CROMA: Fiber-enriched Croissant Consumption and Effects on Metabolic Status, Appetite and Gut Microbiota

Sponsor
Federico II University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04999280
Collaborator
(none)
32
1
2
16
2

Study Details

Study Description

Brief Summary

The aim of this study is to evaluate the effect of a daily consumption for 2 weeks of a sourdough croissant enriched with dietary fibers vs a control sourdough croissant with no fiber added on daily energy intakes, fasting metabolic parameters, inflammatory status, blood pressure, anthropometric measures, body composition, appetite sensations, gastrointestinal functionality and gut microbiota composition.

Condition or Disease Intervention/Treatment Phase
  • Other: Fiber Croissant (FIBCRO) Group
  • Other: Control Croissant (CONCRO) Group
N/A

Detailed Description

Associations between human health, diet and gut microbiota composition and functionality have been widely highlighted by the scientific literature in this field. Evidence shows that population adopting a Western dietary model, with a reduced intake of dietary fiber, undergo an adaptation of the gut microbiota characterized by the loss of some bacterial species and a general reduction in microbial biodiversity. The national guidelines for a healthy diet suggest to include daily fruit, vegetables, whole grains and legumes (the main sources of fiber in the diet) in the habitual diet to reduce the risk of diseases and to improve health. However, the compliance with these nutritional recommendations is generally low among individuals. Therefore, the commercial availability of dietary fiber-enriched products could be advantageous.

Breakfast is an important meal that should provide at least 20% of the daily calories with an adequate supply of all nutrients. Having fiber-enriched foods for breakfast could bring numerous nutritional benefits and if they are made with sourdough may be even better. Indeed, sourdough leavened baked products provide compounds with potential prebiotic activity, reduce the glucose and insulin response, increase satiety and reduce gastro-intestinal disorders upon consumption.

The hypothesis is that the combination of sourdough and dietary fiber in baked products could further ameliorate glucose metabolism in consumers compared to sourdough products.

The aim of this study is to evaluate the effects of a daily consumption at breakfast for 2 weeks of a sourdough croissant enriched with dietary fibers from 10 different sources vs a sourdough croissant with no fiber added (control) on daily energy intakes, metabolic and inflammatory status, appetite feelings, body weight, body mass index (BMI), waist and hip circumferences, body composition, blood pressure, gut microbiota composition and gastrointestinal functionality in healthy subjects.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
32 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Effect of Daily Consumption of a Fiber-enriched Croissant on Metabolic Status, Dietary Habits and Gut Microbiota in Healthy Subjects (CROMA)
Actual Study Start Date :
Apr 1, 2021
Anticipated Primary Completion Date :
Apr 30, 2022
Anticipated Study Completion Date :
Jul 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Fiber Croissant (FIBCRO) Group

Daily consumption at breakfast for 2 weeks of a fiber-enriched croissant

Other: Fiber Croissant (FIBCRO) Group
Subjects will consume for 2 weeks at breakfast a fiber-enriched sourdough croissant. All subjects will be requested not to change other dietary habits and their physical activity during the 2 week intervention period.
Other Names:
  • Fiber-enriched Croissant
  • Active Comparator: Control Croissant (CONCRO) Group

    Daily consumption at breakfast for 2 weeks of a control croissant

    Other: Control Croissant (CONCRO) Group
    Subjects will consume for 2 weeks at breakfast a sourdough croissant. All subjects will be requested not to change other dietary habits and their physical activity during the 2 week intervention period.
    Other Names:
  • Control Croissant
  • Outcome Measures

    Primary Outcome Measures

    1. Variation of daily energy intakes [2 weeks]

      Calculation of total daily energy intakes based on 7 days food records

    Secondary Outcome Measures

    1. Changes in fasting plasma inflammatory markers [2 weeks]

      Measure of plasma C-reactive protein (mmol/L)

    2. Changes in fasting plasma lipids [2 weeks]

      Measure of plasma concentrations (mg/dL) of Total-, LDL-, and HDL-Cholesterol, as well as Triglycerides

    3. Changes in fasting blood glucose [2 weeks]

      Measure of blood glucose concentrations (mg/dL)

    4. Variation of serum Insulin hormone concentration [2 weeks]

      Measure of serum Insulin concentrations (mg/dL)

    5. Variation of plasma endocannabinoids and N-acyl-ethanolamines concentration [2 weeks]

      Measure of plasma endocannabinoids and N-acyl-ethanolamines concentrations (mg/dL)

    6. Variation of serum dipeptidyl-dipeptidase-IV activity [2 weeks]

      Measure of serum dipeptidyl-dipeptidase-IV (U/L) activity

    7. Variation of urinary excretion levels of polyphenols [2 weeks]

      Measure of polyphenols concentration in urine by mean of liquid chromatography coupled with tandem mass spectrometry (LC/MS/MS)

    8. Variation of urinary excretion levels of urolithins [2 weeks]

      Measure of urolithins concentration in urine by mean of LC/MS/MS

    9. Changes in stool consistency [2 weeks]

      Measure of consistency of feces by mean of King's stool chart filled out by subjects. The chart comprises four categories of stool consistency: hard and formed, soft and formed, loose and unformed, liquid.

