weeks, 8 weeks), for the nutritional check, subjects will complete 7-day food diaries and associated questionnaires on appetite (Visual Analog Scale, VAS) related to the previous week before the nutritional analysis. Additionally, measurements of blood pressure, weight, circumferences (waist and hips), and body composition through bioimpedance testing will be conducted. During the intervention period, subjects will be asked to fill out the International Physical Activity Questionnaire (IPAQ), questionnaires on quality of life (QoL), on depression, anxiety and stress (DASS), the King's Stool Chart (KSC) to evaluate frequency, weight, and consistency of feces, along with the Pittsburgh Sleep Quality Index (PSQI) to evaluate the quality of sleep.
Further analysis of compliance will be conducted based on metabolomics, allowing discrimination of animal/vegetable protein intake. Metabolomes (well known to reflect both diet and microbial metabolism) will also be compared between categories in order to identify protective or risk profiles using both bioinformatics and chemometrics approaches. Metagenomes will be analyzed following Standard Operating Procedures (SOPs) utilized in landmark studies already published. Comparison of predefined groups of individuals will allow identification of microbial genes that have different abundance in the groups. Furthermore, genes will be associated with continuous variables of clinical and nutritional interest (e.g., intake of specific dietary components, insulin sensitivity) by covariance analysis. Concatenated datasets of physiological output data, metagenomic and metabolome profiles from the intervention studies will be used to predict subsets of features by multivariate analysis (PLS-DA) that can classify subjects according to their relative adherence to a PulD or PPD. The profile will be used to probe the microbiome for specific alterations as a function of the interventions.
The sample size needed to detect an effect of PulD and/or PPD on individual TMAO levels is defined based on previous study from Crimarco and colleagues. It was calculated that a sample of 28 participants per group would allow detecting a minimum difference of approximately -1.3 μM (-38%) in TMAO and approximately -0.9 mM (-18%) in cholesterol between each of the 2 test treatments vs. control and between the two test treatments, with a power of 80% and an α-error 0.017 to account for multiple comparisons (T-test).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Pulses Diet (PulD) | Experimental | Other: Pulses dietSubjects will follow a Pulses-enriched diet for 2 months. |
| Plant Proteins Diet (PPD) | Experimental | Other: Plant proteins dietSubjects will follow a Plant protein-enriched diet for 2 months. |
| Habitual Diet (HabD) | Active comparator | Other: Habitual dietSubjects will follow a habitual diet for two months. |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- men and women aged 18-65;
- 20 ≤ BMI ≤ 35 kg/m2;
- habitual diet characterized by ≥ 3 medium servings of fresh red meat or processed meat (equivalent to a portion weight of 100g of fresh meat and 50g of cured meats);
- habitual diet without probiotics, functional foods, and/or any type of food supplements;
- low level of physical activity (sedentary lifestyle);
Key exclusion criteria (13 listed)
- Food allergies and intolerances, such as celiac disease, lactose intolerance, and others;
- Gastrointestinal disorders of any kind;
- Significant medical conditions;
- Pregnancy or breastfeeding;
- Hypertriglyceridemia (Triglycerides > 200 mg/dL);
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Pulses dietSubjects in the PulD group will be assigned a personalized diet prepared based on their own eating habits as established by 7-day food diary recalls. Energy values of habitual diets will be kept unchanged during the PulD intervention. The diet will be characterized by isocaloric and isoprotein substitutions, replacing habitual servings of red meat or processed meat with servings of pulses. | Other | Pulses Diet (PulD) |
| Plant proteins dietSubjects in the PPD group will be assigned a personalized diet prepared based on their own eating habits as established by 7-day food diary recalls. Energy values of habitual diets will be kept unchanged during the PPD intervention. The diet will be characterized by isocaloric and isoprotein substitutions, replacing habitual servings of red meat or processed meat with a mixture of pulses and plant-based meat substitutes. | Other | Plant Proteins Diet (PPD) |
| Habitual dietControl subjects will not change their habitual diet during intervention. All subjects will be requested not to change physical activity levels during the 8 week intervention period. | Other | Habitual Diet (HabD) |
