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Effects of Pomegranate Seed Oil and Mediterranean Diet on MCI

Primary Purpose

Mild Cognitive Impairment

Status
Recruiting
Phase
Not Applicable
Locations
Greece
Study Type
Interventional
Intervention
Pomegranate oil, Mediterranean Diet
Mediterranean Diet
Sponsored by
Aristotle University Of Thessaloniki
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mild Cognitive Impairment focused on measuring Mild Cognitive Impairment, Cognition, Mental Health, APOE, ε3/ε3, ε3/ε2, ε3/ε4, ε2/ε4, ε4/ε4, Pomegranate oil

Eligibility Criteria

60 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of Mild Cognitive Impairment
  • Carry APOE ε3 or ε4 genes

Exclusion Criteria:

  • Diagnosis of Dementia
  • Patients who receive medication for memory or depression
  • Patients who do not carry APOE ε3 or ε4 genes

Sites / Locations

  • Alzheimer HellasRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

MD + Seed oil

MD

Arm Description

Pomegranate oil + Mediterranean Diet 30 patients Mediterranean dietary protocol Dietary Supplement: Pomegranate oil in a glass bottle of 30ml Dietary Supplement: Mediterranean dietary protocol Intervention: Mediterranean diet, Pomegranate oil

Mediterranean Diet 30 patients Mediterranean dietary protocol Dietary Supplement: Mediterranean dietary protocol Intervention: Mediterranean diet

Outcomes

Primary Outcome Measures

Mini-Mental State Examination (MMSE
Score scale:0-30,cut off:24
FUCAS
Measurements to Assess Daily Functionality Changes in Functional cognitive assessment scale (FUCAS) score Score scale:42-126,cut off:42
Letter & Category Fluency Test
Measurement to Assess Verbal Fluency and Learning Changes in the Letter & Category Fluency Test
CDR
Measurements to Assess General Cognitive Function Changes in Global Clinical Dementia Rating (CDR)
MoCA
Measurements to Assess General Cognitive Function Changes in Montreal Cognitive Assessment (MoCA)
CANTAB
Measurements to Assess General Cognitive Function Changes in Cambridge Neuropsychological Test Automated Battery (CANTAB)
Clock Drawing test
Measurements to Assess General Cognitive Function Changes in the Clock Drawing test
Logical Memory test
Measurements to Assess General Cognitive Function Changes in the Logical Memory test
Digit Span Forward & Backward test
Measurements to Assess General Cognitive Function Changes in the Digit Span Forward & Backward test
WAIS-R Digit Symbol
Measurements to Assess General Cognitive Function Changes in the WAIS-R Digit Symbol Substitution Test
TMT part A and B
Measurements to Assess General Cognitive Function Changes in the Trail Making Test
ADASCog
Measurements to Assess Daily Functionality Changes in Alzheimer's Disease Assessment Scale-Cognitive (ADASCog)
Functional Rating Scale for Dementia
Measurements to Assess Daily Functionality Changes in Functional Rating Scale for Dementia (FRSSD)
Auditory Verbal Learning Test
Measurement to Assess Verbal Fluency and Learning Changes in the Auditory Verbal Learning Test
Boston Naming Test
Measurement to Assess Verbal Fluency and Learning Changes in the Boston Naming Test
Fullerton Functional Test
Measurement to Assess Physical Abilities

Secondary Outcome Measures

Full Information

First Posted
July 26, 2021
Last Updated
December 12, 2022
Sponsor
Aristotle University Of Thessaloniki
Collaborators
Greek Alzheimer's Association and Related Disorders
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1. Study Identification

Unique Protocol Identification Number
NCT04990362
Brief Title
Effects of Pomegranate Seed Oil and Mediterranean Diet on MCI
Official Title
Effects of Pomegranate Seed Oil and Mediterranean Diet at Motor Skills and Cognitive Abilities in Mild Cognitive Impairment.
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 1, 2021 (Actual)
Primary Completion Date
June 30, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aristotle University Of Thessaloniki
Collaborators
Greek Alzheimer's Association and Related Disorders

4. Oversight

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

5. Study Description

Brief Summary
A double-blind clinical trial of pomegranate oil and Mediterranean diet that will be carried out on 60 patients with Mild Cognitive Impairment (MCI) and APOE ε3 and ε4 allele. The aim of the research is to examine if the Mediterranean diet with pomegranate oil and without it can bring positive changes in patients with MCI in terms of motor and cognitive skills.
Detailed Description
OBJECTIVES OF THE TRIAL The objectives of this study are: To investigate the efficacy of Mediterranean diet and Pomegranate oil as a disease course modifying treatment for MCI. STUDY DESIGN This is a Greek, controlled double-blind trial of two compared groups, one with Mediterranean diet and one with Mediterranean diet and pomegranate oil. Qualifying patients will be assigned to receive 0.15 mL of pomegranate oil every day with Mediterranean diet at one group and at the other group will not. A Mediterranean dietary protocol will be given on a daily basis for 12 months at both groups. Duration The total study duration will be 12 months. The recruitment will be about 6 months and the statistics and the preparation of the paper other 6 months. Number of Subjects: Sixty (60) subjects total will be enrolled.; Thirty (30) in the A group (Pomegranate oil + Mediterranean Diet); Thirty (30) in the B Group (Mediterranean Diet). Patient identification: Initials (First initial of first name and First initial of surname), date of birth and Patient Identification Number from database empedocles. Eligibility Screening Form (ESF) : Checklist of inclusion and exclusion criteria Eligibility Statement: for patients found to be ineligible, the reason for ineligibility must be stated and Written informed consent will be obtained from the subjects which are eligible. The informed consent form must be co-signed by the physician. The nature of the study and the potential risks associated with the trial will be explained to all subjects- candidates and their responsible informants. Signature and date: the ESF may be completed by a research assistant but it is required that the principal investigator/study clinician sign and date the ESF to verify eligibility of the patient for inclusion.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mild Cognitive Impairment
Keywords
Mild Cognitive Impairment, Cognition, Mental Health, APOE, ε3/ε3, ε3/ε2, ε3/ε4, ε2/ε4, ε4/ε4, Pomegranate oil