    10. Changes in stool weight [2 weeks]

      Measure of stool weight by mean of King's stool chart filled out by subjects. The chart comprises three categories of stool weight : <100 g, 100-200 g, >200 g.

    11. Changes in stool frequency [2 weeks]

      Measure of frequency of feces by mean of King's stool chart filled out by subjects. Fecal frequency is incorporated by recording the code of each feces passed over a 24 hour period.

    12. Changes in gastrointestinal functionality [2 weeks]

      Calculation of daily fecal score from summation of all scores for stool consistency, weight and frequency obtained from King's stool chart filled out by subjects. Scores are weighted such that an increase in fecal frequency alone results in a higher score than a change in fecal consistency alone, which in turn results in a higher score than an increase in fecal weight alone. Diarrhea is classified by a daily fecal score of 15 or more.

    13. Changes in faecal microbiome [2 weeks]

      The composition of faecal microbiome will be determined by high throughput sequencing of the ribosomal ribonucleic acid 16S (16S rRNA) gene. The massive number of sequences obtained will be analyzed by using state of the art bioinformatics tools and the presence and relative abundance of the microbial species occurring in each sample will be determined.

    14. Changes in body weight [2 weeks]

      Measure of body weight in fasting subjects

    15. Changes in body mass index [2 weeks]

      Calculation of body mass index by using the formula weight in kilograms divided by height in meters squared.

    16. Changes in waist circumference [2 weeks]

      Measure of waist circumference at the midpoint between the lower margin of the least palpable rib and the top of the iliac crest.

    17. Changes in hip circumference [2 weeks]

      Measure of hip circumference around the widest portion of the buttocks.

    18. Changes in blood pressure [2 weeks]

      Measure of systolic pressure and diastolic pressure in millimetres of mercury (mmHg) by using a digital sphygmomanometer

    19. Changes in body composition [2 weeks]

      Body composition 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.

    20. Variation of hunger feeling scores [2 weeks]

      Measures of hunger sensation over the day reported by subjects by using hunger Visual Analogue Scales (VAS) 0-10 centimeters (where 0 corresponds to the lowest and 10 to the highest feeling the individual could perceive). Changes in these scores may reflect potential effects of dietary intervention in modulating hunger.

    21. Variation of fullness feeling scores [2 weeks]

      Measure of fullness sensation over the day reported by subjects by using fullness Visual Analogue Scales (VAS) 0-10 centimeters (where 0 corresponds to the lowest and 10 to the highest feeling the individual could perceive). Changes in these scores may reflect potential effects of dietary intervention in modulating fullness.

    22. Variation of satiety feeling scores [2 weeks]

      Measure of satiety sensation over the day reported by subjects by using satiety Visual Analogue Scales (VAS) 0-10 centimeters (where 0 corresponds to the lowest and 10 to the highest feeling the individual could perceive). Changes in these scores may reflect potential effects of dietary intervention in modulating satiety.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 50 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • healthy subjects;

    • men and women;

    • age 18-50 years;

    • 20 kg/m2 ≤ BMI ≤ 35 kg/m2;

    • habitual daily breakfast consumption (≥ 250kcal/day);

    • habitual diet characterized by absence of any food supplements and alternative medication, probiotics and prebiotics, whole grain and/or fiber enriched foods;

    • intake of fruit/vegetables < 3 servings/day;

    • low level of physical activity;

    • signed written informed consent.

    Exclusion Criteria:
    • food allergies and intolerances and celiac disease;

    • gastrointestinal diseases;

    • relevant diseases;

    • pregnant or breastfeeding;

    • previous abdominal surgery;

    • hypertriglyceridemia (Triglycerides > 200 mg/dL);

    • hypercholesterolemia (Total cholesterol > 200 mg/dL);

    • hyperglycaemia (glycaemia ≥ 110 mg/dL);

    • hypertension (arterial blood pressure ≥140/90 mm Hg);

    • weight loss ≥ 3 kg within 2 months before the study;

    • antibiotics treatment within 3 months before the study;

    • any medication (different from antibiotics) at the enrollment and within 2 months before the study;

    • habitual diet characterized by high fruit and vegetables intakes (>3 portion/die);

    • high level of physical activity;

    • alcohol consumption ≥ 3 alcohol units per day;

    • simultaneous participation in other trial.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of Agricultural Sciences, Federico II University Portici Italy 80055

    Sponsors and Collaborators

    • Federico II University

    Investigators

    • Study Director: Paola Vitaglione, Professor, Department of Agricultural Sciences, Federico II University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Paola Vitaglione, Associate Professor, Federico II University
    ClinicalTrials.gov Identifier:
    NCT04999280
    Other Study ID Numbers:
    • CROMA
    First Posted:
    Aug 10, 2021
    Last Update Posted:
    Aug 16, 2021
    Last Verified:
    Aug 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 16, 2021