- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06951932
Evaluation of the Impact of Medium-chain Fatty Acids in the Evolution of Newly Diagnosed Mild Cognitive Impairment (MCI-MCT)
April 30, 2025 updated by: Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo di Alessandria
Evaluation of the Impact of Medium-chain Fatty Acids in the Evolution of Newly Diagnosed Mild Cognitive Impairment: Prospective Randomized Controlled Trial
Mild cognitive impairment (MCI) is considered the intermediate stage between the changes observed in physiological aging and dementia.
Currently, there is no drug therapy, and available drugs offer only minimal benefit on symptoms, only partially slowing the course of the condition.
Studies in the literature have investigated the role of omega-3 fatty acids in MCI, and when administered over a period of six months, they appear to improve clinical condition and mood.
In addition, medium-chain triglycerides (MCTs) appear to exert an antioxidant function, enhance cognitive ability in patients with MCI or Alzheimer's, and promote deep sleep state.
Study Overview
Status
Recruiting
Conditions
Detailed Description
Mild cognitive impairment (MCI) is considered the intermediate stage between the changes observed in physiological aging and dementia.
The need to diagnose MCI at an early stage is driven by the hypothesis that therapeutic interventions may be more effective in the early stages of the disease.
In addition, many studies have shown that sleep disturbances can affect neurodegeneration and be used as a marker of disease, manifesting before cognitive impairment itself.
Currently, there is no drug therapy, and available drugs offer only minimal benefit on symptoms, only partially slowing the course of the condition.
Studies in the literature have investigated the role of omega-3 fatty acids in MCI, and when administered over a period of six months, they appear to improve clinical condition and mood.
In addition, medium-chain triglycerides (MCTs) appear to exert an antioxidant function, enhance cognitive ability in patients with MCI or Alzheimer's, and promote deep sleep state
Study Type
Interventional
Enrollment (Estimated)
120
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Prof. Luigi Mario Castello
- Phone Number: 0131206893
- Email: luigi.castello@ospedale.al.it
Study Locations
-
-
Piedmont
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Alessandria, Piedmont, Italy, 15121
- Recruiting
- Clinical Trial Center
-
Contact:
- Clinical Trial Center
- Phone Number: 0131206893
- Email: clinicaltrialcenter@ospedale.al.it
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Age between 18 and 85 years;
- Diagnosis of MCI;
- Disease duration of less than 24 months from symptom onset;
- Absence of malnutrition (diagnosed according to the NRS 2002 screening test) and with oral intakes sufficient to cover energy requirements (calculated by the Harris-Benedict formula, adjusted for activity factor and pathology);
- Ability to understand and sign informed consent.
Exclusion Criteria:
- Patients on total or supplemental enteral nutrition
- Severe dysphagia
- Patients with glycated hemoglobin > 8%
- Patients on insulin therapy
- Patients with poor beta-cell function (e.g., pancreasectomy, acute and chronic pancreatitis)
- Patients with liver failure: MELD score > 9
- Malnutrition (diagnosed according to the NRS 2002 screening test) and with per os intakes < 60% of energy requirements (calculated using the Harris-Benedict formula, corrected for activity factor and pathology)
- Metabolic disorders and/or enzyme disorders, dyslipidemia with total cholesterolemia >300 mg/dl and/or triglyceridemia >400 mg/dl)
- Acute inflammatory disease or ongoing or recent (within 30 days) infectious states
- Hypo- and hyperthyroidism not adequately compensated by treatment
- Heart failure (NYHA III-IV), unstable angina, recent (<6 months) acute cardiovascular or cerebrovascular events
- Pregnancy or lactation
- Neurological disorders other than MCI, psychiatric disorders
- Nutrition and eating disorder
- Alcohol abuse
- Institutionalized patients
- Participation in experimental therapies in the 2 months prior to enrollment
- Allergy to MCT oil, nuts
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Mediterranean-type food regimen using extra virgin olive oil
Patients with with first diagnosis of MCI referred to the S.C of Neurology and/or Geriatrics and/or Internal Medicine of the SS.
Antonio e Biagio e Cesare Arrigo of Alessandria University Hospital, randomized into the control arm
|
The arm will follow a Mediterranean diet with an indication to take extra virgin olive oil as the main fat in the diet daily
|
|
Experimental: Mediterranean-type diet with MCT supplementation
Patients with with first diagnosis of MCI referred to the S.C of Neurology and/or Geriatrics and/or Internal Medicine of the SS.
Antonio e Biagio e Cesare Arrigo of Alessandria University Hospital, randomized into the experimental arm
|
The treatment arm will follow a Mediterranean diet supplemented by daily intake of MCT (30 mL)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Effect of medium-chain triglycerides (MCT) intake on cognitive impairment
Time Frame: 6 months after baseline
|
Evaluate the effect of medium-chain triglycerides (MCT) intake on cognitive decline in patients with first diagnosis of MCI through the use of the Montreal Cognitive Assessment (MoCA), that includes a series of tests of visuospatial/executive functions, naming, attention, language, abstraction, delayed recall, and orientation for a total score of 30 (best cognitive status).
|
6 months after baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Positive effect of MCT intake on sleep quality
Time Frame: Baseline and 6 months after baseline
|
Evaluate the positive effect of MCT intake on sleep quality in patients with MCI using the Pittsburgh and Epworth Scales, sleep quality rating scales.
|
Baseline and 6 months after baseline
|
|
Evaluation of quality of life
Time Frame: Baseline, 3 months after baseline and 6 months after baseline
|
Assessing quality of life through the QoL AD score (Quality of life in Alzheimer's Disease), characterized by 15 items that can be answered by choosing from four options that are scored from 1 (poor) to 4 (excellent).
The total score ranges from 13 (worst quality of life) to 52 (best quality of life).
|
Baseline, 3 months after baseline and 6 months after baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 3, 2024
Primary Completion (Estimated)
July 3, 2025
Study Completion (Estimated)
November 3, 2025
Study Registration Dates
First Submitted
April 23, 2025
First Submitted That Met QC Criteria
April 23, 2025
First Posted (Actual)
April 30, 2025
Study Record Updates
Last Update Posted (Actual)
May 4, 2025
Last Update Submitted That Met QC Criteria
April 30, 2025
Last Verified
April 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ASO.MedI.23.02
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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