Primary outcome
Changes in fasting total cholesterol concentration
Time frame: 2 months
Measure of serum total cholesterol concentration (mg/dL serum)
Changes in plasma TMAO concentration
Time frame: 2 months
Measure of plasma TMAO concentration (μmol/L plasma)
43 secondary outcomes
Changes in faecal microbiome
Time frame: 2 months
Changes in urinary TMAO concentration
Time frame: 2 months
Changes in urinary polyphenols concentration
Time frame: 2 months
Changes in urinary urolithin concentration
Time frame: 2 months
Changes in urinary betaine concentration
Time frame: 2 months
Changes in urinary carnitine concentration
Time frame: 2 months
Changes in urinary choline concentration
Time frame: 2 months
Changes in urinary tryptophan betaine concentration
Time frame: 2 months
Changes in urinary indican concentration
Time frame: 2 months
Changes in urinary creatinine concentration
Time frame: 2 months
Variation of complete blood count
Time frame: 2 months
Variation of blood iron status biomarkers
Time frame: 2 months
Variation of vitamin B status
Time frame: 2 months
Variation of individual hormonal status
Time frame: 2 months
Variation of plasma endocannabinoids concentration
Time frame: 2 months
Variation of plasma N-acylethanolamines concentration
Time frame: 2 months
Changes in plasma betaine concentration
Time frame: 2 months
Changes in plasma carnitine concentration
Time frame: 2 months
Changes in plasma choline concentration
Time frame: 2 months
Changes in plasma bioactive peptides concentration
Time frame: 2 months
Changes in plasma bile acids concentration
Time frame: 2 months
Variation of plasma oxidative stress biomarkers
Time frame: 2 months
Variation of plasma antioxidant enzyme activities
Time frame: 2 months
Variation of serum dipeptidyl peptidase-IV (DPP-IV) concentration and activity
Time frame: 2 months
Variation of serum Triglycerides concentration
Time frame: 2 months
Variation of serum LDL- and HDL-cholesterol concentrations
Time frame: 2 months
Variation of serum glucose concentration
Time frame: 2 months
Variation of serum insulin concentration
Time frame: 2 months
Variation of serum Insulin-like Growth Factor-1 (IGF-1) concentration
Time frame: 2 months
Variation of serum C-reactive protein (CRP) concentration
Time frame: 2 months
Variation of serum zonulin concentration
Time frame: 2 months
Changes in immune state blood markers
Time frame: 2 months
Variation of erythrocytes antioxidant enzymes activity
Time frame: 2 months
Changes in body weight
Time frame: 2 months
Changes in body mass index
Time frame: 2 months
Changes in waist and hip circumferences
Time frame: 2 months
Changes in blood pressure
Time frame: 2 months
Changes in body composition
Time frame: 2 months
Variation of hunger, fullness and satiety sensation scores
Time frame: 2 months
Changes in stool weight, consistency and frequency
Time frame: 2 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Jun 2026.
- Results publication: PubMed 32780794Crimarco A, Springfield S, Petlura C, Streaty T, Cunanan K, Lee J, Fielding-Singh P, Carter MM, Topf MA, Wastyk HC, Sonnenburg ED, Sonnenburg JL, Gardner CD. A randomized crossover trial on the effect of plant-based compared with animal-based meat on trimethylamine-N-oxide and cardiovascular disease risk factors in generally healthy adults: Study With Appetizing Plantfood-Meat Eating Alternative Trial (SWAP-MEAT). Am J Clin Nutr. 2020 Nov 11;112(5):1188-1199. doi: 10.1093/ajcn/nqaa203.
- Results publication: PubMed 32075887Meslier V, Laiola M, Roager HM, De Filippis F, Roume H, Quinquis B, Giacco R, Mennella I, Ferracane R, Pons N, Pasolli E, Rivellese A, Dragsted LO, Vitaglione P, Ehrlich SD, Ercolini D. Mediterranean diet intervention in overweight and obese subjects lowers plasma cholesterol and causes changes in the gut microbiome and metabolome independently of energy intake. Gut. 2020 Jul;69(7):1258-1268. doi: 10.1136/gutjnl-2019-320438. Epub 2020 Feb 19.
- Individual participant dataSharing planned: Yes. All individual participant data that underlie the results reported in the publication will be shared after deidentification
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Paola Vitaglione, Professor study director
Department of Agricultural Sciences, Federico II University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Pulses diet, Plant proteins diet and Habitual diet in people with Lifestyle-related Condition, run by Paola Vitaglione at 1 site in Italy.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 22 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Changes in fasting total cholesterol concentration (time frame: 2 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05999136, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jun 2026.