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Healthy Effects of an Innovative Probiotic Pasta (SFLABPASTA)

Primary Purpose

OBESITY, INFLAMMATION, DYSLIPIDEMIA

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
whole grain pasta
Sponsored by
University of Parma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for OBESITY

Eligibility Criteria

30 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Overweight / Obesity
  • Lower consumers of fruit and vegetables

Exclusion Criteria:

  • Antibiotic treatment within 3 months prior the pasta feeding
  • Chronic diseases
  • Surgeries
  • Consumer of whole grain products
  • Dieting
  • Pregnant or lactating

Sites / Locations

  • University of Parma - Department of Food Sciences
  • University of Parma

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Control pasta

Probiotic Whole Grain Pasta

Arm Description

Volunteers were fed with control pasta, without B-glucans and spores of B. coagulans once a day for 12 weeks.

Volunteers were fed with probiotic fortified pasta, including B-glucans and spores of B. coagulans once a day for 12 weeks.

Outcomes

Primary Outcome Measures

Variation of plasma lipids
Measure of plasma concentrations (mg/dL) of Total-, LDL-, and HDL-Cholesterol; Measure of plasma concentrations (µg/mL) of Non Esterified Fatty Acids (NEFA), Esterified Fatty Acids (EFA) and Short Chain Fatty Acids (SCFA). Statistical analysis of the primary outcome was performed within and between each single intervention-arm. Further, a post-hoc subdivision of the study participants by means of a BMI or glycaemia cut-off value was applied, and statistical differences of the primary outcome have been considered.
Variation of fecal microbiota composition
By FISH (colony-forming unit, CFU/g). Statistical analysis of the primary outcome was performed within and between each single intervention-arm. Further, a post-hoc subdivision of the study participants by means of a BMI or glycaemia cut-off value was applied, and statistical differences of the primary outcome have been considered.
Variation of antioxidant activity on fecal waters
Measure of fecal waters FRAP (µmol/L) and TEAC (µmol/L) concentrations. Statistical analysis of the primary outcome was performed within and between each single intervention-arm. Further, a post-hoc subdivision of the study participants by means of a BMI or glycaemia cut-off value was applied, and statistical differences of the primary outcome have been considered.

Secondary Outcome Measures

Variation of body weight
Measure of body weight (kg).
Variation of serum inflammatory marker concentration
Measure of serum IL-2, IL-4, IL-5, IL-6, IL-10, IL-12, IFN-γ,TNF-α, PAI-1, Ghrelin, Leptin, Visfatin, Resistin concentrations (pg/mL). Statistical analysis of the secondary outcome was performed within and between each single intervention-arm. Further, a post-hoc subdivision of the study participants by means of a BMI or glycaemia cut-off value was applied, and statistical differences of the secondary outcome have been considered.
Variation of blood pressure
Measure of blood pressure (mmHg). Statistical analysis of the secondary outcome was performed within and between each single intervention-arm. Further, a post-hoc subdivision of the study participants by means of a BMI or glycaemia cut-off value was applied, and statistical differences of the secondary outcome have been considered.
Variation of body circumferences
Measure of waist and hip circumferences (mm). Statistical analysis of the secondary outcome was performed within and between each single intervention-arm. Further, a post-hoc subdivision of the study participants by means of a BMI or glycaemia cut-off value was applied, and statistical differences of the secondary outcome have been considered.
Variation of urine antioxidant marker
Measurement of betaine in urine (mmol/L). Statistical analysis of the secondary outcome was performed within and between each single intervention-arm. Further, a post-hoc subdivision of the study participants by means of a BMI or glycaemia cut-off value was applied, and statistical differences of the secondary outcome have been considered.

Full Information

First Posted
July 26, 2014
Last Updated
October 30, 2018
Sponsor
University of Parma
Collaborators
Universita di Verona
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1. Study Identification

Unique Protocol Identification Number
NCT02236533
Brief Title
Healthy Effects of an Innovative Probiotic Pasta
Acronym
SFLABPASTA
Official Title
Healthy Effects of an Innovative Probiotic Pasta
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
March 2014 (undefined)
Primary Completion Date
September 2014 (Actual)
Study Completion Date
March 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Parma
Collaborators
Universita di Verona

