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Influence of a Delivery System on the Efficacy of a Probiotic Intervention

Influence of a Delivery System on the Efficacy of a Probiotic Intervention

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01399996
Enrollment
36
Registered
2011-07-22
Start date
2012-04-30
Completion date
2014-08-31
Last updated
2023-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delayed Transit Time, Irregular Bowel Function

Keywords

probiotic, microbiota, transit time, immunity, immune function, constipation, bowel function

Brief summary

In the proposed work we will evaluate the efficacy of a probiotic bacterium (Bifidobacterium animalis subsp. lactis BB12) delivered in a yogurt smoothie (organism to be added before or after fermentation) or as a supplement (tablet) by assessing 1) bowel habits (transit time); 2) the ecology of the bacterial community in the GIT; and 3) immune status of healthy human volunteers. In addition to providing information about the relative efficacy of the delivery vehicles on probiotic function it will provide novel information about the influence of the yogurt smoothie alone (control) on all the parameters measured.

Detailed description

Probiotics (health-promoting bacteria) are often considered functional ingredients that act independently of the matrix used to deliver them to the human host. This thinking ignores the impact the delivery matrix (food or dietary supplement) may have on both the physiology of the probiotic organism and on the human host and is likely not true. Historically the most common probiotic foods have been fermented dairy products, particularly yogurts. Since yogurts are commonly understood to contain live good bacteria they are well accepted by consumers. However, increasingly over the last decade, probiotics are being added to non-dairy-based foods (juice, chocolate, cookies, etc) or consumed as supplements (tablets/capsules). While this expands the options for people to obtain probiotic organism, it is not clear whether probiotics delivered in these products are as efficacious as when delivered in a dairy food. In fact, the buffering capacity and nutrient composition of milk products may directly influence efficacy of the probiotic by increasing survival during passage through the gastrointestinal tract (GIT) and by modifying the physiology of the probiotic organism. In addition, fermentation products produced by the probiotic during manufacture of yogurt may also have an influence on the efficacy of probiotic bacteria. Our hypotheses are: 1. The vehicle used to deliver probiotic bacteria into the body influences the performance of the probiotic in vivo. Specifically, consumption of yogurt-based smoothie containing probiotic bacteria will result in greater decrease in fecal transit time, and have a greater effect on the composition of the fecal microbiota and on markers of immune status than the same probiotic bacteria delivered at the same level in the form of a dietary supplement (tablet). 2. Timing of the addition of probiotic organism to the yogurt smoothie (pre or post fermentation) will not change the efficacy of the probiotic with respect to the outcomes being assessed.

Interventions

DIETARY_SUPPLEMENTYogurt smoothie without probiotic

A daily 8 oz (240 mg) serving will provide 10x\^y5 cfu/ml of the probiotic (Bifidobacterium animalis subsp. lactis BB12).

DIETARY_SUPPLEMENTYogurt smoothie with probiotic added post fermentation

A daily 8 oz (240 mg) serving will provide 10x\^y5 cfu/ml of the probiotic (Bifidobacterium animalis subsp. lactis BB12).

DIETARY_SUPPLEMENTYogurt smoothie with probiotic added pre-fermentation

A daily 8 oz (240 mg) serving will provide 10x\^y5 cfu/ml of the probiotic (Bifidobacterium animalis subsp. lactis BB12).

DIETARY_SUPPLEMENTA capsule containing the probiotic

A capsule taken daily will provide between 10x\^y9 and 10x\^y10 cfu/ml of the probiotic (Bifidobacterium animalis subsp. lactis BB12).

Sponsors

Dairy Management Inc.
CollaboratorINDUSTRY
Penn State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Generally healthy * Men and women * 18-40 years of age * Body mass index between 20 and 35 kg/m\^2 * Persons with irregular bowel function as determined using the Rome III criteria (1) which is used to classify functional gastrointestinal disorders. * Increased gastrointestinal transit time \> 60 hours.

Exclusion criteria

* Smoking and/or use of other tobacco products * Blood pressure greater than 140/90 mm Hg * A history of myocardial infarction, stroke, diabetes mellitus, liver disease, kidney disease and thyroid disease (unless controlled by medication and blood results within the previous 6 months are provided). * Lactation, pregnancy or desire to become pregnant during the study * Use of cholesterol-lowering medication * Refusal to discontinue intake of putative cholesterol-lowering supplements (psyllium, fish oil capsules, soy lecithin, niacin, fiber, flax, phytoestrogens, stanol/sterol supplemented foods * Refusal to discontinue probiotics,nutritional supplements, herbs or vitamins * Vegetarianism/Veganism * Lactose intolerance * Clinical diagnosis of Inflammatory Bowel Disease (IBD), e.g. Crohn's Disease or ulcerative colitis * Excessive alcohol consumption (\> 14 standard drinks per week) * Chronic use of anti-inflammatory medications (unless able to discontinue) * Individuals taking stool softeners or enemas on a regular basis. * Allergy to polyvinyl chloride (PVC) or any other type of plastic * Individuals with a bowel transit time of \< 60 hours at time of screening * Individuals with swallowing disorders or dysphagia to food or pills * Suspected strictures, fistulas, or physiological GI Obstruction * GI surgery within the past three months * Refusal to agree to give blood or plasma for the length of the study. Note: If a participant experiences a delay in passing the capsule (beyond five days) they will be treated accordingly and excluded from future participation in the study.

Design outcomes

Primary

MeasureTime frameDescription
Gastrointestinal transit timeWeeks 4, 10, 16, 22Gastrointestinal transit time is the amount of time it takes for food to travel through the digestive tract to be excreted. It will be measured using the SmartPill wireless motility capsule.

Secondary

MeasureTime frame
Change from baseline in the fecal microbiota profile at 4 weeks following each of the 4 interventions and 1 free living periodWeeks 4, 10, 16, 22 and 28
Change from baseline in immune status at 4 weeks following each of the 4 interventions and 1 free living periodWeeks 4, 10, 16, 22, 28

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026