Actively Recruiting
Effect of ExoBDNF Lactic Acid Bacteria Supplement on Cognitive Functions, Sleep and Psychological
Led by SunWay Biotech Co., LTD. · Updated on 2025-11-24
50
Participants Needed
1
Research Sites
32 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This open-label, single-group, pre/post-test clinical study was conducted to investigate whether ExoBDNF probiotic supplementation could improve cognitive ability. It is expected that 40 subjects aged 18 years and above will be recruited, with a target of 30 cases, to take ExoBDNF probiotics for a total of 8 weeks.
CONDITIONS
Official Title
Effect of ExoBDNF Lactic Acid Bacteria Supplement on Cognitive Functions, Sleep and Psychological
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Subjects must be volunteers who are 18 years of age or older, mentally clear and able to communicate.
- Subjects who agree to participate in this trial and voluntarily sign the trial consent form.
You will not qualify if you...
- Subjects who are expected to be or have been confirmed to be pregnant (medical history).
- Subjects with gallbladder disease, gastrointestinal disease, gout, porphyria, or a history of gastric weight control surgery.
- Subjects with high blood pressure ( 60/100 mmHg after resting for 10 minutes) or taking diuretics.
- Subjects with heart disease, hepatorenal insufficiency, hyperthyroidism or hypothyroidism, Cushing's syndrome, malignant tumors, or any other disease that may affect the results of the study.
- Subjects with severe hearing or visual impairment that makes it impossible to perform examinations and assessments.
- Subjects with any history of brain surgery, penetrating, neurovascular, infectious or other severe brain injury, epilepsy or other major neurological abnormalities, such as traumatic brain injury with loss of consciousness for more than 24 hours, or memory loss after head trauma for more than 7 days were excluded.
- Subjects with intellectual disabilities.
- Subjects who had consumed probiotics or were expected to consume probiotics within 2 weeks before the screening visit.
- Subjects who had participated in or were expected to participate in clinical trials within 4 weeks before the screening visit.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Tri-Service General Hospital, National Defense Medical Center
Taipei, Taiwan
Actively Recruiting
Research Team
S
Sean Lin
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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