Food Biodiversity and Human Health (BIOQUALIM)

February 18, 2026 updated by: Hospices Civils de Lyon

BIOQUALIM: From Cultivated Biodiversity to Prevention in Human Health

In Western countries, one of the major nutritional challenges requires reducing the proportion of animal proteins and increasing the proportion of vegetable proteins in the daily plate. Added to this nutritional challenge is an environmental challenge, with plant proteins being much less expensive to produce. However, plant proteins are mainly provided by cereals and legumes, a large diversity of which is necessary to cover the recommended daily intake of amino acids. However, given the collapse of cultivated biodiversity (loss of 75% in 100 years, FAO), the diversity of the supply is very reduced.

Furthermore, for several years, public health studies have indicated a chronic deficit in micronutrients (minerals/trace elements, vitamins, antioxidants) as well as fiber in the diet of the French population. This comes in particular from the impoverishment of the nutritional quality of the fruits/vegetables/cereals/legumes consumed. In general, diet plays a major role in the primary prevention of chronic diseases (cardiovascular, diabetes, cancer) including periodontal disease. Thus, a diet low in sugars, saturated fats and rich in fiber would reduce the appearance of periodontal disease by strengthening salivary capacity. However, certain pathogenic periodontal bacteria (such as Porphyromonas gingivalis) can migrate (blood, digestive or respiratory routes) to reach other organs and represent a risk factor for other chronic diseases. Thus, the prevention of periodontal diseases through diet control would also contribute to the prevention of other chronic diseases.

The benefit of plant-based diets to reduce the risk of cancer is now established. In addition, certain cereals such as spelled have superior nutritional qualities to common wheat, notably their protein content and they also contain higher quantities of certain bioactive compounds with anti-cancer properties (such as phytosterols).

Furthermore, the potential impact of the oral microbiota on chronic diseases is now being studied: in healthy adults, a dysbiotic periodontal microbiota may be likely to lead to systemic para-inflammation. It has also been shown that a dietary change (Mediterranean diet) could lead to a reduction in pathogenic bacteria in the oral microbiota (including P. gingivalis). However, the link between the introduction of cereals into the diet and the evolution of cancer risk factor bacteria in the oral microbiota has never been demonstrated.

This pilot clinical study plans to focus on the oral microbiota, with the aim of objectivizing a possible link between a modification of the diet by the introduction of cereals (einkorn type) and the evolution of certain bacteria of this microbiota. , notably P. gingivalis (but also T. forsythia, S. anginosus, A. actinomycetemcomitans, T. denticola and F. nucleatum), considered as cancer risk factors and thus observe an improvement in health status oral and general.

Study Overview

Study Type

Interventional

Enrollment (Actual)

31

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Lyon, France, 69000
        • Maison des professionnels

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Person between 20 and 60 years old
  • Person with an omnivorous diet
  • Person who has given free, informed, express written consent
  • Person affiliated to a French social security system
  • Person with a body mass greater than 18 kg/m²
  • Person able to attend at least 1 culinary workshop

Exclusion Criteria:

  • Person with a smoking addiction
  • Person with a known food allergy/intolerance
  • Person unable to consume dairy or solid products (e.g. chocolate milk pudding, chocolate jelly)
  • Person participating in another study related to nutrition
  • Patients at high risk of infective endocarditis
  • Person with chronic pathologies
  • Person having taken antibiotic treatment during the month preceding the start of the study
  • Pregnant, parturient or breastfeeding woman
  • Minors
  • Persons deprived of liberty by a judicial or administrative decision
  • People receiving psychiatric care
  • Persons admitted to a health or social establishment for purposes other than research
  • Adults subject to a legal protection measure (guardianship, curatorship)
  • Persons not affiliated to a social security scheme or beneficiaries of a similar scheme
  • Person with fewer than 20 natural teeth
  • Person performing interdental hygiene and/or daily mouthwashes.
  • Person wearing orthodontic appliance
  • Person with periodontal disease (stage ≥ II periodontal lesions according to the Chicago 2017 classification (i.e. PD ≥ 4 mm, and/or CAL ≥ 4 mm) and/or generalized (>30% of sites )), active caries or during dental care

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Einkorn Diet
Healthy adult volunteers (not suffering from chronic pathologies) and non-smokers, having an omnivorous diet, and agreeing to change their eating habits for 3 months (reducing meat consumption by half and replacing it with einkorn).
Analysis of the oral microbiota before (T0) and after (T2) introduction of einkorn into the diet by interdental sampling, on 4 sites, pooled then analyzed by bacterial PCR.
Other Names:
  • Total Oral microbiota
Comparison of the number of total bacteria and pathogens of the interdental microbiota before (T0) and in interim analysis (T1) for evaluation of the minimum period of effectiveness, by interdental sampling, on 4 sites, pooled then analyzed by bacterial PCR.
Analysis of the periodontal and oral clinical parameters (plaque index, gingival index, interdental inflammation, pocket depth and loss of clinical attachment, salivary pH) before (T0) and after (T2) introduction of einkorn into the diet, by sampling and periodontal analysis of all of the participants' teeth
Analysis of general health indicators (body mass index, measurement of abdominal circumference, blood pressure, MOS SF-36 quality of life questionnaire and eating habits) before (T0) and after (T2) introduction of einkorn in the diet

