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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04990362
Other study ID # 69/5-6-2021
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 1, 2021
Est. completion date December 31, 2023

Study information

Verified date December 2022
Source Aristotle University Of Thessaloniki
Contact Magda Tsolaki, MD PhD Prof.
Phone 0030 2310 2411 56
Email tsolakim1@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 31, 2023
Est. primary completion date June 30, 2023
Accepts healthy volunteers No
Gender All
Age group 60 Years to 85 Years
Eligibility Inclusion Criteria: - Diagnosis of Mild Cognitive Impairment - Carry APOE e3 or e4 genes Exclusion Criteria: - Diagnosis of Dementia - Patients who receive medication for memory or depression - Patients who do not carry APOE e3 or e4 genes

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Pomegranate oil, Mediterranean Diet
Dietary Supplement: Pomegranate oil in a glass bottle of 0.15ml per day +Mediterranean dietary protocol Dietary Supplement: Mediterranean dietary protocol
Mediterranean Diet
Dietary Supplement: Mediterranean dietary protocol

Locations

Country Name City State
Greece Alzheimer Hellas Thessaloníki Thessaloniki

Sponsors (2)

Lead Sponsor Collaborator
Aristotle University Of Thessaloniki Greek Alzheimer's Association and Related Disorders

Country where clinical trial is conducted

Greece, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mini-Mental State Examination (MMSE Score scale:0-30,cut off:24 baseline,12 months
Primary FUCAS Measurements to Assess Daily Functionality Changes in Functional cognitive assessment scale (FUCAS) score Score scale:42-126,cut off:42 baseline,12 months
Primary Letter & Category Fluency Test Measurement to Assess Verbal Fluency and Learning Changes in the Letter & Category Fluency Test baseline,12 months
Primary CDR Measurements to Assess General Cognitive Function Changes in Global Clinical Dementia Rating (CDR) baseline,12 months
Primary MoCA Measurements to Assess General Cognitive Function Changes in Montreal Cognitive Assessment (MoCA) baseline,12 months
Primary CANTAB Measurements to Assess General Cognitive Function Changes in Cambridge Neuropsychological Test Automated Battery (CANTAB) baseline,12 months
Primary Clock Drawing test Measurements to Assess General Cognitive Function Changes in the Clock Drawing test baseline,12 months
Primary Logical Memory test Measurements to Assess General Cognitive Function Changes in the Logical Memory test baseline,12 months
Primary Digit Span Forward & Backward test Measurements to Assess General Cognitive Function Changes in the Digit Span Forward & Backward test baseline,12 months
Primary WAIS-R Digit Symbol Measurements to Assess General Cognitive Function Changes in the WAIS-R Digit Symbol Substitution Test baseline,12 months
Primary TMT part A and B Measurements to Assess General Cognitive Function Changes in the Trail Making Test baseline,12 months
Primary ADASCog Measurements to Assess Daily Functionality Changes in Alzheimer's Disease Assessment Scale-Cognitive (ADASCog) baseline,12 months
Primary Functional Rating Scale for Dementia Measurements to Assess Daily Functionality Changes in Functional Rating Scale for Dementia (FRSSD) baseline,12 months
Primary Auditory Verbal Learning Test Measurement to Assess Verbal Fluency and Learning Changes in the Auditory Verbal Learning Test baseline,12 months
Primary Boston Naming Test Measurement to Assess Verbal Fluency and Learning Changes in the Boston Naming Test baseline,12 months
Primary Fullerton Functional Test Measurement to Assess Physical Abilities baseline,12 months
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