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Effects of Hericium Erinaceus on Microbiota and Cognition (HE)

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ClinicalTrials.gov Identifier: NCT04939961
Recruitment Status : Completed
First Posted : June 25, 2021
Last Update Posted : March 1, 2023
Sponsor:
Information provided by (Responsible Party):
Zala Jenko Praznikar, University of Primorska

Tracking Information
First Submitted Date  ICMJE June 10, 2021
First Posted Date  ICMJE June 25, 2021
Last Update Posted Date March 1, 2023
Actual Study Start Date  ICMJE June 18, 2021
Actual Primary Completion Date September 20, 2021   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: June 17, 2021)
Assessment of the microbial community composition in feces samples using next-generation sequencing [ Time Frame: Change from Baseline Microbiota composition at 10 weeks. ]
For the assessment of the microbial community composition, DNA will be extracted from the frozen faecal samples (1-2 gram) with the commercial DNA Stool Mini Kit. A comparison of microbiota among treatments will be done with a meta-barcoding approach using ribosomal RNA markers with modified primers.
Original Primary Outcome Measures  ICMJE Same as current
Change History
Current Secondary Outcome Measures  ICMJE
 (submitted: June 17, 2021)
  • cognitive function [ Time Frame: Change from baseline Cognitive function at 10 weeks. ]
    Test of perception speed patterns, Test of series
  • brain derived neurotrophic factor [ Time Frame: Change from baseline Brain derived neurotrophic factor levels at 10 weeks. ]
    serum level measured with ELISA assay
  • neuropeptide Y [ Time Frame: Change from baseline Neuropeptide Y levels at 10 weeks. ]
    serum level measured with ELISA assay
Original Secondary Outcome Measures  ICMJE Same as current
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Effects of Hericium Erinaceus on Microbiota and Cognition
Official Title  ICMJE Effects of Hericium Erinaceus on Microbiota and Cognition in Older Adults
Brief Summary The study evaluates the effects of Hericium erinaceus on microbiota, cognition, and other health parameters in older adults. All measurements will be performed at baseline and ten weeks after daily consumptions of either Hericium erinaceus or placebo.
Detailed Description

Hericium erinaceus, a well-known edible mushroom, has numerous biological activities. Yamabushitake (Hericium erinaceus) is a mushroom that grows on both living and dead broadleaf trees. Yamabushitake is used as food in Japan and China. Hericenones and erinacines stimulate nerve growth factor synthesis, and therefore it is expected that H. erinaceus have some effects on brain functions and autonomic nervous system. Hericium was tested in several applications, such as dementia, Alzheimer's disease, Parkinson's disease, multiple sclerosis, neuropathy and neurasthenia. The ancient Chinese knew about these possibilities and used it to support mental functions and memory, concentration. It is also very good for various digestive problems, such as gastritis, stomach ulcers, heartburn, reflux and improvement of digestion.

Therefore, the aim of our study is to evaluate the effects of Hericium erinaceus on microbiota, cognition and related parameters in elderly. The stool samples will be taken at baseline and after ten weeks of daily consumption of Hericium erinaceus or placebo. In addition, cognitive tests, anthropometric measurements, and blood analysis (lipid profile, glucose levels and neurotrophic factors) will be measured at the same time points.

Study Type  ICMJE Interventional
Study Phase  ICMJE Not Applicable
Study Design  ICMJE Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description:
Randomized placebo controlled
Masking: Double (Participant, Investigator)
Masking Description:
Placebo and experimental capsules (A and B) were prepared by collaborator-investigator (MycoMedica). Both experimental and placebo capsules appear similar to each other in terms of colour, flavour, size, and shape to make sure that they cannot be distinguished. Information about capsules will be provided to participants and investigators at the end of the trial.
Primary Purpose: Prevention
Condition  ICMJE Cognitive Decline, Mild
Intervention  ICMJE
  • Dietary Supplement: Hericium erinaceus
    6 capsules per day, 3 times two after breakfast, lunch and dinner
  • Dietary Supplement: Placebo
    6 capsules per day, 3 times two after breakfast, lunch and dinner
Study Arms  ICMJE
  • Experimental: Hericium erinaceus
    8 gram of mushroom Hericium erinaceus (containing 5 milligram of erinacines) per day
    Intervention: Dietary Supplement: Hericium erinaceus
  • Placebo Comparator: Placebo capsule
    8 gram of allergen free corn starch per day
    Intervention: Dietary Supplement: Placebo
Publications *

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Completed
Actual Enrollment  ICMJE
 (submitted: June 17, 2021)
40
Original Estimated Enrollment  ICMJE Same as current
Actual Study Completion Date  ICMJE December 20, 2022
Actual Primary Completion Date September 20, 2021   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  • age 55 - 75 years

Exclusion Criteria:

  • neurodegenerative disease
  • organ transplantation
  • allergy to fungi
  • antibiotic consumption in the previous 3 months
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 55 Years to 75 Years   (Adult, Older Adult)
Accepts Healthy Volunteers  ICMJE Yes
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE Slovenia
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT04939961
Other Study ID Numbers  ICMJE Hericium erinaceus
Has Data Monitoring Committee No
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement  ICMJE
Plan to Share IPD: No
Current Responsible Party Zala Jenko Praznikar, University of Primorska
Original Responsible Party Same as current
Current Study Sponsor  ICMJE University of Primorska
Original Study Sponsor  ICMJE Same as current
Collaborators  ICMJE Not Provided
Investigators  ICMJE Not Provided
PRS Account University of Primorska
Verification Date February 2023

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP