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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03727386
Other study ID # 1718/IRASREZ/1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 19, 2019
Est. completion date May 6, 2021

Study information

Verified date June 2021
Source Bournemouth University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date May 6, 2021
Est. primary completion date May 6, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Intervention

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

Locations

Country Name City State
United Kingdom Bournemouth University Bournemouth Dorset

Sponsors (2)

Lead Sponsor Collaborator
Bournemouth University Dorset HealthCare University NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Vegetable oil usage the amount of oil used by individuals (ml) will be monitored 6 months
Secondary Overall cognition Assessed by Mini Addenbrookes Cognitive Examination (mACE) which has a high score of 30 with higher scores indicating better cognition. Six months
Secondary 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) 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. six months
Secondary Dietary intake assessed by four day food records using Nutritics software Dietary energy and macronutrient (carbohydrate, fat and protein) intake assessed by four day food records using Nutritics software (https://www.nutritics.com/p/references). six months
Secondary Blood samples (beta hydroxyl butyrate): ketone bodies concentrations (mmol) will be assessed by Abbott freestyle Optium Neo, ketone meter. six months
Secondary Executive measure Assessed by trail making test B that has an average score of 75 seconds and a deficient score of > 273 seconds six months
Secondary Verbal Memory 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. six months
Secondary Verbal Fluency 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 six months
Secondary Processing Speed Digit symbol test in which lower test scores are correlated with higher impairment will be used to assess processing speed six months
Secondary Attention Digit Span test will be used to assess attention, the lower the score the higher the impairment. six months
Secondary Visual Spatial memory 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. six months
See also
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