- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06683625
Neurotransmitter Analysis, Stress, and Energy Availability in Athletes
Effects of Intense Physical Exertion on Neurotransmitter Levels, Stress, and Recovery in Relation to Energy Availability in Athletes
The goal of this observational study is to examine if there is a correlation between energy deficiency, neurotransmitter levels, and exercise test performance among athletes in the Polish national rowing team. The main questions it aims to answer are:
Does relative energy deficiency (RED) impact neurotransmitter levels and, consequently, athletic performance? Can monitoring energy availability, neurotransmitter levels, and psychological factors provide insights into physiological and psychological adaptations to intense training? Researchers will compare results obtained before the exercise test with those taken immediately after and following a 1-hour recovery period to assess changes in performance, biochemical markers, and psychological responses.
Participants will:
- Engage in a standardized exercise test.
- Undergo assessments of energy availability, neurotransmitter levels, and performance at multiple time points (pre-exercise, immediately post-exercise, and post-1-hour recovery).
- Complete psychological questionnaires assessing stress levels, recovery, and energy availability.
This study aims to identify potential links between energy status, biochemical responses, psychological well-being, and athletic performance, allowing for targeted interventions to optimize training outcomes.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The primary goal of this project is to optimize athletic training for the national rowing team through comprehensive multi-dimensional monitoring. This approach aims to enhance athletes' performance capabilities and readiness for high-level competition. The Polish national rowing team consistently wins medals at international events, with the Olympic medal being the ultimate achievement for these athletes. Given this high standard, special attention is placed on preparing the athletes, not only in terms of physical readiness but also through continuous monitoring of adaptive processes. This proactive approach enables early detection of adverse changes, allowing for rapid adjustments to the training process to prevent fatigue and overtraining.
Building on the previous year's findings, this project focuses on the effects of relative energy deficiency (RED) in sports. Introduced by the International Olympic Committee in 2014, RED refers to a syndrome of impairments that arise from low energy availability (EA) due to an imbalance between energy intake and expenditure relative to lean body mass. In high-performance sports like rowing, athletes experience internal and external pressures to maintain peak performance, which often impacts energy intake and expenditure. Low energy availability (LEA) initially leads to negative energy balance and weight loss, as the body's energy reserves are used to meet demand. Over time, chronic LEA results in metabolic and physiological adaptations, reducing total energy expenditure to prevent further weight loss. While body weight and fat mass may stabilize, athletes can experience compromised physiological functions due to LEA.
LEA impacts recovery, muscle mass, neuromuscular function, and increases injury risk, all of which can detrimentally affect performance. Sustained LEA aimed at reducing body mass or fat levels can lead to health and performance declines, a pattern seen in both male and female athletes. Recent awareness highlights that male rowers, previously assumed to be protected due to their higher lean mass and body size, may also experience RED-S. The demands of high-level rowing, often involving six hours of intense daily training with long endurance sessions and strength workouts, create challenges in meeting energy requirements.
This project involves biochemical assessments alongside psychological questionnaires to monitor athletes' stress, recovery, and energy availability. Such comprehensive monitoring provides insights into both the physical and mental responses to training stressors, supporting the development of tailored interventions for optimal performance and health in elite rowers.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Greater Poland Voivodeship
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Poznan, Greater Poland Voivodeship, Poland, 61-871
- Poznań University of Physical Education
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Gender and Biological Sex Alignment: Participants' self-identified gender must align with their biological sex due to the effects of sexual dimorphism on athletic performance.
Sex: Both male and female athletes are eligible to participate. Training Level: Participants must be highly trained, with a minimum of 5 years of consistent, high-level athletic training experience.
Experience: Participants should have competitive experience at a regional, national, or international level.
Health Status: Participants must be healthy, with no current or chronic medical conditions, injuries, or diseases that could affect study outcomes.
Exclusion Criteria:
- Gender-Biological Sex Mismatch: Individuals whose self-identified gender does not align with their biological sex are excluded, to maintain consistency in data affected by sexual dimorphism.
Training Level: Recreational athletes, individuals with less than 3 years of high-level training, or those lacking competitive experience are excluded.
Health Conditions: Individuals with any medical conditions, chronic illnesses, acute injuries, or undergoing treatments that may interfere with athletic performance or study variables are excluded.
Medication: Use of medications or supplements that could influence metabolism, muscle composition, or overall physical performance results in exclusion.
Other Factors: Any other factors, such as lifestyle habits (e.g., smoking, excessive alcohol use), that could affect physiological responses to training and testing, are grounds for exclusion.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Group 1
Eight female athletes
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"6K Max Effort Erg Test", involves participants completing a 6000-meter rowing distance on an ergometer as quickly as possible.
This test is designed to measure peak endurance and performance under controlled conditions and will serve as a primary assessment of each athlete's physical output and adaptive capacity.
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Group 2
19 male athletes
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"6K Max Effort Erg Test", involves participants completing a 6000-meter rowing distance on an ergometer as quickly as possible.