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Total periodontal bacteria count
Time Frame: Baseline (T0), 3 months after baseline (T2)
Comparison of the number of total bacteria and pathogens of the interdental microbiota before (T0) and after (T2) introduction of einkorn into the diet, by interdental sampling, on 4 sites, pooled then analyzed by bacterial PCR.
Baseline (T0), 3 months after baseline (T2)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Intermediate periodontal bacteria count
Time Frame: Baseline (T0), 1 month later (T1)
Comparison of the number of total bacteria and pathogens of the interdental microbiota before (T0) and in interim analysis (T1) for evaluation of the minimum period of effectiveness, by interdental sampling, on 4 sites, pooled then analyzed by bacterial PCR.
Baseline (T0), 1 month later (T1)
Periodontal health analysis:plaque index
Time Frame: Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
Comparison of periodontal and oral clinical parameters (plaque index) before (T0), intermediate (T1) and after (T2) introduction of einkorn into the diet, by sampling and periodontal analysis of all of the participants' teeth
Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
Periodontal health analysis: gingival index
Time Frame: Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
Comparison of periodontal and oral clinical parameters (gingival index) before (T0), intermediate (T1) and after (T2) introduction of einkorn into the diet, by sampling and periodontal analysis of all of the participants' teeth
Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
Periodontal health analysis : pocket depth and loss of clinical attachment
Time Frame: Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
Comparison of periodontal and oral clinical parameters (pocket depth and loss of clinical attachment) before (T0), intermediate (T1) and after (T2) introduction of einkorn into the diet, by sampling and periodontal analysis of all of the participants' teeth
Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
Periodontal health analysis : interdental inflammation
Time Frame: Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
Comparison of periodontal and oral clinical parameters (interdental inflammation) before (T0), intermediate (T1) and after (T2) introduction of einkorn into the diet, by sampling and periodontal analysis of all of the participants' teeth
Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
Periodontal health analysis : salivary pH
Time Frame: Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
Comparison of periodontal and oral clinical parameters (salivary pH) before (T0), intermediate (T1) and after (T2) introduction of einkorn into the diet, by sampling and periodontal analysis of all of the participants' teeth
Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
General health analysis : body mass index
Time Frame: Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
Comparison of general health indicators (body mass index) before (T0), intermediate (T1) and after (T2) introduction of einkorn in the diet, by a consultation and a general medical examination
Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
General health analysis : measurement of abdominal circumference
Time Frame: Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
Comparison of general health indicators (measurement of abdominal circumference) before (T0), intermediate (T1) and after (T2) introduction of einkorn in the diet, by a consultation and a general medical examination
Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
General health analysis : blood pressure
Time Frame: Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
Comparison of general health indicators (blood pressure) before (T0), intermediate (T1) and after (T2) introduction of einkorn in the diet, by a consultation and a general medical examination
Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
General health analysis : MOS SF-36 quality of life questionnaire
Time Frame: Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
Comparison of general health indicators (MOS SF-36 quality of life questionnaire) before (T0), intermediate (T1) and after (T2) introduction of einkorn in the diet, by a consultation and a general medical examination
Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
General health analysis : eating habits
Time Frame: Baseline (T0), 1 month later (T1), 3 months after baseline (T2)
Comparison of general health indicators (eating habits) before (T0), intermediate (T1) and after (T2) introduction of einkorn in the diet, by a consultation and a general medical examination
Baseline (T0), 1 month later (T1), 3 months after baseline (T2)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • Murat-Ringot A,Lan R,Fraticelli L,Fayet Y,Bourgeois D,Nugem R,Piton M,Goetz E,Préau M,Dutertre F,Bernoud-Hubac N,Basbous L,Lastmann A,Charreyre MT,Carrouel F

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 13, 2025

Primary Completion (Actual)

February 24, 2025

Study Completion (Actual)

May 27, 2025

Study Registration Dates

First Submitted

March 1, 2024

First Submitted That Met QC Criteria

March 14, 2024

First Posted (Actual)

March 18, 2024

Study Record Updates

Last Update Posted (Actual)

February 20, 2026

Last Update Submitted That Met QC Criteria

February 18, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Study Data/Documents

  1. results
    Information comments: https://pubmed.ncbi.nlm.nih.gov/39458490/

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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