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Non-pharmacological Intervention for Preclinical Alzheimer's Disease

Primary Purpose

Alzheimer Disease, Functional Food, Subjective Cognitive Decline

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Mixed functional foods supplementation
Placebo
Sponsored by
XuanwuH 2
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Alzheimer Disease focused on measuring Subjective cognitive decline, Mixed functional foods, Non-pharmacologic intervention

Eligibility Criteria

50 Years - 79 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 50-79 years old, right-handed and Mandarin-speaking subjects;
  • self-experienced persistent decline in cognitive capacity in comparison with a previously normal status and unrelated to an acute event;
  • normal age-adjusted, gender-adjusted and education-adjusted performance on standardised cognitive tests;
  • concerns (worries) associated with memory complaint;
  • failure to meet the criteria for MCI or dementia

Exclusion Criteria:

  • a history of stroke;
  • major depression (Hamilton Depression Rating Scale score > 24 points);
  • other central nervous system diseases that may cause cognitive impairment, such as Parkinson's disease, tumors, encephalitis and epilepsy;
  • cognitive impairment caused by traumatic brain injury;
  • systemic diseases, such as thyroid dysfunction, syphilis and HIV;
  • a history of psychosis or congenital mental growth retardation.

Sites / Locations

  • Department of Neurolgy, Xuanwu Hospital of Capital Medical University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Mixed functional foods group with SCD

Placebo group with SCD

Arm Description

Thirty participants in this group will take mixed functional foods for three months.

Thirty participants in this group will take placebo for three months.

Outcomes

Primary Outcome Measures

Changes of Auditory Verbal Learning Test (AVLT) score
After intervention for three months, the investigators will compare memory changes based on Auditory Verbal Learning Test (AVLT) scale in two groups, in order to investigate the therapeutic effectiveness of mixed functional foods supplementation. The scale of AVLT focuses on the memory domain, especially AVLT-long delayed memory, with cut-off points as 5 (50-59 years old), 4 (60-69 years old), 3 (70-79 years old) and AVLT-recognition, with cut-off points as 20 (50-59 years old), 19 (60-69 years old), 18 (70-79 years old). Higher scores mean a better outcome.

Secondary Outcome Measures

FNIRS-based brain functional activity changes
At baseline and post-intervention visits, the brain functional activity data will be collected using functional near-infrared spectroscopy (fNIRS) technique. The investigators will compare the changes of brain functional activity based on the measure of oxyhemoglobin concentration signal with relatively high signal to noise ratio (SNR) in two groups, in order to reveal the regulatory mechanism of mixed functional foods in intervening SCD persons.

Full Information

First Posted
February 16, 2020
Last Updated
February 19, 2020
Sponsor
XuanwuH 2
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1. Study Identification

Unique Protocol Identification Number
NCT04279418
Brief Title
Non-pharmacological Intervention for Preclinical Alzheimer's Disease
Official Title
Effects of Mixed Functional Foods Supplementation on Cognition and Neuroimaging Biomarkers in Adults With Subject Cognitive Decline
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Completed
Study Start Date
April 1, 2019 (Actual)
Primary Completion Date
August 31, 2019 (Actual)
Study Completion Date
December 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
XuanwuH 2

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Alzheimer's disease (AD) is the most common form of neurodegenerative disorders leading to dementia. Currently, there has been no effective drugs targeting this disease. Functional food is considered as a potentially non-pharmacologic treatment. In this project, the investigators aim to investigate the effectiveness of a mixed functional food with main compositions of ginsenoside, green tea polyphenols and marine collagen peptide on cognition for individuals with subjective cognitive decline (SCD). Taking the randomized, double-blind, placebo-controlled method, participants in the functional food group will take mixed functional foods for three months and those in the placebo group will take placebo. After that, the investigators will investigate the changes of cognitive function. Furthermore, based on the neuroimaging technique, the regulatory mechanism of functional food in intervening SCD will be revealed from the perspective of altered brain functional activity. In conclusion, these results are beneficial for understanding the therapeutic effect of mixed functional foods as a non-drug treatment for early AD and further elucidating the potential brain mechanism, which are of great values in solving scientific and clinical practice issues.
Detailed Description
Currently, there has been no effective therapy for Alzheimer's disease (AD). Functional food is now considered as a potentially non-pharmacologic intervention and supplementation of functional food may positively affect cognitive function for patients with AD. However, there are few existing studies involving the role of mixed functional foods with multiple compositions on cognition and neuroimaging biomarkers for subjective cognitive decline (SCD). Sixty participants with SCD will be recruited in this three-month, randomized, double-blind, placebo-controlled trial. Each group had thirty participants. Participants in the functional food group will take mixed functional foods for three months and those in the placebo group will take placebo. After that, the investigators will investigate the changes of memory measures, which is the primary outcome. Furthermore, based on the neuroimaging technique of functional near-infrared spectroscopy (fNIRS), the regulatory mechanism of mixed functional foods in intervening SCD will be revealed from the perspective of altered brain functional activity. In conclusion, these results are beneficial for understanding the therapeutic effect of mixed functional foods as a non-drug therapy for preclinical AD and further elucidating the potential brain mechanism, which are of great values in solving scientific and clinical practice issues.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer Disease, Functional Food, Subjective Cognitive Decline, Intervention, Neuroimaging
Keywords
Subjective cognitive decline, Mixed functional foods, Non-pharmacologic intervention

