Phosphatidylserine Improves Cognitive Function in the Elderly

Last updated: May 10, 2022
Sponsor: First Affiliated Hospital Xi'an Jiaotong University
Overall Status: Active - Not Recruiting

Phase

N/A

Condition

Aging

Treatment

N/A

Clinical Study ID

NCT04920305
XJTU1AF2021LSY-200
  • Ages 60-70
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

Cognitive decline is a common symptom of aging, and age-related cognitive impairments are considered normal or inevitable, especially in people over 60, whose memory is more likely to be affected by age. As life expectancy has increased, the number of people with age-related cognitive impairment has also increased. The improvement or slowing of cognitive impairment has received more attention. Phosphatide is a naturally occurring Phosphatide, but it is the main acidic phospholipid in the brain. Phosphatidylserine (PS) is a phospholipid that regulates the function of key proteins in cell membranes and can improve brain function and repair brain damage. PS is thought to enhance neuronal membrane function, which in turn enhances cognitive function. However, there are few studies on the effect of PS on human cognitive function, especially on the elderly, and the results are inconsistent. In this study, people aged 60-70 were given PS intervention for 6 months. Montreal Cognitive Assessment (MOCA) and Mini-Mental State Examination.MMSE) and head MRI are used to evaluate the cognitive function of the subjects before and after the intervention to observe the influence of PS on the cognitive function of the elderly, which is of certain significance for the accurate assessment of the cognitive function of the elderly population and the improvement of the cognitive function of the elderly.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Age 60 to 70, gender is not limited.

Exclusion

Exclusion Criteria:

  • Delirium, confusion, confusion of consciousness.
  • Alzheimer's disease, Parkinson's disease, stroke, cerebral hemorrhage, brain tumor,hydrocephalus.
  • Viral, fungal, and syphilis infections.
  • Sufferers from cerebrovascular disease (as demonstrated by a Hachinski ischemic score,or neuroimaging test).
  • Repeated mild head trauma, or head trauma resulting in loss of consciousness (morethan 1h).
  • Depression, mania, and other mental disorders.
  • Alcoholism and drug dependence.
  • The following diseases may lead to mental retardation: Kidney disease, respiratory system disease, heart disease, liver disease, uncontrolleddiabetes, endocrine, metabolic, blood disease, malignant disease, more than 2 years havenot been relieved.
  • Taken any medication that may cause psychosis or affect intelligence in the past 1month.
  • known allergy to phosphatidylserine or related ingredients.

Study Design

Total Participants: 100
Study Start date:
September 01, 2022
Estimated Completion Date:
December 31, 2023

Study Description

This is a randomized, controlled, double-blind clinical trial, in which 100 subjects were randomly assigned to the treatment group and the control group 1:1 by computer generated random numbers. Before start of the study, all the subjects underwent the first magnetic resonance (MR) and electroencephalogram (EEG) data collection. The working memory capacity of subjects in the N-back paradigm was measured (collected during the N-back task in the EEG test), and the cognition was measured by MOCA and MMSE. After the first data collection was completed, subjects in the treatment group oral the PS (600mg/d, q.d.) for 6 months. Subjects in the control group were given a placebo, which was the same shape of bean powder(600mg/d, q.d.). Under the supervision of nurses, all subjects took the additive at regular times daily. At the end of the 6-month additive trial, all subjects underwent a second MR and EEG data acquisition, as well as measurements of working memory capacity and cognition.

Connect with a study center

  • Fengdong New City Service Center for the Elderly

    Xi'an, Shaanxi 710086
    China

    Site Not Available

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