ClinicalTrials.Veeva

Menu

An Open Label Trial Evaluating the Efficacy of Lacticaseibacillus Paracasei PS23 on Cognition

C

Chi-Chang Huang

Status

Invitation-only

Conditions

Subjective Cognitive Decline (SCD)

Treatments

Dietary Supplement: Lacticaseibacillus paracasei

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT07168824
IRB-25-061-A2

Details and patient eligibility

About

This open label study aims to evaluate whether the consumption of probiotics can improve symptoms and overall quality of life in individuals experiencing cognitive decline symptoms, as well as to evaluate the effects of probiotics on blood-related biomarkers.

Full description

Lacticaseibacillus paracasei PS23 (PS23) is a specific strain of probiotic bacteria known for its potential health benefits, particularly in the context of aging and muscle health. Research suggests that it may improve cognitive function, reduce age-related muscle loss, and modulate the gut microbiota. Probiotic supplements like PS23 are being explored as potential therapeutic agents for age-related cognitive deficits. A prior study showed that PS23 supplementation delayed age-related cognitive decline in mice. Additionally, PS23 has shown antidepressant-like effects and has been found to enhance physical performance and promote muscle recovery following injury.

Enrollment

40 estimated patients

Sex

All

Ages

50 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults aged 50 to 85 years who self-report experiencing signs of cognitive decline.
  • No prior diagnosis of dementia or Alzheimer's disease (AD).
  • Willing and able to comply with study assessments and requirements, and provide written informed consent.

Exclusion criteria

  • Use of antibiotics or probiotic powder, capsules, or tablets within the past month.
  • Currently undergoing antibiotic treatment.
  • Known allergy to dairy products.
  • Presence of immunodeficiency or impaired immune function.
  • Diagnosis of small intestinal bacterial overgrowth (SIBO).
  • Determined unsuitable by the investigator, for example, initiation of any new medication or therapy during the study period, particularly those related to memory impairment or cognitive decline.

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

40 participants in 1 patient group

Probiotics
Experimental group
Description:
Lacticaseibacillus paracasei PS23 one capsule daily for 12 weeks
Treatment:
Dietary Supplement: Lacticaseibacillus paracasei

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems