A Probiotic Blend Reduces Gastrointestinal Symptoms and Positively Impacts Microbiota Modulation in a Randomized Study
Study Details
Study Description
Brief Summary
This randomized, placebo-controlled, double-blind study will determine the effect of daily supplementation with a probiotic blend in 60 apparently healthy men and women recruited at a single investigational center in Northeast Ohio (i.e., The Center for Applied Health Sciences).
Subjects will attend three study visits. During Visit 1, subjects will be screened for participation [i.e., medical history, routine blood work, background baseline diet]. During Visits 2 and 3 subjects will complete questionnaires that assess their gastrointestinal health (e.g., abdominal discomfort/bloating, constipation, regularity, stool consistency). Visits 2 and 3 will correspond to before (week 0) and after six weeks of supplementation, respectively, with the probiotic dietary supplement or placebo.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Placebo Comparator: Placebo Consists of 575 mg rice oligodextrin |
Dietary Supplement: 575mg [30 billion colony forming units] probiotic blend of Bifidobacterium breve, Lactobacillus acidophilus, Lacticaseibacillus rhamnosus, Saccharomyces boulardii, and alpha amylase
A multi-strain probiotic blend
|
| Active Comparator: Active Consists of 575mg [30 billion colony forming units probiotic blend of Bifidobacterium breve 19bx, Lactobacillus acidophilus 16axg, Lacticaseibacillus rhamnosus 18fx, Saccharomyces boulardii 16mxg, and alpha amylase |
Dietary Supplement: 575mg [30 billion colony forming units] probiotic blend of Bifidobacterium breve, Lactobacillus acidophilus, Lacticaseibacillus rhamnosus, Saccharomyces boulardii, and alpha amylase
A multi-strain probiotic blend
|
Outcome Measures
Primary Outcome Measures
- Flatulence (gas) [Change from baseline to 6 weeks.]
Flatulence (gas) as measured by a 10 cm visual analogue scale, where higher values represent greater flatulence.
- Gastro-intestinal bloating [Change from baseline to 6 weeks.]
Gastro-intestinal bloating as measured by a 10 cm visual analogue scale, where higher values represent greater bloating.
- Abdominal discomfort [Change from baseline to 6 weeks.]
Abdominal discomfort as measured by a 10 cm visual analogue scale, where higher values represent greater discomfort.
- Gastrointestinal Symptom Rating Scale (GSRS) [Change from baseline to 6 weeks.]
Gastrointestinal problems as measured by the GSRS questionnaire, where higher values represent increased severity of gastrointestinal problems.
Secondary Outcome Measures
- Stool consistency [Change from baseline to 6 weeks.]
Stool consistency as measured by a 10 cm visual analogue scale, where higher values represent harder stools.
- Stool regularity [Change from baseline to 6 weeks.]
Stool regularity as measured by a 10 cm visual analogue scale, where higher values represent more regular stools.
- Constipation [Change from baseline to 6 weeks.]
Constipation as measured by a 10 cm visual analogue scale, where higher values represent more greater constipation.
Other Outcome Measures
- Short Form Health Survey (SF-36) [Change from baseline to 6 weeks.]
Health status as measured with the SF-36 questionnaire, where scores range from 0 to 100, and higher values represent better health status.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
all participants were required to be between 30-60yr
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score ≥12 on the GSRS
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have a body mass ≥120 pounds (54.5kg)
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body mass index (BMI) between 20.0-34.99kg/m2
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normotensive (<140/<90mmHg)
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normal resting heart rate (<90bpm)
Exclusion Criteria:
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Female participants who were pregnant or nursing
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history of unstable or new-onset cardiovascular or cardiorespiratory disease;
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stroke, diabetes, or other endocrine disorder;
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use of any nutritional supplement known to alter the gut microbiota/microflora;
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use of probiotic supplements or prebiotic supplements in the previous 4 weeks and for the duration of the study;
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use of any antibiotics, antifungals, antivirals, or antiparasitic within 8 weeks of the start of the study or throughout the study;
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any changes in diet within 4 weeks of study start date or throughout study duration;
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if the participant was unwilling to abstain from gut altering supplements for the study;
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malignancy in the previous 5yr except for non-melanoma skin cancer (basal cell cancer or squamous cell cancer of the skin);
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prior gastrointestinal bypass surgery (i.e., Lapband);
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any known gastrointestinal or metabolic diseases that might impact nutrient absorption or metabolism [e.g. short bowel syndrome, diarrheal illnesses, history of colon resection, gastroparesis, Inborn-Errors-of-Metabolism (such as PKU)];
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any chronic inflammatory condition/disease (e.g. rheumatoid arthritis, Crohn's disease, ulcerative colitis, Lupus, HIV/AIDS, etc.);
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known sensitivity to any ingredient in the test formulations as listed in the certificates of analysis.
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currently participating in another research study with an investigational product or had participated in another research study in the past 30 days
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any other diseases/conditions that, in the opinion of the medical staff, could confound the primary endpoints or place the subject at increased risk of harm if they were to participate.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | The Center for Applied Health Sciences | Canfield | Ohio | United States | 44406 |
Sponsors and Collaborators
- The Center for Applied Health Sciences, LLC
- Biohm Health, LLC
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 21-CAHS-102