Effect of Nutritional Supplementation With Turmeric on the Cognitive Performance of Subjects With Metabolic Syndrome (EPICURO)

January 29, 2026 updated by: Indena S.p.A
The EPICURO study aims to demonstrate the beneficial effects of a 6-month dietary supplementation with an improved bioavailable turmeric (MERIVA®) on inflammatory, oxidative and metabolic parameters together with cognitive performance, potentially resulting in the reduction of the risk of cognitive decline in subjects, male and female, with Metabolic Syndrome. The results obtained will provide novel insights on MERIVA® for improving the prevention of age-related cognitive decline and Alzheimer's disease.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This single-center trial will be a placebo-controlled, double-blind, randomized, 2 parallel groups study. The subjects will be randomly allocated to one of two treatment groups (MERIVA® or placebo). The duration of the supplementation is 6 months. The total sample size at baseline is 100 subjects aged 60+ years with Metabolic Syndrome, and therefore at risk of cognitive decline but without definite cognitive pathologies.

The primary objective of the study is the evaluation of the effect of nutritional supplementation with MERIVA® on the cognitive performance of subjects with Metabolic Syndrome, and therefore at risk of cognitive decline, with a view to maintaining the homeostatic balance of the function.

The secondary objectives of the study are:

  • Evaluation of the effect of nutritional supplementation with turmeric (MERIVA®) on memory, executive and attention functions, language, neuropsychiatric profile and daily living ability of Subjects with Metabolic Syndrome;
  • Evaluation of the effect of nutritional supplementation with turmeric (MERIVA®) on the body composition of Subjects with Metabolic Syndrome;
  • Evaluation of the effect of nutritional supplementation with turmeric (MERIVA®) on the arterial properties of Subjects with Metabolic Syndrome;
  • Evaluation of the effect of nutritional supplementation with turmeric (MERIVA®) on glucose metabolism and on the lipid and immune structure of Subjects with Metabolic Syndrome;
  • Evaluation of the influence of gender / gender on the response to nutritional supplementation with turmeric (MERIVA®) in Subjects with Metabolic Syndrome;
  • Confirmation of the safety profile of nutritional supplementation with turmeric (MERIVA®) in Subjects with Metabolic Syndrome.

Study Type

Interventional

Enrollment (Actual)

85

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 Locations

  • Italy
      • Roma, Italy, 00168
        • S.C. di Endocrinologia e Diabetologia, Policlinico Universitario "Agostino Gemelli"

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

60 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Male or female subjects.
  • Subjects aged ≥ 60 years.

  • Subjects with Metabolic Syndrome diagnosed according to standard criteria:

    1. Presence of abdominal obesity (waist circumference> 94 cm for males and> 80 cm for females).

      In addition, at least two of the following alterations:

    2. Fasting blood glucose ≥ 100 mg / dl.
    3. Triglycerides ≥ 150 mg / dl.
    4. HDL cholesterol <40 mg / dl for males, <50 mg / dl for females.
    5. Arterial hypertension (≥ 135/85 mmHg).
  • Subjects who understand the nature of the study and provide their informed consent to participate.
  • Subjects willing and able to participate in the visits and in the procedures foreseen by the study protocol.

Exclusion Criteria:

  • Subjects with dementia with MMSE <24 test and on therapy with cholinesterase inhibitors or memantine*.
  • Subjects with serious concomitant internal medical conditions or with neurological pathologies capable of causing cognitive dysfunction.
  • Subjects with hepato-biliary disorders, including bile duct obstruction, cholangitis, gallstones.
  • Subjects addicted to alcohol or drugs, or treated with psychotropic drugs at the time of enrollment.
  • Subjects with known or suspected allergy or hypersensitivity to turmeric or other components of the experimental / placebo product.
  • Subjects with Mild Cognitive Impairment (MCI) and in experimental therapy with Alzheimer's disease drugs.
  • Subjects who are participating or have participated in other clinical studies within 30 days before enrollment.

  • Subjects unable to sign the Informed Consent to Participation.

    • In case of conversion to dementia the Subjects will be kept in the study, will be subjected to the most appropriate therapies provided for the dementia pathology but will not enter the subsequent statistical evaluations.

