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PerformanceNCT06982326

Mental Fatigue and Performance in Young Soccer Players

A study testing MF+ and MF- in people with Performance and Soccer, run by Tokat Gaziosmanpasa University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The study employed a randomized, parallel-group, between-subjects design in which participants were assigned to either the MF+ or MF- condition and completed a single testing session accordingly. Read more about this study

Who is it for?
Ages 15 to 16 years, men onlyHealthy volunteers can take part
Conditions the study is for
Performance, Soccer, Mental Fatigue
What is being tested?
MF+ and MF-
Could I receive a placebo?
No, everyone receives an active treatment
How many people
16 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Mar 2025to 30 Mar 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 15 to 16 years
  • Men only
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • Being healthy
  • Male soccer players
  • Willing to maintain the intervention for all sessions

Who cannot join

  • Being under 14 years old
  • Having a chronic disease
  • Contraindications for exercise

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Tokat Gaziosmanpasa Universty

    Tokat Province, Turkey, 6000

Other trials in Turkey (Türkiye)

About this study

Official title: Investigation of the Effects of Mental Fatigue on Physical Performance and Perceived Psychophysiological Reactions in Young Soccer Players: A Field Based Study

The study employed a randomized, parallel-group, between-subjects design in which participants were assigned to either the MF+ or MF- condition and completed a single testing session accordingly. All test sessions were conducted on synthetic turf pitches and comprised three stages of testing, which included assessments of aerobic and anaerobic endurance, jumping, agility, and balance. During the familiarization session, players were briefed on the study procedures, practiced the main tasks, and became accustomed to the equipment and environment used during the intervention. During the MF+ session, prior to each physical testing stage, participants completed a 30-minute Color-word Stroop task (CST) to induce MF. To minimize external influence, players were not prompted or verbally encouraged during testing. Immediately, after each session, ratings of perceived exertion (RPE 6--20) were recorded using the category-level Borg scale (29), and enjoyment was assessed using the exercise enjoyment scale, a bipolar instrument consisting of eight items scored on a 1-7 Likert scale.

Read the detailed description

The study employed a randomized, parallel-group, between-subjects design in which participants were assigned to either the MF+ or MF- condition and completed a single testing session accordingly. Players were recommended to sleep for at least 7-8 hours, refrain from exercising at moderate to high intensity, and avoid consuming alcoholic or caffeinated beverages during the 24 hours before the intervention. Indoor and outdoor temperatures (25-28°C) and humidity levels (35-40%) were kept consistent across all intervention sessions. All test sessions were conducted on synthetic turf pitches and comprised three stages of testing, which included assessments of aerobic and anaerobic endurance, jumping, agility, and balance. During the familiarization session, players were briefed on the study procedures, practiced the main tasks, and became accustomed to the equipment and environment used during the intervention. During the MF+ session, prior to each physical testing stage, participants completed a 30-minute Color-word Stroop task (CST) to induce MF. Four color words (red, blue, green, and yellow) were randomly printed, and participants were required to verbally name the color of each word. During the control (MF-) session, prior to each physical testing stage, participants watched emotionally neutral documentaries for 30 minutes. Each testing session began with a standardized 15-minute warm-up, consisting of 5 minutes of low- to moderate-intensity running followed by 10 minutes of upper- and lower-extremity-specific dynamic stretching, mobility exercises, and change-of-direction drills. To minimize external influence, players were not prompted or verbally encouraged during testing. Immediately, after each session, ratings of perceived exertion (RPE 6--20) were recorded using the category-level Borg scale, and enjoyment was assessed using the exercise enjoyment scale, a bipolar instrument consisting of eight items scored on a 1-7 Likert scale.

Being tested
MF+, MF-
Keywords
Neuromuscular control, Fatigue, Cognitive fatigue, Soccer performance
Medical subject headings
Mental Fatigue, Fatigue

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • MF+Other

    During the MF+ session, before each physical testing phase, participants completed a 30-min Colour Word Stroop task (CST) to trigger MF. The paper-based version of the CST was completed in quiet rooms following the same protocol as in previous studies. This prolonged cognitive task was reported to require sustained attention and automatic response inhibition and effectively induced MF through cognitive manipulation. ThyIt had ben Four colour words (red, blue, green and yellow) were randomly printed and participants were asked to verbalise the colour of each word.

  • MF-Other

    During the control session, before each physical testing phase, participants watched emotionally neutral documentaries for 30 min.

