Gut bacteria blend put to the test against low mood

NCT ID NCT06905223

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Sep 17, 2026 · Last updated Sep 18, 2026 · Updated 1 time

Summary

Researchers are testing whether a daily synbiotic formula called MQU10 can improve mood and well-being in adults with mild to moderate depressive symptoms. The formula combines 20 billion CFU of food-grade probiotic strains with prebiotic compounds. Thirty adults aged 18 and older with mild symptoms take the supplement, and clinicians rate their improvement over six weeks using standard mood scales. The study also tracks safety and how participants rate their own change.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
a synbiotic blend of probiotic strains and prebiotic compounds
What this could lead to
If it works, this could point toward a low-risk, food-based supplement that helps lift mood in people with mild depressive symptoms.
What could go wrong
This is a small pilot study of 30 people, so any hint of benefit could be chance and may not hold up in larger trials. Supplements can also cause digestive upset, and they are not a substitute for proven depression care.

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

About 30 people

The number the study aims to enrol. It can still change while the study runs.

Started

Apr 2025

Expected to finish

Sep 2027

An estimate. End dates often move.

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show 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: * Individuals aged 18 or above * Patient Health Questionnaire-9 (PHQ-9) score between 5 to 14 * Literate and can complete the self-report questionnaires * Able to understand the consent and sign the informed consent form Exclusion Criteria: * Current diagnosis of substance abuse or dependence; * A current or past history of bipolar disorder, manic or hypomanic episodes, schizophrenia, personality disorder, posttraumatic stress disorder (PTSD), intellectual disability, neurodegenerative disorders (e. g, Parkinson's disease) or organic mental disorder * Requiring immediate psychiatric care (e. g, imminently suicidal subjects) or have attempted suicide in the past 3 months * Use of antipsychotics, antidepressants or sedatives, unless on a stable dose in the last 4 weeks * History of severe organ failure, renal failure on dialysis, HIV infection * Active malignancy within 5 years * History of major surgery on the gastrointestinal tract, except cholecystectomy and appendectomy in the past 5 years * Night shift work * History of antibiotic use within 4 weeks * History of allergy to probiotics or lactose leading to a severe allergic reaction * Known pregnancy or lactating

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Conditions

The condition(s) this trial relates to.

Depression

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • GenieBiome Limited

    Hong Kong, Hong Kong

  • Healthymind Centre

    Hong Kong, Hong Kong

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