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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04322461
Other study ID # 2020-3436
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date May 1, 2022
Est. completion date December 15, 2024

Study information

Verified date May 2024
Source Université de Sherbrooke
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A two months intervention in which two groups of cognitive disorders, Parkinson and Alzheimer's disease, will receive 50g/day of a commercial MCT supplement combined with supervised aerobic exercise 3 times/week. Cognition and ketones will be assess before and after the intervention, along with endocannabinoids plasma concentrations.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 14
Est. completion date December 15, 2024
Est. primary completion date August 15, 2024
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria: - Alzheimer's or parkinson disease diagnostic - Stable medication associated with the disease - Able to consent - Presence of an accompanying person for the first and last visit. - Ability to read and talk in French Exclusion Criteria: - MMSE < 20 - MCT or coconut oil supplementation - Coconut allergy - Cannabis, THC or CBD consumption - Excessive alcohol consumption - Physical activity 3x/week - Presence of an metallic object in the body - Impossibility to lay in dorsal decubitus for 40 minutes - Cardiac disease - Any uncontrolled disease that could interfer with the project.

Study Design


Intervention

Dietary Supplement:
Betaquik MCT supplement
50g/day divided in 3. Breakfast, lunch and dinner

Locations

Country Name City State
Canada Centre de recherche sur le vieillissement Sherbrooke Quebec

Sponsors (2)

Lead Sponsor Collaborator
Université de Sherbrooke Société des Produits Nestlé (SPN)

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cognition Measure of cognition with CANTAB 2 months, evaluation before and after intervention
Primary Ketones Measurement of ketones concentrations 2 months, evaluation before and after intervention
Secondary Endocannabinoids Endocannabinoids plasma concentration 2 months, evaluation before and after intervention
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