Influence of Oxidative Stress and Nutrition Biomarkers on the Cognitive Decline Evolution in Alzheimer Disease

NCT ID: NCT02800395

Last Updated: 2021-04-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

350 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-12-31

Study Completion Date

2026-12-31

Brief Summary

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According to several reports, the oxidative stress and the nutrition could have an impact in the Alzheimer disease.

The association of these two parameters measurements and the cognitive impairment decline could help in a predictive diagnosis of cognitive decline evolution in patients presenting cognitive disorders.

This is a monocentric prospective "routine care" clinical trial on patients showing cognitive troubles especially memory complaints.

The objective is to demonstrate a correlation between oxydative stress and nutrition biomarkers and the clinical evolution of patients complaining of cognitive impairments.

The neuropsychologic data collection (the mini mental Status Examination (MMSE), the clock test, the Grober-Buschke test (FCSR-IR), the executive function evaluated by the Trail making test, and the medical imaging (by magnetic resonance imaging (MRI) or tomography in case of MRI contraindication) will be realized during the study inclusion phase in the usual intake of patients. Whole blood samples for the oxydative and nutrition biomarkers measurements will be taken at the study inclusion day during the stay at the Day hospital dedicated to the routine intake of patients issued from the memory consultation.

In this study, the principal evaluation criteria will be the MMSE score evolution during the 60 months of the patients follow-up, measured during the routine visits scheduled approximately every 6 months, according to the french national authority for health recommendations. It will allow evaluating the correlation between the cognitive decline evolution measured by MMSE during the Alzheimer disease or related diseases method during the 2 years follow-up, and the oxydative stress blood markers.

Detailed Description

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Conditions

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Alzheimer Disease

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Nutritional evaluation

Group Type OTHER

Malnutrition screening and perioperative nutritional support

Intervention Type PROCEDURE

* Multidisciplinary training sessions for malnutrition and malnutrition risk screening, postoperative nutritional procedures according to the ESPEN Guidelines
* Preoperative Geriatric evaluation : eligibility criteria, nutritional status, previous history, comorbidities, clinical examination, activities of daily living (ADL) and Instrumental activities of daily living (IADL)
* Implementation of an adapted nutritional support based on ESPEN Guidelines

Interventions

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Malnutrition screening and perioperative nutritional support

* Multidisciplinary training sessions for malnutrition and malnutrition risk screening, postoperative nutritional procedures according to the ESPEN Guidelines
* Preoperative Geriatric evaluation : eligibility criteria, nutritional status, previous history, comorbidities, clinical examination, activities of daily living (ADL) and Instrumental activities of daily living (IADL)
* Implementation of an adapted nutritional support based on ESPEN Guidelines

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* \>55 years old patient
* Patient seen during a memory consultation in geriatric Unit, Lyon Sud University Hospital
* Patient or legal representative and/or person of confidence who didn't express his opposition to the clinical assay participation.
* Patient registered to the general social insurance
* Complementary health check scheduled at day hospital, conventional hospitalization or regular consultation.

Exclusion Criteria

* Patient unable to express his participation refusal and under curatorship or unforced by the court of justice
Minimum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hospices Civils de Lyon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Marc BONNEFOY, Pr

Role: PRINCIPAL_INVESTIGATOR

Hospices Civils de Lyon

Locations

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Service de Médecine Gériatrique. Groupement Hospitalier Sud. Hospices Civils de Lyon.

Pierre-Bénite, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Marc BONNEFOY, Pr

Role: CONTACT

(0)4 78 86 15 81 ext. +33

Facility Contacts

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Marc BONNEFOY, Pr

Role: primary

(0)4 78 86 15 81 ext. +33

Other Identifiers

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2014.860

Identifier Type: -

Identifier Source: org_study_id

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