search
Back to results

Study to Evaluate the Effect of a Vegetal Oil on Cognitive Impairment

Primary Purpose

Cognitive Impairments, Alzheimer Disease

Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Lipidic Blend 1
Lipidic Blend 2
Placebo
Sponsored by
Team Foods Colombia S.A.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cognitive Impairments focused on measuring Cognitive Impairment, Alzheimer's Disease, Vegetal Oil

Eligibility Criteria

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

Inclusion Criteria:

  • informed consents signed by patients and/or caretaker
  • The patient has to fulfil dementia clinical criteria.
  • Age between 55 and 85 years old.
  • MMSE score between 18 and 26.
  • The patient can fulfil all neuropsychologic test, according to investigator.
  • The patient has to be always with his/her caretaker during monitorization visits
  • The caretaker has to be in regular contact with the patient, knowing his/her situation and participation in the study.
  • The caretaker has to check four times per week, at least, the product intake, as well as the routine medication and his/her dietetic habits.
  • Both caretaker and patient have to be able to complete the product intake during all the length of the study, according to the main investigator.

Exclusion Criteria:

  • Patient and/or caretaker not being able to understand and agree in writing their participation in the study.
  • Patient disability to oral intake of products.
  • Known allergy to any of the product components (active and placebo)
  • Evidence of suffering other neuropsychiatric disturbances apart of dementia as: Parkinson disease, psychotic disturbance, bipolar depression.
  • regular intake of alcohol higher than 45 g ethanol/day, during the year before study inclusion.
  • Any known concurrent malignant pathology in the moment of study inclusion, or severe metabolic, cardiovascular, renal, hepatic, or gastrointestinal disease that cannot allow the ending of the study according the investigator.
  • Any analytical abnormality during the screening, apart from: Creatinine no less than 1.7 mg/dL; low levels of Vitamin B12, and TSH abnormal values.

Sites / Locations

  • Hospital Universitario VinalopóRecruiting
  • Hospital Universitario de TorreviejaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

Lipidic Blend 1

Lipidic Blend 2

Placebo

Arm Description

Glass bottle with 45 ml of vegetal mixture oil. 1 bottle per day

Glass bottle with 45 ml of vegetal mixture oil. 1 bottle per day

Glass bottle with 45 ml of Olive oil. 1 bottle per day

Outcomes

Primary Outcome Measures

Changes in Mini-Mental State Examination (MMSE) score
Changes in Global Clinical Dementia Rating (CDR) score

Secondary Outcome Measures

Changes in systemic oxidative parameters in periferic blood samples (Nitric Oxyde)
Changes in systemic oxidative parameters in periferic blood samples (Malondialdehyde (MDA))
Changes in beta-amyloid protein concentration
Changes in mean values on high sensitivity beta-amyloid 1-40 and 1-42 protein and TAU-protein in cerebrospinal fluid on those patients with a new diagnose of mild to moderate cognitive impairment, that require an initial lumbar puncture and a new lumbar puncture to control evolution at the end of teh study.
Changes in TAU-Protein concentration
Changes in mean values on high sensitivity beta-amyloid 1-40 and 1-42 protein and TAU-protein in cerebrospinal fluid on those patients with a new diagnose of mild to moderate cognitive impairment, that require an initial lumbar puncture and a new lumbar puncture to control evolution at the end of teh study.
Changes in regular treatment for the cognitive impairment
Changes in dietetic habits
Changes in Barthel score
Changes in Morisky-Green score
changes in weight
Number of adverse events
Number of adverse events related or nonrelated to the study or placebo products.

