NCT06619249

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
24

participants targeted

Target at below P25 for phase_4

Timeline
3mo left

Started Aug 2024

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress88%
Aug 2024Jul 2026

First Submitted

Initial submission to the registry

August 6, 2024

Completed
17 days until next milestone

Study Start

First participant enrolled

August 23, 2024

Completed
1 month until next milestone

First Posted

Study publicly available on registry

October 1, 2024

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 21, 2025

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

July 30, 2026

Expected
Last Updated

August 26, 2025

Status Verified

August 1, 2024

Enrollment Period

11 months

First QC Date

August 6, 2024

Last Update Submit

August 19, 2025

Conditions

Keywords

Coenzyme Q10SupplementationMyokineExerkineCognitionLong-distance runners

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

EXPERIMENTAL

The participants will be treated with CoQ10 supplements

Dietary Supplement: CoQ10 supplementation

Placebo-treated participants

PLACEBO COMPARATOR

The participants will be treated with placebo

Dietary Supplement: Placebo supplementation

Interventions

CoQ10 supplementationDIETARY_SUPPLEMENT

Long-distance runners will be supplemented with CoQ10 for 4 weeks in cross-over manner with 4 weeks of wash out period.

CoQ10-treated participants
Placebo supplementationDIETARY_SUPPLEMENT

Long-distance runners will be supplemented with placebo for 4 weeks in cross-over manner with 4 weeks of wash out period.

Placebo-treated participants

Eligibility Criteria

Age30 Years - 50 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

RECRUITING

MeSH Terms

Conditions

Behavior

Study Design

Study Type
interventional
Phase
phase 4
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
CROSSOVER
Model Details: A randomized, double-blind, placebo-controlled, cross-over study
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

Locations