Parkinson Disease Clinical Trial
— PARKAOfficial title:
Effect of Exercise, Endocannabinoids and Ketones on Cerebral Metabolism in a Cognitive Disorders Population : Pilot Project PARKA
Verified date | May 2024 |
Source | Université de Sherbrooke |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
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. |
Country | Name | City | State |
---|---|---|---|
Canada | Centre de recherche sur le vieillissement | Sherbrooke | Quebec |
Lead Sponsor | Collaborator |
---|---|
Université de Sherbrooke | Société des Produits Nestlé (SPN) |
Canada,
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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