Full Information

First Posted
May 8, 2016
Last Updated
June 1, 2016
Sponsor
Team Foods Colombia S.A.
Collaborators
Biopolis S.L.
search

1. Study Identification

Unique Protocol Identification Number
NCT02778581
Brief Title
Study to Evaluate the Effect of a Vegetal Oil on Cognitive Impairment
Official Title
Randomized, Double Blind, Placebo Controlled Prospective Study, to Evaluate the Effect of a Vegetal Oil in the Disease's Natural Evolution in Patients Diagnosed With Cognitive Impairment or Mild to Moderate Alzheimer Disease.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Unknown status
Study Start Date
March 2016 (undefined)
Primary Completion Date
April 2017 (Anticipated)
Study Completion Date
July 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Team Foods Colombia S.A.
Collaborators
Biopolis S.L.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of the study is to evaluate the beneficial effect of a mixture of vegetal oils with a composition related to short, medium and long unsaturated chain fatty acids on patients with a diagnose of cognitive impairment or mild to moderate Alzheimer disease
Detailed Description
The cognitive impairment syndrome is defined as a decrease of the intellectual performance with respect to a previous step in time. The Cognitive impairment has to be considered as a functional alteration with a continuous and physiological evolution in which happen a set of different circumstances: A increasing and normal reduction, that appears after the age of sixty, also known as Age-associated memory impairment (AAMI) A mild cognitive impairment (MCI), with a recent and mild loss of memory, but higher to that expected because of patient's age and educational level. A severe pathological decrease of the mental abilities, also known as, depending on its characteristics: Severe cognitive impairment (SCI), senile dementia and Alzheimer's disease (1). In the next years it is expected that this disease will become one of the main health and aged-related problem in aged people.(2) Nowadays, there are 35,6 million people with any kind of dementia, and it is estimated that every year, 7,7 million of new patients are diagnosed. (3) The amount of people affected will probably duplicate every 20 years, if effective treatments to stop its evolution are not developed. The forecast estimate up to 81,1 million of patients in 2040, which make this disease in a XXI century real epidemic.(4) Before reaching the level of dementia, SCI or Alzheimer's disease, the patient will suffer a progressive mild cognitive impairment. In this level, the disease can be early diagnosed and it would be worth to act on it. Evidences of the Polyunsaturated oils use on the prevention and/or treatment of cognitive impairment. Polyunsaturated fatty acids (PUFA) can help to improve the cognitive functions. Neuronal tissues, as the brain, retina and the neurone-covering membranes (myelin) include high levels of PUFA. (5) PUFA's act on the order transmission in the Nervous System. Population studies reported the beneficial effect of fish oil, with a high PUFA concentration, on the memory of patients suffering a mild cognitive impairment. (6) It can be also beneficial for Alzheimer's patients, as they are deficient in PUFA's. A diet rich in PUFA'S can improve the cognitive function on patients con cognitive impairment and Alzheimer's disease. (6-8) Epidemiological studies suggest that oils rich in short chain PUFA, should play a beneficial role stopping the initial progression of Alzheimer's disease. The previous data confirm the possibility of a beneficial effect of the product to study (a mixture of vegetable oils, rich in triglyceride and lecithins) due to the common characteristic of the product with those PUFA's already marketed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cognitive Impairments, Alzheimer Disease
Keywords
Cognitive Impairment, Alzheimer's Disease, Vegetal Oil