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Nutritional Supplementation with Test Product
Subjects will receive 1 tablet of MERIVA® in two administrations per day (one in the morning, one in the evening during meals) for a period of 6 months. This treatment corresponds to 1 g / day of experimental product (corresponding to about 200 mg of curcuminoids).
Dietary supplement: MERIVA® Tablets
The treatment corresponds to 1 g / day of experimental product (corresponding to about 200 mg of curcuminoids).
Placebo Comparator: Control Group without Nutritional Supplementation
Subjects will receive 1 tablet of placebo in two administrations per day (one in the morning, one in the evening during meals) for a period of 6 months.
Other: Placebo Tablets
The composition of placebo includes the same components of the treatment tablets, except for the active substance.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from Baseline of Mini-Mental State Examination (MMSE) Test
Time Frame: Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).
Percentage of subjects showing an improvement in performance in Mini-Mental State Examination (MMSE) test in comparison to baseline, defined as an increase of more than 2 points in the test. A difference between the group treated with MERIVA® versus placebo of at least 20% in the proportion of subjects with clinical improvement as defined above is considered clinically relevant. The differences between genders are considered.
Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).
Change from Baseline of Montreal Cognitive Assessment (MOCA) Test
Time Frame: Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).
Percentage of subjects showing an improvement in performance in Montreal Cognitive Assessment (MOCA) test in comparison to baseline, defined as an increase of more than 2 points in the test. A difference between the group treated with MERIVA® versus placebo of at least 20% in the proportion of subjects with clinical improvement as defined above is considered clinically relevant. The differences between genders are considered.
Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from Baseline of Rey's Auditory Verbal Learning Test (RAVLT) Test
Time Frame: Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).

Evaluation in comparison to baseline of the neuropsychological measurement performed regarding memory tests (Rey's Auditory Verbal Learning Test - RAVLT). Any differences between the groups treated with MERIVA® versus placebo will be recorded.

The differences between genders are considered.
Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).
Change from Baseline of Trail Making Test (TMT) Test
Time Frame: Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).

Evaluation in comparison to baseline of the neuropsychological measurement performed regarding executive functions and attention (Trail Making Test - TMT). Any differences between the groups treated with MERIVA® versus placebo will be recorded.

The differences between genders are considered.
Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).
Change from Baseline of Multiple Features Target Cancellation (MFTC) Test
Time Frame: Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).

Evaluation in comparison to baseline of the neuropsychological measurement performed regarding executive functions and attention (Multiple Features Target Cancellation - MFTC). Any differences between the groups treated with MERIVA® versus placebo will be recorded.

The differences between genders are considered.
Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).
Change from Baseline of Phonological and Semantic Verbal Fluidity (FVS) Test
Time Frame: Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).

Evaluation in comparison to baseline of the neuropsychological measurement performed regarding language (Phonological and Semantic Verbal Fluidity - FVS). Any differences between the groups treated with MERIVA® versus placebo will be recorded.

The differences between genders are considered.
Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).
Change from Baseline of Geriatric Depression Scale (GDS) Test
Time Frame: Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).

Evaluation in comparison to baseline of the neuropsychological measurement performed regarding a neuropsychiatric scale (Geriatric Depression Scale - GDS). Any differences between the groups treated with MERIVA® versus placebo will be recorded.

The differences between genders are considered.
Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).
Change from Baseline of Neuro-Psychiatric Inventory (NPI) Test
Time Frame: Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).

Evaluation in comparison to baseline of the neuropsychological measurement performed regarding a neuropsychiatric scale (Neuro-Psychiatric Inventory - NPI). Any differences between the groups treated with MERIVA® versus placebo will be recorded.

The differences between genders are considered.
Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).
Change from Baseline of Basic Activities of Daily Living (BADL) Test
Time Frame: Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).

Evaluation in comparison to baseline of the neuropsychological measurement performed regarding the ability to live everyday (Basic Activities of Daily Living - BADL). Any differences between the groups treated with MERIVA® versus placebo will be recorded.

The differences between genders are considered.
Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).
Change from Baseline of Instrumental Activities of Daily Living (IADL) Test
Time Frame: Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).

Evaluation in comparison to baseline of the neuropsychological measurement performed regarding the ability to live everyday (Instrumental Activities of Daily Living - IADL). Any differences between the groups treated with MERIVA® versus placebo will be recorded.

