DICe: The Effect of Vegetable Oil on Cognitive Functions of MCI Patients

Sponsor
Bournemouth University (Other)
Overall Status
Completed
CT.gov ID
NCT03727386
Collaborator
Dorset HealthCare University NHS Foundation Trust (Other)
34
1
2
17.5
1.9

Study Details

Study Description

Brief Summary

This study explores the feasibility of applying an intervention using vegetable oils (coconut and sunflower oils) on individuals diagnosed with Mild Cognitive Impairment. Participants will be divided into two groups and will either receive 30 ml of coconut or sunflower oil to be consumed daily for six months.

Condition or Disease Intervention/Treatment Phase
  • Other: Coconut oil
  • Other: Sunflower oil
N/A

Detailed Description

Research has shown that some forms of dementia associated to ageing can often be linked to low levels of sugar in the brain. Which may cause damage to the brain nerve cells. The main source of fuel for the brain comes from sugar in the form of glucose. Providing an additional source of fuel to brain cells may reduce the damage, potentially preventing further decline of dementia in individuals with Mild Cognitive Impairment (MCI).

This study explores the possibility of using vegetable oils (coconut and sunflower oils) as an additional source of energy to individuals diagnosed with Mild Cognitive Impairment. The researchers will use different tests to evaluate if the study could be done. Participants will be divided into two groups and will either receive 30 ml of coconut or sunflower oil to be consumed daily for six months. The researchers will visit participants in their houses over three times during the study to collect the data.

During each visit, the researcher will conduct blood test in which blood will be collected by pricking the finger of participants to check their blood ketone levels. Paper pencil and/or computer tasks will be completed to measure the cognitive abilities (e.g. attention, orientation and learning) of participants. Participants will also be asked to complete a food diary in which they will provide details of their diet and eating habits. Moreover, they will be asked to provide feedback on the study by answering a set of questions either during an interview or by completing a feedback form. The information collected during these visits will be used to evaluate the study.

Results from this study would help determine whether such an intervention can be undertaken in adults with MCI. The study will provide information related to the practicality of using vegetable oils on adults with MCI. This would provide the evidence to develop a larger study that would allow us to systematically evaluate the effect of vegetable oils on MCI. Which would further enable us to develop an intervention that might possibly improve the brain functions of adults with MCI and maintain their quality of life for longer by delaying the development of dementia and reducing the progression from MCI to AD (Alzheimer's disease) in adults.

Study Design

Study Type:
Interventional
Actual Enrollment :
34 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This study will be a pilot study with an internal feasibility study that aims at evaluating the acceptance and adherence of participants to the intervention. Participants will be randomized into an intervention (coconut oil) and control group (sunflower oil) using an online randomisation software; Sealed envelope.This study will be a pilot study with an internal feasibility study that aims at evaluating the acceptance and adherence of participants to the intervention. Participants will be randomized into an intervention (coconut oil) and control group (sunflower oil) using an online randomisation software; Sealed envelope.
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
A Study Evaluating the Feasibility of Undertaking an Intervention Looking Into the Effect of Vegetable Oils Intake on Cognition and Quality of Life in Adults With Mild Cognitive Impairment.
Actual Study Start Date :
Nov 19, 2019
Actual Primary Completion Date :
May 6, 2021
Actual Study Completion Date :
May 6, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Coconut oil

A dietary intervention that relies on the administration of 30 ml of extra virgin coconut oil per day for six months will be utilized in this study. Coconut oil administered will replace the cooking/vegetable oil usually used by the participants. .

Other: Coconut oil
Participants will receive 30 ml of virgin coconut oil to replace their normal oil intake for a period of 6 months.
Other Names:
  • extra virgin coconut oil
  • Placebo Comparator: Sunflower oil

    A dietary intervention that relies on the administration of 30 ml of sunflower oil per day for 6 months will be utilized in this study. The oil administered will replace the cooking/vegetable oil usually used by the participants.