This test is designed to measure peak endurance and performance under controlled conditions and will serve as a primary assessment of each athlete's physical output and adaptive capacity.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Changes from baseline in cortisol level.
Time Frame: At rest (before the exercise test), 1 minute after the end of the test, after 1 hour of recovery.
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Marker of stress level.
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At rest (before the exercise test), 1 minute after the end of the test, after 1 hour of recovery.
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Changes from baseline in testosterone level.
Time Frame: At rest (before the exercise test), 1 minute after the end of the test, after 1 hour of recovery.
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Marker of anabolic activity.
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At rest (before the exercise test), 1 minute after the end of the test, after 1 hour of recovery.
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Changes from baseline in serotonin level.
Time Frame: At rest (before the exercise test), 1 minute after the end of the test, after 1 hour of recovery.
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Marker of mood regulation and emotional well-being
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At rest (before the exercise test), 1 minute after the end of the test, after 1 hour of recovery.
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Changes from in serotonin level.
Time Frame: At rest (before the exercise test), 1 minute after the end of the test, after 1 hour of recovery.
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Marker of mood regulation and emotional well-being.
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At rest (before the exercise test), 1 minute after the end of the test, after 1 hour of recovery.
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Changes from baseline in gamma-aminobutyric acid (GABA) level.
Time Frame: At rest (before the exercise test), 1 minute after the end of the test, after 1 hour of recovery.
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Marker of neuroinhibition.
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At rest (before the exercise test), 1 minute after the end of the test, after 1 hour of recovery.
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Changes from baseline in dopamine level.
Time Frame: At rest (before the exercise test), 1 minute after the end of the test, after 1 hour of recovery.
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Marker of stress and adrenal function.
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At rest (before the exercise test), 1 minute after the end of the test, after 1 hour of recovery.
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Changes from baseline in tryptophan level.
Time Frame: At rest (before the exercise test), 1 minute after the end of the test, after 1 hour of recovery.
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Marker of mood regulation, serotonin synthesis.
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At rest (before the exercise test), 1 minute after the end of the test, after 1 hour of recovery.
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Baseline Mood Profile of Athletes Before Exercise Test Using POMS Questionnaire.
Time Frame: At rest (before the exercise test).
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The Profile of Mood States (POMS) questionnaire measures mood states and emotional well-being.
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At rest (before the exercise test).
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Baseline Stress and Recovery Profile of Athletes Before Exercise Test Using RESTQ-76 Sport Questionnaire.
Time Frame: At rest (before the exercise test).
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The Recovery-Stress Questionnaire for Athletes (RESTQ-76 SPORT), 76-item version questionnaire measures stress and recovery balance in athletes.
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At rest (before the exercise test).
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Baseline Psychological Strain Assessment of Athletes Before Exercise Test Using APSQ Questionnaire.
Time Frame: At rest (before the exercise test).
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The Athlete Psychological Strain Questionnaire (APSQ) measures psychological strain and mental health challenges in athletes.
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At rest (before the exercise test).
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Baseline Eating Behavior and Attitudes of Athletes Before Exercise Test Using EDE-Q 6.0 Questionnaire.
Time Frame: At rest (before the exercise test).
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The Eating Disorder Examination Questionnaire (EDE-Q 6.0) measures the severity of eating disorder behaviors and attitudes.
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At rest (before the exercise test).
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Baseline Eating Behavior and Attitudes of Athletes Before Exercise Test Using EDE-Q 6.0 Questionnaire.
Time Frame: At rest (before the exercise test).
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The Eating Disorder Examination Questionnaire (EDE-Q) measures the severity of eating disorder behaviors and attitudes.
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At rest (before the exercise test).
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Baseline Energy Availability and Health Assessment of Female Athletes Before Exercise Test Using LEAF Questionnaire.
Time Frame: At rest (before the exercise test).
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The Eating Disorder Examination Questionnaire (EDE-Q) measures the severity of eating disorder behaviors and attitudes.
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At rest (before the exercise test).
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Baseline Energy Availability and Health Assessment of Male Athletes Before Exercise Test Using LEAM Questionnaire.
Time Frame: At rest (before the exercise test).
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The Eating Disorder Examination Questionnaire (EDE-Q) measures the severity of eating disorder behaviors and attitudes.
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At rest (before the exercise test).
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Baseline Dietary Habits Assessment of Athletes Before Exercise Test Using Nutrition Questionnaire
Time Frame: At rest (before the exercise test).
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The nutrition questionnaire assesses dietary habits, nutrient intake, meal frequency and types, potential deficiencies or excesses, food preferences, supplement use, and overall diet quality.
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At rest (before the exercise test).
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Baseline Body Composition Assessment of Athletes Before Exercise Test
Time Frame: At rest (before the exercise test).
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Baseline body composition measurements will be conducted using the bioimpedance method to assess athletes' body fat, muscle mass, and overall composition prior to the exercise test.
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At rest (before the exercise test).
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RowersMF2024
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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