Thyroid Hormone Responses to Repeated Wingate Exercise Versus a Non-Exercising Comparison Group
RWT-THYROID
Free Thyroid Hormone Responses to Repeated Wingate Exercise Versus a Non-Exercising Comparison Group in Male Amateur Soccer Players
1 other identifier
interventional
40
1 country
1
Brief Summary
This two-group, non-randomized study investigated the acute effects of repeated Wingate exercise on free thyroid hormone concentrations in male amateur soccer players. Twenty healthy male amateur soccer players completed a standardized repeated Wingate exercise protocol, and a separate group of twenty male amateur soccer players provided two morning blood samples without exercising. Blood samples were collected immediately before and immediately after the exercise session or the resting interval to determine free triiodothyronine (fT3), free thyroxine (fT4), and thyroid-stimulating hormone (TSH) concentrations. Including a non-exercising comparison group allows the observed changes to be evaluated against the change expected across a comparable interval in the absence of exercise.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jun 2023
Shorter than P25 for not_applicable
1 active site
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 Start
First participant enrolled
June 15, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2023
CompletedFirst Submitted
Initial submission to the registry
August 11, 2026
CompletedFirst Posted
Study publicly available on registry
August 14, 2026
CompletedSeptember 23, 2026
September 1, 2026
15 days
August 11, 2026
September 18, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Serum Free Thyroid Hormone Concentrations (fT3, fT4, and TSH)
The primary outcome was the within-participant change in serum free thyroid hormone concentrations, including free triiodothyronine (fT3), free thyroxine (fT4), and thyroid-stimulating hormone (TSH), measured immediately before and immediately after the repeated Wingate exercise protocol in the exercise group and across a comparable resting interval in the comparison group. Change scores were compared between groups.
Immediately before and immediately after the repeated Wingate exercise session or the resting interval
Study Arms (2)
Repeated Wingate Exercise
EXPERIMENTALParticipants completed a standardized repeated Wingate exercise protocol under laboratory conditions. Blood samples were collected immediately before and immediately after the exercise session to assess acute changes in serum free triiodothyronine (fT3), free thyroxine (fT4), and thyroid-stimulating hormone (TSH).
Comparison group
NO INTERVENTIONParticipants provided two venous blood samples on one morning and performed no exercise between the two samples. Serum free triiodothyronine (fT3), free thyroxine (fT4), and thyroid-stimulating hormone (TSH) were measured in both samples.
Interventions
Participants completed a standardized repeated Wingate exercise protocol under controlled laboratory conditions to investigate the acute effects of high-intensity anaerobic exercise on thyroid hormone responses. Venous blood samples were collected immediately before and immediately after the exercise session to measure serum free triiodothyronine (fT3), free thyroxine (fT4), and thyroid-stimulating hormone (TSH) concentrations.
Eligibility Criteria
You may qualify if:
- Male amateur soccer players.
- Age between 18 and 25 years.
- At least 6 years of licensed soccer experience.
- Actively participating in amateur soccer training.
- Apparently healthy and free from acute or chronic disease on medical history review.
- Willingness to participate and provision of written informed consent.
You may not qualify if:
- Acute illness or musculoskeletal injury at the time of testing.
- Neurological, auditory, visual or vestibular disorder.
- Reduced physical capacity due to injury, or a sedentary lifestyle.
- History of nutritional or pharmacological ergogenic aid use.
- Failure to complete the study procedures or all required blood sample collections.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Inonu Universitylead
Study Sites (1)
Exercise Physiology Laboratory, Faculty of Sport Sciences, Karabuk University
Karabük, Karabük Province, 78050, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Özgür EKEN, PhD
Inonu University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Masking Details
- No masking was used in this study. Participants were aware of their group assignment because the exercise protocol and blood sample collection required direct participant involvement. Laboratory personnel were not blinded to group or to sampling time point.
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assoc. Prof.Dr.
Study Record Dates
First Submitted
August 11, 2026
First Posted
August 14, 2026
Study Start
June 15, 2023
Primary Completion
June 30, 2023
Study Completion
June 30, 2023
Last Updated
September 23, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- ANALYTIC CODE
- Time Frame
- Data will be available from the date of publication, with no planned end date.
- Access Criteria
- Requests should be directed to the corresponding author. Data will be shared with researchers who provide a methodologically sound proposal, subject to applicable ethics approval, participant-consent restrictions, and institutional requirements. A data-use agreement may be required.
De-identified participant-level data and analysis code are available from the corresponding author on reasonable request, subject to applicable ethics, participant-consent, and institutional requirements.