    Other: Sunflower oil
    Participants will receive 30 ml of sunflower oil to replace their normal oil intake for a period of 6 months.

    Outcome Measures

    Primary Outcome Measures

    1. Vegetable oil usage [6 months]

      the amount of oil used by individuals (ml) will be monitored

    Secondary Outcome Measures

    1. Overall cognition [Six months]

      Assessed by Mini Addenbrookes Cognitive Examination (mACE) which has a high score of 30 with higher scores indicating better cognition.

    2. Quality of life of adults with Mild cognitive impairment measured by ADCS-MCI-ADL (Alzheimer's Disease Cooperative Study Mild Cognitive Impairment- Activities of Daily Living) [six months]

      Quality of life of participants measured by ADCS-MCI-ADL (Alzheimer's Disease Cooperative Study Mild Cognitive Impairment- Activities of Daily Living) questionnaire, it has a score that rages from 0 to 53; higher score are linked to better quality of life.

    3. Dietary intake assessed by four day food records using Nutritics software [six months]

      Dietary energy and macronutrient (carbohydrate, fat and protein) intake assessed by four day food records using Nutritics software (https://www.nutritics.com/p/references).

    4. Blood samples (beta hydroxyl butyrate): [six months]

      ketone bodies concentrations (mmol) will be assessed by Abbott freestyle Optium Neo, ketone meter.

    5. Executive measure [six months]

      Assessed by trail making test B that has an average score of 75 seconds and a deficient score of > 273 seconds

    6. Verbal Memory [six months]

      Verbal memory will be assessed by word list test which is a subtest of the Wechsler Memory Scale III; the lower the test score the higher the cognitive impairment.

    7. Verbal Fluency [six months]

      Verbal Fluency test in which a score lower than 17 shows cognitive impairment (the higher the score the better the cognition) will be used to determine

    8. Processing Speed [six months]

      Digit symbol test in which lower test scores are correlated with higher impairment will be used to assess processing speed

    9. Attention [six months]

      Digit Span test will be used to assess attention, the lower the score the higher the impairment.

    10. Visual Spatial memory [six months]

      Supermarket task will be used to asses the visual spatial memory of participants, the score depends on the time required to complete the task. Extra time is related to higher cognitive impairment.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Adults with confirmed MCI diagnosis

    • Adults with Negative Apo E4 genotype

    Exclusion Criteria:
    • Adults diagnosed with Alzheimer's Disease (AD)

    • Adults with positive Apo E4 genotype

    • Adults with confirmed diabetes (Type I, Type II) diagnosis

    • Adults with a history of hyper-cholesterolemia (high cholesterol levels) or Dyslipidaemia

    • Adults who are unable to understand written or verbal English

    • Adults diagnosed with Neurological disorders (Parkinson, stroke…)

    • Adults with post traumatic brain injury (tumour, brain surgery, injury…)

    • Patients with major physical impairments (blind, deaf) or those who are unable to use their dominant hand.

    • Adults with coconut allergy.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Bournemouth University Bournemouth Dorset United Kingdom BH1 3LH

    Sponsors and Collaborators

    • Bournemouth University
    • Dorset HealthCare University NHS Foundation Trust

    Investigators

    • Principal Investigator: Raysa EL Zein, MSc, Student
    • Study Director: Jane Murphy Professor, PhD, Professor of Nutrition
    • Study Director: Peter Thomas Professor, PhD, Professor of Health Care Stats & Epidemiology
    • Study Director: Shanti Shanker Doctor, PhD, Lucturer of Psychology

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Bournemouth University
    ClinicalTrials.gov Identifier:
    NCT03727386
    Other Study ID Numbers:
    • 1718/IRASREZ/1
    First Posted:
    Nov 1, 2018
    Last Update Posted:
    Jun 29, 2021
    Last Verified:
    Jun 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 29, 2021