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mixed functional foods group with SCD
Arm Type
Experimental
Arm Description
Thirty participants in this group will take mixed functional foods for three months.
Arm Title
Placebo group with SCD
Arm Type
Placebo Comparator
Arm Description
Thirty participants in this group will take placebo for three months.
Intervention Type
Dietary Supplement
Intervention Name(s)
Mixed functional foods supplementation
Intervention Description
In this project, taking the method of random, double blindness and control, participants in the mixed functional foods group will take functional foods with main compositions of ginsenoside, green tea polyphenols and marine collagen peptide for three months. After that, neuropsychological tests and neuroimaging biomarkers will be compared between functional food group and placebo group.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
In this project, taking the method of random, double blindness and control, participants in the placebo group will take placebo for three months. After that, cognitive changes and neuroimaging biomarkers will be compared between functional food group and placebo group.
Primary Outcome Measure Information:
Title
Changes of Auditory Verbal Learning Test (AVLT) score
Description
After intervention for three months, the investigators will compare memory changes based on Auditory Verbal Learning Test (AVLT) scale in two groups, in order to investigate the therapeutic effectiveness of mixed functional foods supplementation. The scale of AVLT focuses on the memory domain, especially AVLT-long delayed memory, with cut-off points as 5 (50-59 years old), 4 (60-69 years old), 3 (70-79 years old) and AVLT-recognition, with cut-off points as 20 (50-59 years old), 19 (60-69 years old), 18 (70-79 years old). Higher scores mean a better outcome.
Time Frame
Three months
Secondary Outcome Measure Information:
Title
FNIRS-based brain functional activity changes
Description
At baseline and post-intervention visits, the brain functional activity data will be collected using functional near-infrared spectroscopy (fNIRS) technique. The investigators will compare the changes of brain functional activity based on the measure of oxyhemoglobin concentration signal with relatively high signal to noise ratio (SNR) in two groups, in order to reveal the regulatory mechanism of mixed functional foods in intervening SCD persons.
Time Frame
Three months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 50-79 years old, right-handed and Mandarin-speaking subjects; self-experienced persistent decline in cognitive capacity in comparison with a previously normal status and unrelated to an acute event; normal age-adjusted, gender-adjusted and education-adjusted performance on standardised cognitive tests; concerns (worries) associated with memory complaint; failure to meet the criteria for MCI or dementia Exclusion Criteria: a history of stroke; major depression (Hamilton Depression Rating Scale score > 24 points); other central nervous system diseases that may cause cognitive impairment, such as Parkinson's disease, tumors, encephalitis and epilepsy; cognitive impairment caused by traumatic brain injury; systemic diseases, such as thyroid dysfunction, syphilis and HIV; a history of psychosis or congenital mental growth retardation.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ying Han, PhD
Organizational Affiliation
Xuanwu Hospital of Capital Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Neurolgy, Xuanwu Hospital of Capital Medical University
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100053
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The information of neuropsychological tests, neuroimaging data are to be shared with other researchers.
IPD Sharing Time Frame
When summary data are published or starting 6 months after publication.
IPD Sharing Access Criteria
The information of neuropsychological tests, neuroimaging data will be shared.

Learn more about this trial

Non-pharmacological Intervention for Preclinical Alzheimer's Disease

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