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of the project was the evaluation of the antioxidant and anti-inflammatory effects of a whole grain pasta, enriched in barley β-glucans and fortified with strains of Bacillus coagulans, versus a control wheat pasta on healthy volunteers, using a parallel randomized controlled trial.
Detailed Description
Epidemiological evidences indicate that consumption of whole grains products is associated to a decreased risk for common chronic diseases, as cardiovascular diseases, diabetes, obesity, hypertension and metabolic syndrome. In the present study a whole grain pasta was supplemented with prebiotics and probiotics 'ad hoc' formulated. In detail, pasta was industrially developed after the identification of particular cultivars of wheat and barley, rich in carotenoids, β-glucans (2.6 g/100g pasta), not soluble fibers and antioxidants. Further, pasta was supplemented with spores of Bacillus coagulans, a putative probiotic microorganism, belonging to Lactobacillus family. It is well demonstrated the ability of this microorganism to survive to technological processes and to upper gastro-intesinal tract, in order to exert beneficial effects in the lower gut, as anti-microbial activity, increasing immunological defences as well as improvements in intestinal regularity. Conversely, the control pasta was made from the same cultivar of grain and by the same technological process, but without any supplementation. In this parallel randomized controlled one arm trial, 40 healthy volunteers were randomly allocated for the consumption of the two kind of pasta once a day, for 12 weeks. At the beginning of the study and every 4 weeks, subjects were asked to provide blood, urine and feces for the evaluation of: blood inflammation markers; blood lipid and carbohydrate profile; blood and urine markers of cardiovascular risk; feces profile of microbiota and detection of markers for the healthiness of the gut. In addition, volunteers filled in different questionnaires regarding their dietary habits, the physical activity and the gut healthiness.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
OBESITY, INFLAMMATION, DYSLIPIDEMIA, CONSTIPATION

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control pasta
Arm Type
Placebo Comparator
Arm Description
Volunteers were fed with control pasta, without B-glucans and spores of B. coagulans once a day for 12 weeks.
Arm Title
Probiotic Whole Grain Pasta
Arm Type
Experimental
Arm Description
Volunteers were fed with probiotic fortified pasta, including B-glucans and spores of B. coagulans once a day for 12 weeks.
Intervention Type
Dietary Supplement
Intervention Name(s)
whole grain pasta
Intervention Description
Volunteers were fed with probiotic fortified pasta or control pasta once a day for 12 weeks.
Primary Outcome Measure Information:
Title
Variation of plasma lipids
Description
Measure of plasma concentrations (mg/dL) of Total-, LDL-, and HDL-Cholesterol; Measure of plasma concentrations (µg/mL) of Non Esterified Fatty Acids (NEFA), Esterified Fatty Acids (EFA) and Short Chain Fatty Acids (SCFA). Statistical analysis of the primary outcome was performed within and between each single intervention-arm. Further, a post-hoc subdivision of the study participants by means of a BMI or glycaemia cut-off value was applied, and statistical differences of the primary outcome have been considered.
Time Frame
12 weeks
Title
Variation of fecal microbiota composition
Description
By FISH (colony-forming unit, CFU/g). Statistical analysis of the primary outcome was performed within and between each single intervention-arm. Further, a post-hoc subdivision of the study participants by means of a BMI or glycaemia cut-off value was applied, and statistical differences of the primary outcome have been considered.
Time Frame
12 weeks
Title
Variation of antioxidant activity on fecal waters
Description
Measure of fecal waters FRAP (µmol/L) and TEAC (µmol/L) concentrations. Statistical analysis of the primary outcome was performed within and between each single intervention-arm. Further, a post-hoc subdivision of the study participants by means of a BMI or glycaemia cut-off value was applied, and statistical differences of the primary outcome have been considered.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Variation of body weight
Description
Measure of body weight (kg).
Time Frame
12 weeks
Title
Variation of serum inflammatory marker concentration
Description
Measure of serum IL-2, IL-4, IL-5, IL-6, IL-10, IL-12, IFN-γ,TNF-α, PAI-1, Ghrelin, Leptin, Visfatin, Resistin concentrations (pg/mL). Statistical analysis of the secondary outcome was performed within and between each single intervention-arm. Further, a post-hoc subdivision of the study participants by means of a BMI or glycaemia cut-off value was applied, and statistical differences of the secondary outcome have been considered.
Time Frame
12 weeks
Title
Variation of blood pressure
Description
Measure of blood pressure (mmHg). Statistical analysis of the secondary outcome was performed within and between each single intervention-arm. Further, a post-hoc subdivision of the study participants by means of a BMI or glycaemia cut-off value was applied, and statistical differences of the secondary outcome have been considered.
Time Frame
12 weeks
Title
Variation of body circumferences
Description
Measure of waist and hip circumferences (mm). Statistical analysis of the secondary outcome was performed within and between each single intervention-arm. Further, a post-hoc subdivision of the study participants by means of a BMI or glycaemia cut-off value was applied, and statistical differences of the secondary outcome have been considered.
Time Frame
12 weeks
Title
Variation of urine antioxidant marker
Description
Measurement of betaine in urine (mmol/L). Statistical analysis of the secondary outcome was performed within and between each single intervention-arm. Further, a post-hoc subdivision of the study participants by means of a BMI or glycaemia cut-off value was applied, and statistical differences of the secondary outcome have been considered.
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Overweight / Obesity Lower consumers of fruit and vegetables Exclusion Criteria: Antibiotic treatment within 3 months prior the pasta feeding Chronic diseases Surgeries Consumer of whole grain products Dieting Pregnant or lactating
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nicoletta Pellegrini, Professor
Organizational Affiliation
University of Parma
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Parma - Department of Food Sciences
City
Parma
State/Province
PR
ZIP/Postal Code
43124
Country
Italy
Facility Name
University of Parma
City
Parma
ZIP/Postal Code
43124
Country
Italy

12. IPD Sharing Statement

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Healthy Effects of an Innovative Probiotic Pasta

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