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CompletedNCT07920146Updated Nov 5, 2026

Biological Maturation, Athletic Performance, and Injury Risk in Adolescent Male Soccer Players

An observational study in Maturation Level, Football Players and Injuries; Muscle, Nontraumatic, sponsored by Alanya Alaaddin Keykubat University. Completed at 1 site in Turkey (Türkiye). Open to male participants aged 14 Years to 19 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-05.

Sponsored by Alanya Alaaddin Keykubat University · Observational

Updated Nov 5, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
106
Ages
14 Years to 19 Years
Sex
Male
01

Study summary

This study aims to investigate the relationship between biological maturation, athletic performance, and injury risk in adolescent male soccer players. Participants aged 14-19 years will be recruited from a professional soccer academy. Biological maturation status will be assessed using maturity offset calculations, while athletic performance will be evaluated through standardized tests including agility, balance, strength, and aerobic capacity. Injury risk will be assessed using functional movement screening. The findings are expected to provide insights into the role of maturation in performance and injury risk in youth soccer players.

02

Conditions studied

  • Maturation Level
  • Football Players
  • Injuries; Muscle, Nontraumatic
  • Prevention
  • Performance

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Keywords

  • Maturation, injuries, football,performance,prevention
03

In context

Wounds and Injuries

2,217 studies on the registry are indexed under Wounds and Injuries; 441 are open to participants now.

This study's enrollment of 106 is below the median of 169 across 690 observational studies indexed under Wounds and Injuries.

Browse Wounds and Injuries studies →

Lead sponsor

Alanya Alaaddin Keykubat University is the lead sponsor of 51 studies on the registry; 17 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
14 Years to 19 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Adolescent male soccer players aged 14-19 years, actively participating in regular training and competition within a professional soccer academy, will constitute the study population.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Male soccer players aged 14 to 19 years
  • Licensed athletes with at least 1 year of sports experience
  • Actively participating in training and competitions
  • Registered in a professional soccer club academy
  • Able to understand and follow test instructions

Exclusion criteria

Exclusion Criteria:

  • Any health problem occurring during the assessment period
  • Inability to complete performance tests at the required level
  • Irregular participation in study assessments
  • History of surgery within the past year
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
106 participants (actual)
Target follow-up
1 Week
Patient registry
Yes

Groups and cohorts

  • Adolescent Male Football Players

    Participants aged 14-19 years who are actively competing in a professional football academy and undergoing assessment of biological maturation, athletic performance, and injury risk parameters.

    Other: Anthropometric and Performance Assessment.

Interventions

  • OtherAnthropometric and Performance Assessment.

    Participants will undergo a structured evaluation protocol including anthropometric measurements, athletic performance tests (e.g., agility, strength, balance, and aerobic capacity), and injury risk assessment using functional movement screening. No therapeutic or experimental intervention will be applied.

06

What researchers measure

Primary outcomes

  1. Estimated Maturity Offset

    Biological maturation was estimated using the male-specific Mirwald maturity-offset equation based on decimal chronological age, standing height, sitting height, derived leg length, and body mass. Decimal chronological age was calculated using May 1, 2025 as the common reference date. The outcome was estimated time from peak height velocity (PHV), expressed in years. Negative values indicate time before estimated PHV and positive values indicate time after estimated PHV. This measure is an anthropometric estimate of maturation rather than a direct measurement of biological age.

    Time frame: Baseline

  2. Functional Movement Screen Total Score

    Functional movement quality was assessed using the Functional Movement Screen (FMS). Seven movement patterns were scored from 0 to 3: deep squat, hurdle step, in-line lunge, shoulder mobility, active straight-leg raise, trunk stability push-up, and rotary stability. A score of 3 indicates performance meeting the standard criteria, 2 indicates compensatory movement, 1 indicates inability to meet the criteria, and 0 indicates pain. For bilateral items, the lower of the two side scores contributed to the total. The seven item scores were summed to give a total score from 0 to 21 points. Higher scores indicate better functional movement quality.