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MD + Seed oil
Arm Type
Experimental
Arm Description
Pomegranate oil + Mediterranean Diet 30 patients Mediterranean dietary protocol Dietary Supplement: Pomegranate oil in a glass bottle of 30ml Dietary Supplement: Mediterranean dietary protocol Intervention: Mediterranean diet, Pomegranate oil
Arm Title
MD
Arm Type
Active Comparator
Arm Description
Mediterranean Diet 30 patients Mediterranean dietary protocol Dietary Supplement: Mediterranean dietary protocol Intervention: Mediterranean diet
Intervention Type
Dietary Supplement
Intervention Name(s)
Pomegranate oil, Mediterranean Diet
Intervention Description
Dietary Supplement: Pomegranate oil in a glass bottle of 0.15ml per day +Mediterranean dietary protocol Dietary Supplement: Mediterranean dietary protocol
Intervention Type
Dietary Supplement
Intervention Name(s)
Mediterranean Diet
Intervention Description
Dietary Supplement: Mediterranean dietary protocol
Primary Outcome Measure Information:
Title
Mini-Mental State Examination (MMSE
Description
Score scale:0-30,cut off:24
Time Frame
baseline,12 months
Title
FUCAS
Description
Measurements to Assess Daily Functionality Changes in Functional cognitive assessment scale (FUCAS) score Score scale:42-126,cut off:42
Time Frame
baseline,12 months
Title
Letter & Category Fluency Test
Description
Measurement to Assess Verbal Fluency and Learning Changes in the Letter & Category Fluency Test
Time Frame
baseline,12 months
Title
CDR
Description
Measurements to Assess General Cognitive Function Changes in Global Clinical Dementia Rating (CDR)
Time Frame
baseline,12 months
Title
MoCA
Description
Measurements to Assess General Cognitive Function Changes in Montreal Cognitive Assessment (MoCA)
Time Frame
baseline,12 months
Title
CANTAB
Description
Measurements to Assess General Cognitive Function Changes in Cambridge Neuropsychological Test Automated Battery (CANTAB)
Time Frame
baseline,12 months
Title
Clock Drawing test
Description
Measurements to Assess General Cognitive Function Changes in the Clock Drawing test
Time Frame
baseline,12 months
Title
Logical Memory test
Description
Measurements to Assess General Cognitive Function Changes in the Logical Memory test
Time Frame
baseline,12 months
Title
Digit Span Forward & Backward test
Description
Measurements to Assess General Cognitive Function Changes in the Digit Span Forward & Backward test
Time Frame
baseline,12 months
Title
WAIS-R Digit Symbol
Description
Measurements to Assess General Cognitive Function Changes in the WAIS-R Digit Symbol Substitution Test
Time Frame
baseline,12 months
Title
TMT part A and B
Description
Measurements to Assess General Cognitive Function Changes in the Trail Making Test
Time Frame
baseline,12 months
Title
ADASCog
Description
Measurements to Assess Daily Functionality Changes in Alzheimer's Disease Assessment Scale-Cognitive (ADASCog)
Time Frame
baseline,12 months
Title
Functional Rating Scale for Dementia
Description
Measurements to Assess Daily Functionality Changes in Functional Rating Scale for Dementia (FRSSD)
Time Frame
baseline,12 months
Title
Auditory Verbal Learning Test
Description
Measurement to Assess Verbal Fluency and Learning Changes in the Auditory Verbal Learning Test
Time Frame
baseline,12 months
Title
Boston Naming Test
Description
Measurement to Assess Verbal Fluency and Learning Changes in the Boston Naming Test
Time Frame
baseline,12 months
Title
Fullerton Functional Test
Description
Measurement to Assess Physical Abilities
Time Frame
baseline,12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of Mild Cognitive Impairment Carry APOE ε3 or ε4 genes Exclusion Criteria: Diagnosis of Dementia Patients who receive medication for memory or depression Patients who do not carry APOE ε3 or ε4 genes
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Magda Tsolaki, MD PhD Prof.
Phone
0030 2310 2411 56
Email
tsolakim1@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Thanos Chatzikostopoulos, MSc
Phone
0030 2310351451
Email
thachatziko@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Magda Tsolaki, MD PhD Prof.
Organizational Affiliation
Greek Alzheimer's Association and Related Disorders
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Thanos Chatzikostopoulos, MSc
Organizational Affiliation
Greek Alzheimer's Association and Related Disorders
Official's Role
Principal Investigator
Facility Information:
Facility Name
Alzheimer Hellas
City
Thessaloníki
State/Province
Thessaloniki
Country
Greece
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Participants' personal data will not be shared with other researchers

Learn more about this trial

Effects of Pomegranate Seed Oil and Mediterranean Diet on MCI

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