Effect of Endurance Training-Induced Coenzyme Q10 (CoQ10) Supplementation on Myokine, Exerkine Secretion and Cognitive Functions in Long-Distance Runners
1 other identifier
interventional
24
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_4
Started Aug 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 6, 2024
CompletedStudy Start
First participant enrolled
August 23, 2024
CompletedFirst Posted
Study publicly available on registry
October 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 21, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 30, 2026
ExpectedAugust 26, 2025
August 1, 2024
11 months
August 6, 2024
August 19, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Change in cognitive funtions as a result of CoQ10 supplementation measured via cogntitive function test.
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.
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 Outcomes (1)
Change in aerobic capacity measured via direct test to volitional exhaustion on a motorized treadmill
The investigators are going to check this hypothesis after 4 weeks of high-dose supplementation with CoQ10
Study Arms (2)
CoQ10-treated participants
EXPERIMENTALThe participants will be treated with CoQ10 supplements
Placebo-treated participants
PLACEBO COMPARATORThe participants will be treated with placebo
Interventions
Long-distance runners will be supplemented with CoQ10 for 4 weeks in cross-over manner with 4 weeks of wash out period.
Long-distance runners will be supplemented with placebo for 4 weeks in cross-over manner with 4 weeks of wash out period.
Eligibility Criteria
You may qualify if:
- training experienced for minimum 2 years
- running training at least 2 times per week
- Personal Best on 10k (\<50 minutes)
You may not qualify if:
- taking supplements which can interrupt primary outcomes (vitamin D, omega-3 fatty acids)
- injured in last 6 months to avoid n number reduction
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Gdansk University of Physical Education and Sport
Gdansk, 80-333, Poland
MeSH Terms
Conditions
Study Design
- Study Type
- interventional
- Phase
- phase 4
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 6, 2024
First Posted
October 1, 2024
Study Start
August 23, 2024
Primary Completion
July 21, 2025
Study Completion (Estimated)
July 30, 2026
Last Updated
August 26, 2025
Record last verified: 2024-08