    Time frame: Baseline

  3. Final Running Speed in the 30-15 Intermittent Fitness Test

    Intermittent running performance was assessed using the 30-15 Intermittent Fitness Test on a 40-m shuttle course. The test consisted of 30-second running stages separated by 15-second recovery periods. Running speed started at 8 km/h and increased by 0.5 km/h at each stage. Participants followed audio signals until they could no longer maintain the required pace or continue the test. The outcome was the speed of the last completed stage, recorded in kilometers per hour (km/h). Higher values indicate better intermittent running performance.

    Time frame: Baseline

  4. Pro-Agility Test Completion Time

    Change-of-direction performance was assessed using the Pro-Agility Test. Markers were placed 5 yards (4.57 m) to either side of the central starting line. From the central line, the participant moved to and touched the right marker, then the left marker, and returned through the central line. Completion time was measured using a photocell timing system at the central line and recorded in seconds. Lower values indicate faster completion and better change-of-direction performance.

    Time frame: Baseline

  5. Hamstring Isometric Strength

    Hamstring isometric strength was assessed using an Active Force 2 digital handheld dynamometer. The participant lay prone with the knee flexed to approximately 90 degrees and performed three maximal isometric knee-flexion contractions lasting approximately 3 to 5 seconds each, with 30 seconds of rest between trials. The highest force recorded across the three trials was used as the outcome and expressed in newtons (N). Higher values indicate greater hamstring isometric strength.

    Time frame: Baseline

  6. Quadriceps Isometric Strength

    Quadriceps isometric strength was assessed using an Active Force 2 digital handheld dynamometer. The participant sat with the hip and knee flexed to approximately 90 degrees and performed three maximal isometric knee-extension contractions lasting approximately 3 to 5 seconds each, with 30 seconds of rest between trials. The highest force recorded across the three trials was used as the outcome and expressed in newtons (N). Higher values indicate greater quadriceps isometric strength.

    Time frame: Baseline

  7. Number of Balance Errors in the Flamingo Balance Test

    Static balance was assessed using the Flamingo Balance Test. The participant maintained a single-leg stance for \[CONFIRMED TEST DURATION\]. Touching the ground with the non-supporting foot, moving the supporting foot, or losing balance was counted as an error. The total number of balance errors during the assessment was recorded as a count. Lower values indicate better static balance.

    Time frame: Baseline

  8. Mean Seated Medicine Ball Chest Pass Distance

    Upper-body explosive performance was assessed using a seated chest pass with a 3-kg medicine ball. The participant sat with the knees extended and the back, shoulders, and head against a wall. The ball was thrown as far as possible from chest level using both hands while maintaining contact with the wall. After warm-up and practice attempts, four valid throws were performed with 30 to 45 seconds of rest between throws. The arithmetic mean of the four throwing distances was recorded in meters (m). Higher values indicate better throwing performance.

    Time frame: Baseline

  9. Right Anterior Normalized Reach Score on the Y Balance Test

    Dynamic balance was assessed using the Y Balance Test with the right leg as the stance limb. After practice attempts, three valid reaches were recorded in the anterior direction. The greatest valid reach distance was divided by the length of the right lower limb and multiplied by 100. Lower-limb length was measured from the anterior superior iliac spine to the medial malleolus. The outcome was expressed as a percentage of limb length. Higher values indicate greater reach relative to limb length.

    Time frame: Baseline

  10. Right Posteromedial Normalized Reach Score on the Y Balance Test

    Dynamic balance was assessed using the Y Balance Test with the right leg as the stance limb. After practice attempts, three valid reaches were recorded in the posteromedial direction. The greatest valid reach distance was divided by the length of the right lower limb and multiplied by 100. Lower-limb length was measured from the anterior superior iliac spine to the medial malleolus. The outcome was expressed as a percentage of limb length. Higher values indicate greater reach relative to limb length.