The differences between genders are considered.
Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).
Change from Baseline of Stroop Test - Short Version
Time Frame: Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).

Evaluation in comparison to baseline of the neuropsychological measurement performed regarding executive functions and attention (Stroop test short version). Any differences between the groups treated with MERIVA® versus placebo will be recorded.

The differences between genders are considered.
Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).
Change from Baseline of Bioelectrical Impedance (BIA) Assessment
Time Frame: Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).

Evaluation in comparison to baseline of body composition by bioelectrical impedance (BIA). Any differences between the groups treated with MERIVA® versus placebo will be recorded.

The differences between genders are considered.
Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).
Change from Baseline of Metabolism Parameters measured in Blood
Time Frame: Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).

Evaluation in comparison to baseline of metabolism changes (blood panel including: total cholesterol, Low-Density Lipoproteins, High-Density Lipoproteins, insulin, triglycerides, glucose, creatinine, uric acid, electrolytes, hepatic transaminases, gamma-glutamyltransferase, total proteins). In particular, any differences in terms of fasting blood glucose reduction and Homeostatic Model Assessment (HOMA) Index between the groups treated with MERIVA® versus placebo will be recorded.

The differences between genders are considered.
Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).
Change from Baseline of Lipid and Immune Profile measured in Blood
Time Frame: Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).

Evaluation in comparison to baseline of the lipid and immune profile of subjects treated with MERIVA® versus placebo. In particular, an omic-type approach will reveal alterations in lipid and energy metabolism, including lipoproteins, low molecular weight metabolites and individual lipid molecules, together with their degree of (poly) (non) saturation (blood panel including: leptin, adiponectin, Brain-derived Neurotrophic Factor, proinflammatory mediators such as Tumor Necrosis Factor alpha, interleukin-1 beta and interleukin-6, prostaglandins and reactive species of oxygen / nitrogen, inflammasome).

The differences between genders are considered.
Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).
Change from Baseline of Brain-Derived Neurotrophic Factor (BDNF) and p66Shc Gene Expression measured in Blood
Time Frame: Change from Baseline (T0) to 6 months of treatment (T6).

Evaluation in comparison to baseline of the lipid and immune profile of subjects treated with MERIVA® versus placebo. In particular, a sample of Peripheral Blood Mononuclear Cells (PBMC) will be separated for the measurement of the expression, by means of real-time Polymerase Chain Reaction (RT-PCR), of the neurotrophin Brain-Derived Neurotrophic Factor (BDNF) and of the p66Shc gene, which are involved in the response to lifestyle changes, including diets and exercise.

The differences between genders are considered.
Change from Baseline (T0) to 6 months of treatment (T6).
Rate and Characterization of Adverse Events occurred to Subjects
Time Frame: Pre-Screening (T-1) / Baseline (T0) / After 3 months of treatment (T3) / After 6 months of treatment (T6) / After 12 months of treatment (T12).

Evaluation of the number, rate and characteristics of the adverse events occurring to subjects treated with MERIVA® versus placebo.

The differences between genders are considered.
Pre-Screening (T-1) / Baseline (T0) / After 3 months of treatment (T3) / After 6 months of treatment (T6) / After 12 months of treatment (T12).

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Intestinal Microbiotic Profile Assessment in Stool Sample
Time Frame: Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).

Evaluation in comparison to baseline of the intestinal microbiotic profile of subjects. Any differences between the groups treated with MERIVA® versus placebo will be recorded.

The differences between genders are considered.
Change from Baseline (T0) to 6 months of treatment (T6) and 12 months of treatment (T12).

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Indena S.p.A

Collaborators

Istituto Superiore di Sanità
Sintesi Research Srl

Investigators

  • Principal Investigator: Andrea Giaccari, Prof., Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

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)

April 8, 2022

Primary Completion (Actual)

October 16, 2025

Study Completion (Actual)

December 19, 2025

Study Registration Dates

First Submitted

December 6, 2019

First Submitted That Met QC Criteria

January 11, 2021

First Posted (Actual)

January 12, 2021

Study Record Updates

Last Update Posted (Actual)

February 2, 2026

Last Update Submitted That Met QC Criteria

January 29, 2026

Last Verified

December 1, 2025

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CUR-01-2019

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

product manufactured in and exported from the U.S.

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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