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Lipidic Blend 1
Arm Type
Active Comparator
Arm Description
Glass bottle with 45 ml of vegetal mixture oil. 1 bottle per day
Arm Title
Lipidic Blend 2
Arm Type
Active Comparator
Arm Description
Glass bottle with 45 ml of vegetal mixture oil. 1 bottle per day
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Glass bottle with 45 ml of Olive oil. 1 bottle per day
Intervention Type
Dietary Supplement
Intervention Name(s)
Lipidic Blend 1
Intervention Description
daily intake of the content of one 45 mL bottle containing the product
Intervention Type
Dietary Supplement
Intervention Name(s)
Lipidic Blend 2
Intervention Description
daily intake of the content of one 45 mL bottle containing the product
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
daily intake of the content of one 45 mL bottle containing olive oil
Primary Outcome Measure Information:
Title
Changes in Mini-Mental State Examination (MMSE) score
Time Frame
baseline, 3 month, 6 month, 9 month, 12 month
Title
Changes in Global Clinical Dementia Rating (CDR) score
Time Frame
baseline, 3 month, 6 month, 9 month, 12 month
Secondary Outcome Measure Information:
Title
Changes in systemic oxidative parameters in periferic blood samples (Nitric Oxyde)
Time Frame
baseline, 12 month
Title
Changes in systemic oxidative parameters in periferic blood samples (Malondialdehyde (MDA))
Time Frame
baseline, 12 month
Title
Changes in beta-amyloid protein concentration
Description
Changes in mean values on high sensitivity beta-amyloid 1-40 and 1-42 protein and TAU-protein in cerebrospinal fluid on those patients with a new diagnose of mild to moderate cognitive impairment, that require an initial lumbar puncture and a new lumbar puncture to control evolution at the end of teh study.
Time Frame
baseline, 12 month
Title
Changes in TAU-Protein concentration
Description
Changes in mean values on high sensitivity beta-amyloid 1-40 and 1-42 protein and TAU-protein in cerebrospinal fluid on those patients with a new diagnose of mild to moderate cognitive impairment, that require an initial lumbar puncture and a new lumbar puncture to control evolution at the end of teh study.
Time Frame
baseline, 12 month
Title
Changes in regular treatment for the cognitive impairment
Time Frame
baseline, 3 month, 6 month, 9 month, 12 month
Title
Changes in dietetic habits
Time Frame
baseline, 3 month, 6 month, 9 month, 12 month
Title
Changes in Barthel score
Time Frame
baseline, 3 month, 6 month, 9 month, 12 month
Title
Changes in Morisky-Green score
Time Frame
baseline, 3 month, 6 month, 9 month, 12 month
Title
changes in weight
Time Frame
baseline, 3 month, 6 month, 9 month, 12 month
Title
Number of adverse events
Description
Number of adverse events related or nonrelated to the study or placebo products.
Time Frame
baseline, 3 month, 6 month, 9 month, 12 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
55 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: informed consents signed by patients and/or caretaker The patient has to fulfil dementia clinical criteria. Age between 55 and 85 years old. MMSE score between 18 and 26. The patient can fulfil all neuropsychologic test, according to investigator. The patient has to be always with his/her caretaker during monitorization visits The caretaker has to be in regular contact with the patient, knowing his/her situation and participation in the study. The caretaker has to check four times per week, at least, the product intake, as well as the routine medication and his/her dietetic habits. Both caretaker and patient have to be able to complete the product intake during all the length of the study, according to the main investigator. Exclusion Criteria: Patient and/or caretaker not being able to understand and agree in writing their participation in the study. Patient disability to oral intake of products. Known allergy to any of the product components (active and placebo) Evidence of suffering other neuropsychiatric disturbances apart of dementia as: Parkinson disease, psychotic disturbance, bipolar depression. regular intake of alcohol higher than 45 g ethanol/day, during the year before study inclusion. Any known concurrent malignant pathology in the moment of study inclusion, or severe metabolic, cardiovascular, renal, hepatic, or gastrointestinal disease that cannot allow the ending of the study according the investigator. Any analytical abnormality during the screening, apart from: Creatinine no less than 1.7 mg/dL; low levels of Vitamin B12, and TSH abnormal values.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Vicente Navarro-López, MD
