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Gut check: army tests if probiotics shield soldiers from stress
NCT ID NCT05392556
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether taking a probiotic or prebiotic supplement for four weeks could reduce the negative effects of acute stress on the gut and brain. Seventy-three healthy adults were randomly assigned to receive a probiotic, a prebiotic, or a placebo. They underwent physical and mental stress tests, including a weighted treadmill walk and a challenging decision-making task with mild electric shocks. Researchers measured changes in gut permeability, stress hormones, heart rate, and cognitive performance.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Probiotic (Cerebiome with Bifidobacterium longum and Lactobacillus helveticus) and prebiotic (Bimuno-GOS)
- What this could lead to
- If successful, this could point toward dietary supplements that help protect gut and brain function during stressful situations.
- What could go wrong
- This is a small, early-stage study in healthy adults, not patients. Results may not apply to real-world stress or lead to any practical treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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73 people
The number who actually took part.
- Started
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Jul 2022
- Finished
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Oct 2025
- Lead sponsor
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A government agency
The lead sponsor is a US federal agency other than the NIH.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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17 to 39 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Men and women aged 18 - 39 years (active duty personnel who are 17 yr of age will also be allowed to participate). * In good health as determined by Medical Clearance. * Physically active: If military, passed most recent record Combat or Physical Fitness Test, and ≥4 d/wk aerobic and/or resistance exercise. If civilian, ≥4 d/wk aerobic and/or resistance exercise. * Meet Army weight for height and body composition standards as defined in Army Regulation 600-9: * Self-reports ≥4 bowel movements/week. * Self-reports normal hearing. * Willing to maintain usual diet until provided diet phase of study. Exclusion Criteria: * Pregnant, expecting to become pregnant during study, or breastfeeding. * Abnormal menstrual cycles \[i.e., not between 26-32 days in duration; or not 5-6 menstrual cycles within the past 6 months\], or those that have had an IUD placed within the last month or removed within the past 3 months. * Less than 20/20 acuity on the Snellen eye chart of normal or corrected-to-normal acuity. * Any of the following medical conditions: Neurological or psychological disorder (such as depression, anxiety disorders, migraines, cluster headaches, seizures, post-traumatic stress disorder or panic attacks). Cardiac disease (including arrhythmia or fast or skipped heart beats) Hypertension Has a pacemaker Insomnia Musculoskeletal injuries that compromise exercise capability Metabolic or cardiovascular abnormalities (e.g., kidney disease, diabetes, etc.) Disease of the GI tract including, but not limited to diverticulitis, inflammatory bowel disease, irritable bowel syndrome, peptic ulcer disease, Crohn's disease, and ulcerative colitis Excessive alcohol use or other substance abuse issues Immunodeficiency disorder Allergy to skin adhesive * Colonoscopy within 3 months of study participation. * Any use of antibiotics or antimycotics, except topical antibiotics/antimycotics, within 3 months of study participation. * Regular use of over-the-counter medications (including antacids, laxatives, stool softeners, and anti-diarrheals) unless approved by medical office and study PI. * Taking prescription medications other than a contraceptive (unless approved by medical office and study PI) * Not willing or able to refrain from using over the counter medications for 72hr before stress exposure days. * Not willing or able to stop consumption of dietary supplements at least 2 weeks before and throughout study participation. * Not willing or able to stop consumption of probiotic-containing foods (e.g., yogurt, etc.) or foods containing added prebiotics (e.g., inulin) at least 2 weeks before and throughout study participation. * Not willing to abstain from non-provided foods and beverages, including alcohol, during the controlled-diet period. * Not willing to abstain from caffeine and any nicotine containing products (smoking, chewing, vaping, etc.) during the week prior to stress exposure days. * Not willing to refrain from strenuous exercise for 24hr prior to stress exposure days. * Allergies, intolerances, unwillingness or inability to eat intervention supplements, or provided foods and beverages. * Following vegetarian/vegan diet or other highly restrictive diet (e.g., ketogenic diet, very high protein diet, Paleo diet). * Any previous blood donation, within 8 weeks of a study blood draw, of a volume that when combined with the amount of blood to be collected during the study would exceed 550 mL
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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United States Army Research Institute of Environmental Medicine
Natick, Massachusetts, 01760, United States
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