Your session is about to expire
← Back to Search
Medium Chain Triglycerides (MCTs)
Exercise + MCT Supplement for Cognitive Disorders (PARKA Trial)
N/A
Waitlist Available
Led By Stephen Cunnane, Ph.D.
Research Sponsored by Université de Sherbrooke
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Alzheimer's or Parkinson disease diagnostic
Be older than 18 years old
Must not have
MMSE less than 20
MCT or coconut oil supplementation
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 months, evaluation before and after intervention
Awards & highlights
No Placebo-Only Group
Summary
This trial involves patients with Parkinson's and Alzheimer's taking a fat supplement regularly and doing guided exercises to improve brain function and overall health.
Who is the study for?
This trial is for individuals with Alzheimer's or Parkinson's disease who can consent, have stable medication, and an accompanying person for visits. They must be able to read and speak French. Excluded are those already physically active, with metal implants, low MMSE scores, MCT/coconut use or allergy, uncontrolled diseases that could interfere, cardiac issues, inability to lay flat for 40 minutes, or substance use.
What is being tested?
The study tests the effects of a commercial MCT supplement (50g/day) combined with supervised aerobic exercise three times weekly on cognition and ketone levels in people with cognitive disorders from Parkinson's and Alzheimer's over two months. It also measures endocannabinoids plasma concentrations before and after intervention.
What are the potential side effects?
Potential side effects may include gastrointestinal discomfort due to the MCT supplement intake such as diarrhea or cramps; however specific side effects will be monitored throughout the study.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have been diagnosed with Alzheimer's or Parkinson's disease.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
My memory and thinking skills are significantly impaired.
Select...
I am taking MCT or coconut oil supplements.
Select...
I cannot lie on my back for 40 minutes.
Select...
I use cannabis, THC, or CBD.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 months, evaluation before and after intervention
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 months, evaluation before and after intervention
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Cognition
Ketones
Secondary study objectives
Endocannabinoids
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Group I: Parkinson diseaseExperimental Treatment1 Intervention
2 months intervention with 50g/day of a commercial MCT supplement combine with supervised aerobic exercise 3x/week.
Group II: Alzheimer's diseaseExperimental Treatment1 Intervention
2 months intervention with 50g/day of a commercial MCT supplement combine with supervised aerobic exercise 3x/week.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Parkinson's Disease (PD) often target mitochondrial dysfunction and oxidative stress, which are key contributors to neurodegeneration in PD. MCT supplements increase ketone production, providing an alternative energy source that may enhance mitochondrial function and reduce oxidative stress.
Aerobic exercise improves brain health by increasing blood flow, promoting neuroplasticity, and reducing inflammation. These mechanisms are crucial for PD patients as they help protect dopaminergic neurons, potentially slowing disease progression and improving motor and cognitive functions.
The Anti-Inflammatory Effect of Preventive Intervention with Ketogenic Diet Mediated by the Histone Acetylation of <i>mGluR5</i> Promotor Region in Rat Parkinson's Disease Model: A Dual-Tracer PET Study.Increased Beta-Hydroxybutyrate Level Is Not Sufficient for the Neuroprotective Effect of Long-Term Ketogenic Diet in an Animal Model of Early Parkinson's Disease. Exploration of Brain and Liver Energy Metabolism Markers.Is NADH effective in the treatment of Parkinson's disease?
The Anti-Inflammatory Effect of Preventive Intervention with Ketogenic Diet Mediated by the Histone Acetylation of <i>mGluR5</i> Promotor Region in Rat Parkinson's Disease Model: A Dual-Tracer PET Study.Increased Beta-Hydroxybutyrate Level Is Not Sufficient for the Neuroprotective Effect of Long-Term Ketogenic Diet in an Animal Model of Early Parkinson's Disease. Exploration of Brain and Liver Energy Metabolism Markers.Is NADH effective in the treatment of Parkinson's disease?
Find a Location
Who is running the clinical trial?
Société des Produits Nestlé (SPN)Industry Sponsor
343 Previous Clinical Trials
62,675 Total Patients Enrolled
Université de SherbrookeLead Sponsor
304 Previous Clinical Trials
76,715 Total Patients Enrolled
NestléIndustry Sponsor
321 Previous Clinical Trials
60,549 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I do not have any uncontrolled conditions that could affect the study.My memory and thinking skills are significantly impaired.I will bring someone with me for the first and last visit.My medication for the condition has not changed recently.I am taking MCT or coconut oil supplements.I cannot lie on my back for 40 minutes.I have been diagnosed with Alzheimer's or Parkinson's disease.I have a heart condition.I can read and speak French.I use cannabis, THC, or CBD.
Research Study Groups:
This trial has the following groups:- Group 1: Alzheimer's disease
- Group 2: Parkinson disease
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Share this study with friends
Copy Link
Messenger