Email
vnavarro@ucam.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Miguel A Carrión-Gutiérrez, PhD
Email
miguelcarrion65@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vicente Navarro-López, MD
Organizational Affiliation
Universidad Católica San Antonio de Murcia
Official's Role
Study Director
Facility Information:
Facility Name
Hospital Universitario Vinalopó
City
Elche
State/Province
Alicante
ZIP/Postal Code
03293
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ana Fríes-Ramos, MD
Email
afries@vinaloposalud.com
Facility Name
Hospital Universitario de Torrevieja
City
Torrevieja,
State/Province
Alicante
ZIP/Postal Code
03186
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rosa Vela-Yebra, MD
Email
rvela@torrevieja-salud.com
First Name & Middle Initial & Last Name & Degree
María A Méndez-Miralles, MD
Email
mamendez@torrevieja-salud.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
22792378
Citation
Kueider AM, Parisi JM, Gross AL, Rebok GW. Computerized cognitive training with older adults: a systematic review. PLoS One. 2012;7(7):e40588. doi: 10.1371/journal.pone.0040588. Epub 2012 Jul 11.
Results Reference
background
PubMed Identifier
20150735
Citation
Luck T, Luppa M, Briel S, Riedel-Heller SG. Incidence of mild cognitive impairment: a systematic review. Dement Geriatr Cogn Disord. 2010;29(2):164-75. doi: 10.1159/000272424. Epub 2010 Feb 11.
Results Reference
background
Citation
Coronado M, et al. Los ácidos grasos omega-3 y omega-6: Nutrición, bioquímica y salud. REB 25(3) 2006: 72-79
Results Reference
background
PubMed Identifier
22332096
Citation
Swanson D, Block R, Mousa SA. Omega-3 fatty acids EPA and DHA: health benefits throughout life. Adv Nutr. 2012 Jan;3(1):1-7. doi: 10.3945/an.111.000893. Epub 2012 Jan 5.
Results Reference
background
PubMed Identifier
22932777
Citation
Lee LK, Shahar S, Chin AV, Yusoff NA. Docosahexaenoic acid-concentrated fish oil supplementation in subjects with mild cognitive impairment (MCI): a 12-month randomised, double-blind, placebo-controlled trial. Psychopharmacology (Berl). 2013 Feb;225(3):605-12. doi: 10.1007/s00213-012-2848-0. Epub 2012 Aug 30.
Results Reference
background
PubMed Identifier
15543423
Citation
Larrieu S, Letenneur L, Berr C, Dartigues JF, Ritchie K, Alperovitch A, Tavernier B, Barberger-Gateau P. Sociodemographic differences in dietary habits in a population-based sample of elderly subjects: the 3C study. J Nutr Health Aging. 2004;8(6):497-502.
Results Reference
background
PubMed Identifier
17435956
Citation
Gillette Guyonnet S, Abellan Van Kan G, Andrieu S, Barberger Gateau P, Berr C, Bonnefoy M, Dartigues JF, de Groot L, Ferry M, Galan P, Hercberg S, Jeandel C, Morris MC, Nourhashemi F, Payette H, Poulain JP, Portet F, Roussel AM, Ritz P, Rolland Y, Vellas B. IANA task force on nutrition and cognitive decline with aging. J Nutr Health Aging. 2007 Mar-Apr;11(2):132-52.
Results Reference
background
PubMed Identifier
14653768
Citation
Logan AC. Neurobehavioral aspects of omega-3 fatty acids: possible mechanisms and therapeutic value in major depression. Altern Med Rev. 2003 Nov;8(4):410-25.
Results Reference
background
PubMed Identifier
15129302
Citation
Bourre JM. Roles of unsaturated fatty acids (especially omega-3 fatty acids) in the brain at various ages and during ageing. J Nutr Health Aging. 2004;8(3):163-74.
Results Reference
background
Links:
URL
http://www.who.int/mediacentre/factsheets/fs362/en/
Description
World Health Organization. Dementia. Fact sheet 362. Published March 2015
URL
http://www.uv.es/aprjuv/quaderns/deterioro.pdf
Description
El deterioro cognitivo leve (DCL) en la edad de oro

Learn more about this trial

Study to Evaluate the Effect of a Vegetal Oil on Cognitive Impairment

We'll reach out to this number within 24 hrs