- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06619249
Effect of Endurance Training-Induced Coenzyme Q10 (CoQ10) Supplementation on Myokine, Exerkine Secretion and Cognitive Functions in Long-Distance Runners
The goal of this clinical trial is to learn if CoQ10 amplifies endurance training-induced myokine and exerkine secretion and if those changes influences cognition in long-distance runners.
Does 4-week high-dosage CoQ10 supplementation increase the secretion of myokine, exerkine sercetion? Does the above-mentioned intervention improve the cognitive function in long distance runners?
Participants will:
Take CoQ10 or a placebo every day for 4 weeks. Visit the laboratory once every 4 weeks for checkups and tests. Keep the participants' food and training diary.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Phase 4
Contacts and Locations
Study Locations
-
-
-
Gdansk, Poland, 80-333
- Recruiting
- Gdansk University of Physical Education and Sport
-
Contact:
- Zbigniew Jost, PhD
- Phone Number: +48663892068
- Email: zbigniew.jost@awf.gda.pl
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- training experienced for minimum 2 years
- running training at least 2 times per week
- Personal Best on 10k (<50 minutes)
Exclusion Criteria:
- taking supplements which can interrupt primary outcomes (vitamin D, omega-3 fatty acids)
- injured in last 6 months to avoid n number reduction
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: CoQ10-treated participants
The participants will be treated with CoQ10 supplements
|
Long-distance runners will be supplemented with CoQ10 for 4 weeks in cross-over manner with 4 weeks of wash out period.
|
|
Placebo Comparator: Placebo-treated participants
The participants will be treated with placebo
|
Long-distance runners will be supplemented with placebo for 4 weeks in cross-over manner with 4 weeks of wash out period.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in cognitive funtions as a result of CoQ10 supplementation measured via cogntitive function test.
Time Frame: The investigators are going to check this hypothesis after 4 weeks of high-dose supplementation with CoQ10
|
The investigators assume that supplementation with CoQ10 will change cognition (measured via cognitive function tests - Stroop Test, Trial Making Test A and Trial Making Test B) in long-distance runners.
The results will be obtained as time (seconds) needed to complete tasks while testing.
|
The investigators are going to check this hypothesis after 4 weeks of high-dose supplementation with CoQ10
|
|
Change in myokine and exerkine concentration in the blood plasma as a result of CoQ10 supplementation.
Time Frame: The investigators are going to check this hypothesis after 4 weeks of high-dose supplementation with CoQ10
|
The investigators will assess the concentration of blood myokine and exerkine concentration (pg or ug/dl) of blood plasma using the colorimetric method.
|
The investigators are going to check this hypothesis after 4 weeks of high-dose supplementation with CoQ10
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in aerobic capacity measured via direct test to volitional exhaustion on a motorized treadmill
Time Frame: The investigators are going to check this hypothesis after 4 weeks of high-dose supplementation with CoQ10
|
The investigators assume that supplementation with CoQ10 will change the aerobic capacity (oxygen uptake in ml-1 x min-1 x kg-1) in long-distance runners.
The determination of aerobic capacity will be done through progressive test to volitional exhaustion on a motorized treadmill and gas analyzer
|
The investigators are going to check this hypothesis after 4 weeks of high-dose supplementation with CoQ10
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AWFiS/2024_3_ZJ
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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