Study groups in NCT06982326
Study groupRoleWhat they receive
Mental Fatigue (MF+)OtherDuring the MF+ session, before each physical testing phase, participants completed a 30-min Colour Word Stroop task (CST) to trigger
Receives: Other: MF+
Control (MF-)OtherControl
Receives: Other: MF-

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Aerobic performance assessment

    The test consisted of shuttle runs between two landmarks placed 20 metres apart, and athletes were required to complete a short active recovery period by running or walking within 10 seconds after each shuttle run. The testing protocol typically includes a standardised warm-up followed by progressive shuttle runs until exhaustion. The distance travelled or the level reached before exhaustion is used to measure performance. The test was carried out on an artificial turf field according to the recommended procedures.

    Measured: From baseline to the end of measurement at 1 day

  2. Countermovement jump performance assessment

    Countermovement jump tests with arms free (CMJf) tests were used to test the performance of the players in the vertical jump test. Each player's CMJf jump height was measured via Optojump photoelectric cells (Microgate, Bolzano, Italy). To ensure proper recovery and reduce fatigue, players were given a passive rest period of 2 minutes between consecutive trials in the same jump test. In addition, there was a rest period of 5 min between the different jump tests.

    Measured: From baseline to the end of measurement at 1 day

  3. Agility performance assessment

    Players completed three Zig-Zag agility tests with a ball (ZZwB) on a synthetic turf field. Each set was followed by a 3-minute recovery period, and the fastest time recorded from all sets was considered to be the performance of the test. The ZZwB trail comprises four 5-meter sections designed at 100° angles. In a previous study by Mirkov et al. (34), a coefficient of variation of 21.12%, intraclass correlation coefficients (ICCs) of 0.81 and 0.84, and typical measurement errors of 0.21 and 0.098 were reported for ZZwB.

    Measured: From baseline to the end of measurement at 1 day

  4. Balence performance assessment

    The Y balance test was used for balance measurements. Before the test, the length of both legs of each player was measured via a standard tape measure from the anterior superior iliac spine to the most distal medial malleolus in the supine position. The test, consisting of three different directions of movement (anterior, posteromedial, and posterolateral), was used to assess dynamic balance with a single-leg stance while reaching these directions. After six trials on each foot for familiarization, each player performed three successful reaches 15 s apart. After the test, the composite score (CS) was calculated via the following formula (37): CS = [(maximum anterior reach + maximum posteromedial reach + maximum posterolateral reach)/(leg length × 3)] × 100.

    Measured: From baseline to the end of measurement at 1 day

  5. Anaerobic Endurance assessment

    A three-corner run test (TCRT) was used to assess the speed and anaerobic endurance of the players. After the start signal, the players ran to a flagpole 80 m away from the start. The players then turned to the left side and ran to a flagpole, 20 m away from flagpole. After that, the players returned to flagpole 82.4 m from the start. Finally, turning to the right, the players ran to finish line and crossed the line to end the test.

    Measured: From baseline to the end of measurement at 1 day

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 May 2025
  2. Study start1 Mar 2025
  3. Primary completion27 Mar 2025
  4. Study completion30 Mar 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Crossover
Model description
Crossover Assignment
Masking
Single blind
Who is masked
Participant
Enrolment
16 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06982326
Sponsor's protocol ID
UGaziosmanpasa-3
Status last verified
May 2025
First submitted
13 May 2025
Last updated
21 May 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Arslan E, Soylu Y, Clemente FM, Hazir T, Kin Isler A, Kilit B. Short-term effects of on-field combined core strength and small-sided games training on physical performance in young soccer players. Biol Sport. 2021 Oct;38(4):609-616. doi: 10.5114/biolsport.2021.102865. Epub 2021 Feb 11.

    PubMed 34937971
  • Soylu Y, Ramazanoglu F, Arslan E, Clemente FM. Effects of mental fatigue on the psychophysiological responses, kinematic profiles, and technical performance in different small-sided soccer games. Biol Sport. 2022 Oct;39(4):965-972. doi: 10.5114/biolsport.2022.110746. Epub 2021 Dec 30.

    PubMed 36247954

Questions about this trial

What is this clinical trial studying?

A study testing MF+ and MF- in people with Performance and Soccer, run by Tokat Gaziosmanpasa University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 21 May 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Aerobic performance assessment (time frame: From baseline to the end of measurement at 1 day). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06982326, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 May 2025.

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