    Time frame: Baseline

  11. Right Posterolateral Normalized Reach Score on the Y Balance Test

    Dynamic balance was assessed using the Y Balance Test with the right leg as the stance limb. After practice attempts, three valid reaches were recorded in the posterolateral direction. The greatest valid reach distance was divided by the length of the right lower limb and multiplied by 100. Lower-limb length was measured from the anterior superior iliac spine to the medial malleolus. The outcome was expressed as a percentage of limb length. Higher values indicate greater reach relative to limb length.

    Time frame: Baseline

  12. Right Composite Score on the Y Balance Test

    Dynamic balance was assessed using the Y Balance Test with the right leg as the stance limb. The greatest valid reach distance from three trials in each of the anterior, posteromedial, and posterolateral directions was used. The three distances were summed, divided by three times the length of the right lower limb, and multiplied by 100. Lower-limb length was measured from the anterior superior iliac spine to the medial malleolus. The composite score was expressed as a percentage of limb length. Higher values indicate greater overall reach relative to limb length.

    Time frame: Baseline

  13. Left Anterior Normalized Reach Score on the Y Balance Test

    Dynamic balance was assessed using the Y Balance Test with the left leg as the stance limb. After practice attempts, three valid reaches were recorded in the anterior direction. The greatest valid reach distance was divided by the length of the left lower limb and multiplied by 100. Lower-limb length was measured from the anterior superior iliac spine to the medial malleolus. The outcome was expressed as a percentage of limb length. Higher values indicate greater reach relative to limb length.

    Time frame: Baseline

  14. Left Posteromedial Normalized Reach Score on the Y Balance Test

    Dynamic balance was assessed using the Y Balance Test with the left leg as the stance limb. After practice attempts, three valid reaches were recorded in the posteromedial direction. The greatest valid reach distance was divided by the length of the left lower limb and multiplied by 100. Lower-limb length was measured from the anterior superior iliac spine to the medial malleolus. The outcome was expressed as a percentage of limb length. Higher values indicate greater reach relative to limb length.

    Time frame: Baseline

  15. Left Posterolateral Normalized Reach Score on the Y Balance Test

    Dynamic balance was assessed using the Y Balance Test with the left leg as the stance limb. After practice attempts, three valid reaches were recorded in the posterolateral direction. The greatest valid reach distance was divided by the length of the left lower limb and multiplied by 100. Lower-limb length was measured from the anterior superior iliac spine to the medial malleolus. The outcome was expressed as a percentage of limb length. Higher values indicate greater reach relative to limb length.

    Time frame: Baseline

  16. Left Composite Score on the Y Balance Test

    Dynamic balance was assessed using the Y Balance Test with the left leg as the stance limb. The greatest valid reach distance from three trials in each of the anterior, posteromedial, and posterolateral directions was used. The three distances were summed, divided by three times the length of the left lower limb, and multiplied by 100. Lower-limb length was measured from the anterior superior iliac spine to the medial malleolus. The composite score was expressed as a percentage of limb length. Higher values indicate greater overall reach relative to limb length.

    Time frame: Baseline

07

Study locations

1 site
  • Alanya Alaaddin Keykubat University
    Antalya, Alanya 07400, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No — Individual participant data (IPD) will not be shared due to ethical and legal restrictions related to the protection of personal data. Although data will be de-identified, there remains a potential risk of re-identification. Therefore, all data will be stored securely and used solely for research purposes in accordance with institutional and national data protection regulations.

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from May 2025 to primary completion in May 2025, 0 months.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 15, 2026
First posted
Nov 5, 2026
StartActual
May 15, 2025
Primary completionActual
May 16, 2025
CompletionActual
May 15, 2026
Last update
Nov 5, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 5, 2026
Show all 1 update
  1. Nov 5, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07920146
Lead sponsor
Alanya Alaaddin Keykubat University
Responsible party
Ayça Araci (Assitant Prof., Alanya Alaaddin Keykubat University) — Principal investigator
First posted
Nov 5, 2026
Start date
May 15, 2025
Primary completion
May 16, 2025
Completion
May 15, 2026
Last update
Nov 5, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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