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Lion's mane supplement tested for brain boost in healthy women

NCT ID NCT07405632

Symptom relief Sponsor: University of Social Sciences and Humanities, Warsaw Source: ClinicalTrials.gov ↗

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
Running, but no longer taking on new participants.
Completed This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether taking Lion's Mane mushroom extract daily for two months can improve memory and attention in healthy, working women aged around 40-60. Participants took either the extract or a placebo pill and completed thinking and memory tests at several points. The goal was to see if this natural supplement could help sharpen cognitive function.

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

85 people

The number who actually took part.

Started

Jan 2025

Finished

Oct 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

30 to 50 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: \- residing in Warsaw, Poland or the surrounding area. Exclusion Criteria: * pregnancy or lactation, * history of head injury with neurological consequences, * history of neurological disorders or diseases, * chronic use of antibiotics, * use of antibiotics within the last 30 days, * chronic use of antifungal medications, * use of antifungal medications within the last 30 days, * allergies or intolerance to mushrooms (especially Lion's Mane), * consumption of caffeinated beverages (e.g., coffee, energy drinks) prior to the study visit.

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Conditions

The condition(s) this trial relates to.

attention deficit hyperactivity disorder, inattentive type

As listed by the trial registrant

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

Attention Cognitive function and well-being MEMORY

Contacts and locations

Locations

  • SWPS University

    Warsaw, Masovian Voivodeship, 03-815, Poland

More trials for these conditions

Other studies related to the condition(s) this trial covers.