Gut feeling: probiotic shows promise for easing anxiety and depression
NCT ID NCT07353320
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a probiotic called Weizmannia coagulans BC99 can reduce symptoms of anxiety and depression in stressed adults. 79 people took either the probiotic or a placebo for 8 weeks. Researchers measured changes using standard depression and anxiety rating scales. The goal was to see if improving gut bacteria could boost mental health.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Weizmannia coagulans BC99 (a probiotic)
- What this could lead to
- If it works, this could point toward a simple, natural supplement to help manage mild anxiety and depression.
- What could go wrong
- This is a small, early-stage trial with only 79 people. The effect may be small or no better than placebo, and results may not apply to everyone with anxiety or depression.
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
-
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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79 people
The number who actually took part.
- Started
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Apr 2024
- Finished
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Apr 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
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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18 to 65 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: 1. Adults aged 18-65 years. 2. Individuals experiencing scientific research, employment-related, or occupational stress, including graduate students or community-dwelling adults with job-related pressure. 3. A Hamilton Depression Rating Scale (HAMD-17) score ≥ 8 and/or a Hamilton 4) Anxiety Rating Scale (HAMA-14) score ≥ 7 at screening. 5)Ability and willingness to voluntarily participate in the study and to provide written informed consent prior to enrollment. Exclusion Criteria: 1. A confirmed previous diagnosis of other psychiatric disorders, including intellectual disability, bipolar disorder, treatment-resistant depression, or suicidal ideation. 2. Pregnant or breastfeeding women. 3. Individuals with known food or drug allergies, or those with alcohol abuse or psychotropic substance abuse. 4. Use of antibiotics or probiotics known to affect gut microbiota for more than one week within one month prior to enrollment. 5. Participants who withdrew from the study, discontinued intervention, or were unable to complete the study for any reason.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Henan University of Science and Technolog
Luoyang, Henan, 462000, China
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