Clinical trial Recruiting at 1 site Interventional Ages 45 to 80

Mushroom powder to slow cognitive decline in middle-aged and younger seniors

Official title: Study Protocol: The Efficacy of Mushroom to Reduce Cognitive Decline in At-Risk Middle-aged Adults and Young-olds Living in the Community

Run by National University of Singapore · NCT07775833 · Data updated 2026-11-12

A randomized trial will test whether daily golden oyster mushroom powder helps maintain cognitive function in adults aged 45–80 who have a family history of dementia or subjective memory concerns.

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Quick facts

Study typeInterventional
Ages45 Years to 80 Years
SexAll
Enrollment600 (estimated)
SponsorNational University of Singapore
Academic / other
Locations1 site (Singapore)
StatusRecruiting
StartedOctober 2026
Main results expectedDecember 2028
Study endsDecember 2030
Registry record updatedSeptember 1, 2026
Trial IDNCT07775833 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are community-dwelling adults 45–80 with a family history of dementia or subjective cognitive decline, who rarely consume mushrooms and have no dementia.

Probably not a fit

Participants with established neurological or psychiatric disorders, gout or hyperuricemia, significant sensory/motor impairments, or mushroom allergies may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized, controlled study enrolls about 600 community-dwelling adults aged 45–80 who do not have dementia and who use mushrooms infrequently. Participants are assigned to receive daily Pleurotus citrinopileatus mushroom powder for 24 months or a control condition, with outcomes focusing on cognitive function. Eligible individuals have a family history of Alzheimer's disease or self-reported worsening memory, and must not have major neurological or psychiatric conditions. The trial is conducted at a Singapore site led by the National University of Singapore. The goal is to determine if regular mushroom intake can help preserve cognitive performance over two years.

Why it matters

Potential benefit: If successful, daily mushroom supplementation could help maintain or slow cognitive decline in at-risk adults.

How similar studies have gone: Prior studies in similar areas have produced mixed results; this trial is based on exploratory evidence and aims to provide more definitive data.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* (1) Community-living adult aged 45 years to 80 years, AND
* (2) Family history of Alzheimer's disease or having subjective cognitive (SCD) defined as "self-reported memory problems that have been getting worse over the past year.", AND
* (3) Consume mushrooms no more than once a week, AND
* (4) No dementia: CDR global score equal to zero.

Exclusion Criteria:

* (1) Any diagnosis of neurological diseases (e.g., epilepsy, stroke) made by a clinician, OR
* (2) Any diagnosis of psychiatric illnesses (e.g., depressive disorders) made by a clinician, OR
* (3) Significant sensory or motor impairments, OR
* (4) Known allergy to mushrooms or a history of serious food allergies, OR
* (5) Participants with a history of gout, OR
* (6) Diagnosed with hyperuricemia.

Where it's running

  • Tahir Foundation Building, MD1, Level 12 (12 Science Drive 2)
    Singapore, Singapore
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.