PICFITE: Phosphatidylserine Improves Cognitive Function in the Elderly

Sponsor
First Affiliated Hospital Xi'an Jiaotong University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04920305
Collaborator
Air Force Military Medical University, China (Other), Fengdong New Town Elderlywelfare Service Center (Other)
100
1
2
16
6.3

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Phosphatidylserine
  • Dietary Supplement: Bean powder
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Clinical Study on the Effect of Phosphatidylserine on Cognitive Function Improvement in the Elderly
Anticipated Study Start Date :
Sep 1, 2022
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Phosphatidylserine group

subjects in the treatment group oral the PS (600mg/d, q.d.) for 6 months.

Dietary Supplement: Phosphatidylserine
subjects in the treatment group oral the PS (600mg/d, q.d.) for 6 months.

Placebo Comparator: Bean powder group

Subjects in the control group were given a placebo, which was the same shape of bean powder(600mg/d, q.d.) for 6 months.

Dietary Supplement: Bean powder
Subjects in the control group were given a placebo, which was the same shape of bean powder(600mg/d, q.d.).

Outcome Measures

Primary Outcome Measures

  1. The change of functional connectivity, points . [1 Year]

    the strength of functional connectivity, from 0 to 1

Secondary Outcome Measures

  1. The change of point in Montreal Cognitive Assessment (MoCA) test [1 Year]

    MOCA scale from 0 to 30, higher score means higher cognitive ability

  2. The change of point in Mini-mental State Examination (MMSE) test, points. [1 Year]

    MMSE scale from 0 to 30, higher score means higher cognitive ability

  3. The change of working memory test, points. [1Year.]

    The computer program to test memory ability, scale from 0 to 100, higher score means higher memory ability

Eligibility Criteria

Criteria

Ages Eligible for Study:
60 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Age 60 to 70, gender is not limited.
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 (more than 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, uncontrolled diabetes, endocrine, metabolic, blood disease, malignant disease, more than 2 years have not been relieved.

  • Taken any medication that may cause psychosis or affect intelligence in the past 1 month.

  • known allergy to phosphatidylserine or related ingredients.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Fengdong New City Service Center for the Elderly Xi'an Shaanxi China 710086

Sponsors and Collaborators

  • First Affiliated Hospital Xi'an Jiaotong University
  • Air Force Military Medical University, China
  • Fengdong New Town Elderlywelfare Service Center

Investigators

  • Study Director: Weimin Li, Dr., The First Affiliated Hospital of Xi 'an Jiaotong University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
First Affiliated Hospital Xi'an Jiaotong University
ClinicalTrials.gov Identifier:
NCT04920305
Other Study ID Numbers:
  • XJTU1AF2021LSY-200
First Posted:
Jun 9, 2021
Last Update Posted:
May 11, 2022
Last Verified:
May 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by First Affiliated Hospital Xi'an Jiaotong University

Study Results

No Results Posted as of May 11, 2022