The Effects of Chicken Extract and a Peptide Supplement for the Prevention of Cognitive Decline in Non-demented Elderly Adults

  • STATUS
    Recruiting
  • End date
    Dec 1, 2023
  • participants needed
    276
  • sponsor
    Brand's Suntory Asia
Updated on 25 January 2022
Accepts healthy volunteers

Summary

This trial investigates the effect of a chicken extract supplement and a peptide supplement on cognitive function and potential mechanisms of action of cognitive decline during ageing, among non-demented elderly adults using a three-arm, randomized, placebo-controlled clinical trial design.

Details
Condition Cognitive Decline, Mild Cognitive Impairment, Aging
Treatment Placebo, Chicken extract supplement, Peptide Supplement
Clinical Study IdentifierNCT04555655
SponsorBrand's Suntory Asia
Last Modified on25 January 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Male or female at 55 - 75 years of age
Baseline cognition
Normal cognition with feelings of cognitive decline (subjective cognitive decline) OR
Mild cognitive impairment (MCI+) with memory impairment
Agree to participate in the study and provide written informed consent

Exclusion Criteria

Inadequate visual and auditory acuity to allow neuropsychological testing
Significant cerebrovascular disease
History of allergy to chicken meat
Diagnosis of Alzheimer's disease (AD) with dementia or any other dementia
Clinical dementia rating (CDR) score of > 0.5 at screening
Evidence of other neurological, psychiatric or physical illness that can produce cognitive deterioration per investigator's judgment
Inability or unwillingness to undergo PET scan
Current diagnosis or history of alcoholism or substance addiction
Regular use of any medication in the past 6 months that may affect cognitive functioning
Regular use of cognitive enhancing supplements in the past 6 months
Subjects with excessive blood donation or blood drawn prior to baseline
Persons with a history of cardiovascular disease or any other cardiovascular or cerebrovascular diseases which investigators deem unsuitable to participate in the clinical study
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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